Bhagat, Lakshmi (Brookline, MA, US)
Pandey, Rajendra K. (Framingham, MA, US)
Yu, Dong (Westboro, MA, US)
Agrawal, Sudhir (Shrewsbury, MA, US)
2. The immunostimulatory nucleic acid of claim 1, wherein the oligonucleotide sequence is from about 12 to about 50 nucleotides in length.
3. The immunostimulatory nucleic acid of claim 1, wherein the oligonucleotide sequence is from about 12 to about 26 nucleotides in length.
4. The immunostimulatory nucleic acid of claim 1, wherein the oligonucleotide sequence forms a 3′-end stem loop secondary structure.
5. The immunostimulatory nucleic acid of claim 1, wherein the oligonucleotide sequence has a palindromic or complementary sequence at the 3′-end.
6. The immunostimulatory nucleic acid of claim 1 selected from the group consisting of SEQ ID NOS: 2, 3, 4, 9, 12, 13, 14, 18, 19, 20, 21, 24, 25, 26, 27, 28, 29, 30, 32, 33, 34, 35, 36, 60, 61, 62, 63 and 65.
7. A immunostimulatory nucleic acid having reduced immunostimulatory activity comprising an oligonucleotide sequence containing at least one dinucleotide selected from the group consisting of CpG, C*pG, C*pG* and CpG*, wherein C is cytidine or 2′-deoxycitidine, G is guanosine or 2′-deoxyguanosine, C* is 2′-deoxythymidine, 1-(2′-deoxy-β-D-ribofuranosyl)-2-oxo-7-deaza-8-methyl-purine, 2′-dideoxy-5-halocytosine, 2′ dideoxy-5-nitrocytosine, arabinocytidine, 2′-deoxy-2′-substitutedarabinocytidine, 2′-O-substituted arabinocytidine, 2′-deoxy-5-hydroxycytidine, 2′-deoxy-N4-alkyl-cytidine, 2′-deoxy-4-thiouridine, or other non-natural pyrimidine nucleosides, G* is 2′-deoxy-7-deazaguanosine, 2′-deoxy-6-thioguanosine, arabinoguanosine, 2′-deoxy-2′substituted-arabinoguanosine, 2′-O-substituted-arabinoguanosine, 2′-deoxyinosine, or other non-natural purine nucleoside, p is an internucleoside linkage selected from the group consisting of phosphodiester, phosphorothioate, and phosphorodithioate, and wherein the oligonucleotide sequence has a secondary structure at the 5′-end of the oligonucleotide sequence.
8. The immunostimulatory nucleic acid of claim 7, wherein the oligonucleotide sequence is from about 12 to about 50 nucleotides in length.
9. The immunostimulatory nucleic acid of claim 7, wherein the oligonucleotide sequence is from about 12 to about 26 nucleotides in length.
10. The immunostimulatory nucleic acid of claim 7, wherein the oligonucleotide sequence forms a 5′-end stem loop secondary structure.
11. The immunostimulatory nucleic acid of claim 7, wherein the oligonucleotide sequence has a palindromic or complementary sequence at the 5′-end.
12. The immunostimulatory nucleic acid of claim 7 selected from the group consisting of SEQ ID NOS: 5, 6, 7, 10, 15, 16 and 17.
13. A method of reducing or eliminating the immunostimulatory activity of an oligonucleotide having at least one dinucleotide selected from the group consisting of CpG, C*pG, C*pG* and CpG*, wherein C is cytidine or 2′-deoxycitidine, G is guanosine or 2′-deoxyguanosine, C* is 2′-deoxythymidine, 1-(2′-deoxy-β-D-ribofuranosyl)-2-oxo-7-deaza-8-methyl-purine, 2′ dideoxy-5-halocytosine, 2′-dideoxy-5-nitrocytosine, arabinocytidine, 2′-deoxy-2′-substitutedarabinocytidine, 2′-O-substituted arabinocytidine, 2′-deoxy-5-hydroxycytidine, 2′-deoxy-N4-alkyl-cytidine, 2′-deoxy-4-thiouridine, or other non-natural pyrimidine nucleosides, G* is 2′-deoxy-7-deazaguanosine, 2′-deoxy-6-thioguanosine, arabinoguanosine, 2′-deoxy-2′substituted-arabinoguanosine, 2′-O-substituted-arabinoguanosine, 2′-deoxyinosine, or other non-natural purine nucleoside, and p is an internucleoside linkage selected from the group consisting of phosphodiester, phosphorothioate, and phosphorodithioate, the method comprising introducing at the 5′-end of the oligonucleotide a nucleic acid sequence comprising a secondary structure.
14. The method of claim 13, wherein the secondary structure is a stem-loop structure.
15. The method of claim 13, wherein the secondary structure is hydrogen bonding to a palindromic or complementary sequence.
16. A pharmaceutical composition comprising the immunostimulatory nucleic acid of claim 1 and a pharmaceutically acceptable carrier.
17. A pharmaceutical composition comprising the immunostimulatory nucleic acid of claim 7 and a pharmaceutically acceptable carrier.
18. An immunostimulatory nucleic acid comprising at least two oligonucleotides, wherein the immunostimulatory nucleic acid has a secondary structure and the immunostimulatory nucleic acid comprises the general structure of:
Domain A-Domain B-Domain C, (I) wherein Domain A may be 5′-3′ or 3′-5′ or 2′-5′ DNA, RNA, RNA-DNA, DNA-RNA having or not having a palindromic or self-complementary domain containing or not containing at least one dinucleotide selected from the group consisting of CpG, C*pG, C*pG* and CpG*, wherein C is cytidine or 2′-deoxycitidine, G is guanosine or 2′-deoxyguanosine, C* is 2′-deoxythymidine, 1-(2′-deoxy-β-D-ribofuranosyl)-2-oxo-7-deaza-8-methyl-purine, 2′ dideoxy-5-halocytosine, 2′-dideoxy-5-nitrocytosine, arabinocytidine, 2′-deoxy-2′-substitutedarabinocytidine, 2′-O-substituted arabinocytidine, 2′-deoxy-5-hydroxycytidine, 2′-deoxy-N4-alkyl-cytidine, 2′-deoxy-4-thiouridine, or other non-natural pyrimidine nucleosides, G*is 2′ deoxy-7-deazaguanosine, 2′-deoxy-6-thioguanosine, arabinoguanosine, 2′-deoxy-2′-substituted-arabinoguanosine, 2′-O-substituted-arabinoguanosine, 2′-deoxyinosine, or other non-natural purine nucleoside, and p is an internucleoside linkage selected from the group consisting of phosphodiester, phosphorothioate, and phosphorodithioate, Domain B is a linker joining Domains A and C that may be a 3′-‘5’ linkage, a 2′-5′ linkage, a 3′-3′ linkage, a phosphate group, a nucleoside, or a non-nucleoside linker that may be aliphatic, aromatic, aryl, cyclic, chiral, achiral, a peptide, a carbohydrate, a lipid, a fatty acid, mono- tri- or hexapolyethylene glycol, or a heterocyclic moiety and Domain C may be 5′-3′ or 3′-5′, 2′-5′ DNA, RNA, RNA-DNA, DNA-RNA Poly I-Poly C having or not having a palindromic or self-complementary sequence, which can or cannot have a dinucleotide selected from the group consisting of CpG, C*pG, C*pG* and CpG*, wherein C is cytidine or 2′deoxycitidine, G is guanosine or 2′ deoxyguanosine, C* is 2′-deoxythymidine, 1-(2′-deoxy-β-D-ribofuranosyl)-2-oxo-7-deaza-8-methyl-purine, 2′-dideoxy-5-halocytosine, 2′-dideoxy-5-nitrocytosine, arabinocytidine, 2′-deoxy-2′-substituted arabinocytidine, 2′-O-substituted arabinocytidine, 2′-deoxy-5-hydroxycytidine, 2′-deoxy-N4-alkyl-cytidine, 2′-deoxy-4-thiouridine, or other non-natural pyrimidine nucleosides, G* is 2′ deoxy-7-deazaguanosine, 2′-deoxy-6-thioguanosine, arabinoguanosine, 2′-deoxy-2′substituted-arabinoguanosine, 2′-O-substituted-arabinoguanosine, 2′-deoxyinosine, or other non-natural purine nucleoside, p is an internucleoside linkage selected from the group consisting of phosphodiester, phosphorothioate.
19. (Canceled).
20. (Canceled).
21. An immunostimulatory nucleic acid according to claim 18, wherein Domain A is selected from the group consisting of SEQ ID NO. 37, 38, 42 and 64; Domain B is at least one C3 linker; and Domain C is selected from the group consisting of SEQ ID NO. 55, 67, 68, 71 and 73, and wherein the 3′ end of Domain A and the 5′ end of Domain C are linked to the linker.
22. An immunostimulatory nucleic acid according to claim 18, wherein Domain A is selected from the group consisting of SEQ ID NO. 39, 40, 41, 44 and 64; Domain B is at least one C3 linker; and Domain C is selected from the group consisting of SEQ ID NO. 47, 48, 49, 50, 51, 52, 53, 54, 59 and 72, and wherein the 3′ end of Domain A and the 3′ end of Domain C are linked to the linker.
23. An immunostimulatory nucleic acid according to claim 18, wherein Domain A comprises the sequence of SEQ ID NO. 39; Domain B is a tetraethyleneglycol linker; and Domain C is selected from the group consisting of SEQ ID NO. 47 and 50, and wherein the 3′ end of Domain A and the 3′ end of Domain C are linked to the linker.
24. An immunostimulatory nucleic acid according to claim 18, wherein Domain A comprises the sequence of SEQ ID NO. 39; Domain B is a hexaethyleneglycol linker; and Domain C is selected from the group consisting of SEQ ID NO. 47 and 50, and wherein the 3′ end of Domain A and the 3′ end of Domain C are linked to the linker.
25. An immunostimulatory nucleic acid according to claim 18, wherein Domain A comprises the sequence of SEQ ID NO. 66; Domain B is a glycerol; and Domain C is selected from the group consisting of SEQ ID NO. 47, 72, 74, 75 and 76, and wherein the 3′ end of Domain A and the 3′ end of Domain C are linked to the glycerol moiety.
RELATED APPLICATIONS
This application claims the benefit of U.S. Provisional Application No. 60/477,608, filed Jun. 11, 2003, U.S. Provisional Application No. 60/499,038 filed Aug. 29, 2003, and U.S. Provisional Application No. 60/504,279 filed Sep. 18, 2003, which are incorporated by reference in their entirety.
BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to the fields of molecular biology, immunology and medicine. More specifically, the invention relates to immunostimulatory oligonucleotides and therapeutic uses thereof.
2. Summary of the Related Art
The immune system has evolved to specifically recognize DNA that contains an unmethylated CpG dinucleotide motif, which commonly occurs in the DNA of pathogens such as bacteria and viruses. As a result, unmethylated CpG-containing DNA is potent stimulator of the vertebrate immune system. First reports of immune stimulation by DNA came from studies using bacterial DNA and short fragments of DNA containing palindromic sequences, both of which were double-stranded structures with phosphodiester backbones Tokunaga, T., et al., ( J. Natl. Cancer Inst. 72: 955-962 (1984)) demonstrated potent anti-tumor activity for DNA isolated from Mycobacterium bovis BCG. Kataoka, T, et al., ( Jpn. J. Cancer Res. 83: 244-247 (1992)), Hartmann et al. ( European Journal of Immunology 33:1673-1641 (2003)), Marshall et al. Journal of Leukocyte Biology 73:781-792 (2003) showed a similar type of anti-tumor activity for synthetic oligodeoxynucleotides, the design of which was based on Mycobacterium bovis BCG cDNA sequences.
Sato, Y, et al., ( Science 273: 352-354 (1996)) showed the importance of CpG-containing DNA in the application of DNA vaccines (see also Gurunathan S., et al. ( Annu. Rev. Immunol. 18: 927-974 (2000)). Pisetsky, D. S., et al., (Mol. Biol. Rep. 18: 217-221 (1993)) and Krieg, A. M., et al., ( Nature 374: 546-549 (1995)) showed that DNA containing unmethylated CpG-dinucleotides in specific sequence contexts (CpG DNA) activated the vertebrate immune system, leading to proliferation of B cells and activation of macrophages, monocytes, NK cells, and dendritic cells. In response to CpG DNA activation, immune cells secrete a number of cytokines including IL-12, IFN-γ, INF-α, IL-6 and TNF-α and express several co-stimulatory molecules (for example, see Pisetsky, D. S., et al. and Krieg, A. M., et al., supra).
Kandimalla, E. R., et al., ( Curr. Opin. Mol. Ther. 4 122-129 (2002)) indicate that the presence and position of a CpG-dinucleotide and the sequences that flank it are critical for immunostimulatory activity. Agrawal, S., et al. ( Current Cancer Drug Targets 1: 197-209 (2001)) discloses significant effects due to ribose modifications in the flanking sequences of the CpG oligonucleotides. These effects depend on the position and nature of substituents, including 2′-O-methoxyethoxy and 2′- or 3′-O-methyl groups. Yu, D., et al. ( Bioorg. Med. Chem. 9: 2803-2808 (2001)) demonstrate that phosphate modifications can also increase or decrease immunostimulatory activity depending on their position. Yu D., et al. ( Bioorg. Med. Chem. Lett. 11: 2263-2267 (2001)) and Yu D., et al. ( Bioorg. Med. Chem. 11: 459-464 (2003)) disclose that activity can be increased by deletion of certain nucleobases. In addition Yu D., et al. ( Bioorg. Med. Chem. 11: 459-464 (2003)) disclose that immunostimulatory activity can be increased by substitution of certain flanking nucleotides with non-nucleotidic linkers.
Yu D., et al. ( Bioorg. Med. Chem. Lett. 10: 2585-2588 (2000)), Yu D., et al. ( Nucleic Acids Res. 30: 4460-4469 (2002)), Yu D., et al. ( Biochem. Biophys. Res. Commun. 297: 83-90 (2002)), Bhagat L., et al. ( Biochem. Biophys. Res. Commun. 300: 853-861 (2003)) and Kandimalla E. R., et al. ( Nucleic Acids Res. 31: 2393-2400 (2003) previously have shown that the 5′-terminus is involved in receptor recognition and that accessibility of this end is critical for activity. Kandimalla E. R., et al. ( Bioconj. Chem. 13: 966-974 (2002)) disclose loss of immunostimulatory activity following 5′-terminal conjugation of ligands larger than fluorescein or a 5′-5′ linked dinucleotide. As 3′-conjugation is without effect, changes in uptake cannot account for the results (Id.). However, there have not been any systematic studies to elucidate the role of secondary structure of DNA on the resulting immune response. The invention herein provides information on immunostimulation by immunostimulatory DNA with 5′- and 3′-hairpin loops or sticky ends that can form duplexes.
The ability of immunostimulatory DNA to induce Th1 cytokine production and promote CTL responses with enhanced immunoglobulin production has been used for treating a broad spectrum of disease indications including cancers, viral and bacterial infections, inflammatory disorders and as an adjuvant in immunotherapy. Thus, the benefits of improving or modulating immunostimulatory DNA activity are clear, and there remains a need in the art to develop improved immunostimulatory nucleic acids.
BRIEF SUMMARY OF THE INVENTION
The invention provides novel compositions of matter comprising immunostimulatory oligonucleotides with increased or decreased immunostimulatory properties. The invention also provides methods that enable the design of immunostimulatory oligonucleotides with increased or decreased immunostimulatory properties or with increased metabolic stability. The inventors have surprisingly discovered that the introduction of a secondary structure into the 3′-end or 5 ′-end of immunostimulatory oligonucleotides significantly impacts the immunostimulatory activity and stability of these oligonucleotides.
In a first aspect the invention provides an immunostimulatory nucleic acid. The immunostimulatory nucleic acid comprises an oligonucleotide sequence containing at least one dinucleotide selected from the group consisting of CpG, C*pG, C*pG* and CpG*, wherein C is cytidine or 2′-deoxycytidine, G is guanosine or 2′ deoxyguanosine, C* is cytidine, 2′-deoxythymidine, 1-(2′-deoxy-β-D-ribofuranosyl)-2-oxo-7-deaza-8-methyl-pur ine, 2′-dideoxy-5-halocytosine, 2′-dideoxy-5-nitrocytosine, arabinocytidine, 2′-deoxy-2′-substitutedarabinocytidine, 2′-O-substituted arabinocytidine, 2′-deoxy-5-hydroxycytidine, 2′-deoxy-N4-alkyl-cytidine, 2′-deoxy-4-thiouridine, or other pyrimidine nucleoside analogs, G* is 2′ deoxy-7-deazaguanosine, 2′-deoxy-6-thioguanosine, arabinoguanosine, 2′-deoxy-2′substituted-arabinoguanosine, 2′-O-substituted-arabinoguanosine, 2′-deoxyinosine, or other purine nucleoside analogs, and p is an internucleoside linkage selected from the group consisting of phosphodiester, phosphorothioate, and phosphorodithioate. In certain preferred embodiments the oligonucleotide sequence has a secondary structure at the 3′-end of the oligonucleotide sequence. In certain preferred embodiments, the immunostimulatory dinucleotide is not CpG.
In some embodiments, the immunostimulatory nucleic acid is from about 2 to about 50 nucleotides in length. In certain embodiments the immunostimulatory nucleic acid is from about 12 to about 26 nucleotides in length. In some embodiments, the oligonucleotides each have from about 3 to about 35 nucleoside residues, preferably from about 4 to about 30 nucleoside residues, more preferably from about 4 to about 20 nucleoside residues. In some embodiments, the oligonucleotides have from about 5 to about 18 or from about 5 to about 14, nucleoside residues. As used herein, the term “about” implies that the exact number is not critical. Thus, the number of nucleoside residues in the oligonucleotides is not critical, and oligonucleotides having one or two fewer nucleoside residues, or from one to several additional nucleoside residues are contemplated as equivalents of each of the embodiments described above. In some embodiments, one or more of the oligonucleotides have 11 nucleotides.
In certain embodiments, the immunostimulatory nucleic acid has a 3′-end stem loop secondary structure. In some embodiments, the immunostimulatory nucleic acid has a secondary structure at the 3′-end by way of hydrogen bonding with a complementary sequence. In certain embodiments, the immunostimulatory nucleic acid is selected from the group consisting of SEQ ID NOS: 2, 3, 4, 9, 12, 13, 14, 18, 19, 20, 21, 24, 25, 26, 27, 28, 29, 30, 32, 33, 34, 35, 36, 37 and 38.
In a second aspect, the invention provides a nucleic acid having reduced immunostimulatory activity. In this aspect the nucleic acid comprises an oligonucleotide sequence containing at least one dinucleotide selected from the group consisting of CpG, C*pG, C*pG* and CpG*, wherein C is cytidine or 2′-deoxycytidine, G is guanosine or 2′-deoxyguanosine, C* is 2′-deoxythymidine, 1-(2′-deoxy-β-D-ribofuranosyl)-2-oxo-7-deaza-8-methyl-pur ine, 2′-dideoxy-5-halocytosine, 2′-dideoxy-5-nitrocytosine, arabinocytidine, 2′-deoxy-2′-substituted arabinocytidine, 2′-O-substituted arabinocytidine, 2′-deoxy-5-hydroxycytidine, 2′-deoxy-N4-alkyl-cytidine, 2′-deoxy-4-thiouridine, or other pyrimidine nucleoside analogs; G* is 2′deoxy-7-deazaguanosine, 2′-deoxy-6-thioguanosine, arabinoguanosine, 2′-deoxy-2′substituted-arabinoguanosine, 2′-O-substituted-arabinoguanosine, 2′-deoxyinosine, or other purine nucleoside analogs, and p is an internucleoside linkage selected from the group consisting of phosphodiester, phosphorothioate, and phosphorodithioate. In certain preferred embodiments the oligonucleotide sequence has a secondary structure at the 3′-end of the oligonucleotide sequence. In certain preferred embodiments, the immunostimulatory dinucleotide is not CpG.
In some embodiments, the immunostimulatory nucleic acid is an oligonucleotide sequence from about 2 to about 50 nucleotides in length. In certain embodiments the immunostimulatory nucleic acid is an oligonucleotide sequence from about 12 to about 26 nucleotides in length.
In certain embodiments the nucleic acid having reduced immunostimulatory activity forms a 5′-end stem loop secondary structure. In some embodiments, the nucleic acid having reduced immunostimulatory activity has a secondary structure at the 5′-end by way of hydrogen bonding with a complementary sequence. In certain embodiments the nucleic acid having reduced immunostimulatory activity is selected from the group consisting of SEQ ID NOS: 5, 6, 7, 10, 15, 16 and 17.
In a third aspect the invention provides an immunostimulatory nucleic acid comprising at least two oligonucleotides, wherein the immunostimulatory nucleic acid has a secondary structure. In this aspect, the immunostimulatory nucleic acid comprises a structure as detailed in formula (I).
Domain A-Domain B-Domain C (I)
Domains may be from about 2 to about 12 nucleotides in length. Domain A may be 5′-3′ or 3′-5′ or 2′-5′ DNA, RNA, RNA-DNA, DNA-RNA having or not having a palindromic or self-complementary domain containing or not containing at least one dinucleotide selected from the group consisting of CpG, C*pG, C*pG* and CpG*, wherein C is cytidine or 2′-deoxycytidine, G is guanosine or 2′ deoxyguanosine, C* is 2′-deoxythymidine, 1-(2′-deoxy-β-D-ribofuranosyl)-2-oxo-7-deaza-8-methyl-pur ine, 2′-dideoxy-5-halocytosine, 2′-dideoxy-5-nitrocytosine, arabinocytidine, 2′-deoxy-2′-substitutedarabinocytidine, 2′-O-substituted arabinocytidine, 2′-deoxy-5-hydroxycytidine, 2′-deoxy-N4-alkyl-cytidine, 2′-deoxy-4-thiouridine, or other pyrimidine nucleoside analogs, G- is guanosine or 2′ deoxyguanosine, 2′ deoxy-7-deazaguanosine, 2′-deoxy-6-thioguanosine, arabinoguanosine, 2′-deoxy-2′substituted-arabinoguanosine, 2′-O-substituted-arabinoguanosine, 2′-deoxyinosine, or other purine nucleoside analogs. In certain embodiments, Domain A will have more than one dinucleotide selected from the group consisting of CpG, C*pG, C*pG* and CpG*.
Domain B, as depicted by an “X” below, is a linker joining Domains A and C that may be a 3′-′5′ linkage, a 2′-5′ linkage, a 3′-3′ linkage, a phosphate group, a nucleoside, or a non-nucleoside linker that may be aliphatic, aromatic, aryl, cyclic, chiral, achiral, a peptide, a carbohydrate, a lipid, a fatty acid, mono- tri- or hexapolyethylene glycol, or a heterocyclic moiety. In some embodiments, Domain B is preferably a non-nucleotidic linker connecting oligonucleotides of Domain A and Domain C, which are referred to as “immunomers”.
Domain C may be 5′-3′ or 3′-5′, 2′-5′ DNA, RNA, RNA-DNA, DNA-RNA Poly I-Poly C having or not having a palindromic or self-complementary sequence, which can or cannot have a dinucleotide selected from the group consisting of CpG, C*pG, C*pG* and CpG*, wherein C is cytidine or 2′-deoxycytidine, G is guanosine or 2′-deoxyguanosine, C* is 2′-deoxythymidine, 1-(2′-deoxy-β-D-ribofuranosyl)-2-oxo-7-deaza-8-methyl-pur ine, arabinocytidine, 2′-deoxy-2′-substituted arabinocytidine, 2′-O-substituted arabinocytidine, 2′-deoxy-5-hydroxycytidine, 2′-deoxy-N4-alkyl-cytidine, 2′-deoxy-4-thiouridine, or other pyrimidine nucleoside analogs, G* is 2′-deoxy-7-deazaguanosine, 2′-deoxy-6-thioguanosine, arabinoguanosine, 2′-deoxy-2′substituted-arabinoguanosine, 2′-O-substituted-arabinoguanosine, 2′-deoxyinosine, or other purine nucleoside analogs, and p is an internucleoside linkage selected from the group consisting of phosphodiester, phosphorothioate, and phosphorodithioate. In certain preferred embodiments, the immunostimulatory dinucleotide is not CpG. In certain preferred embodiments, Domain C does not have the dinucleotide CpG, C*pG, C*pG*, or CpG*.
In some embodiments, the oligonucleotides contained in formula (I) are from about 2 to about 50 nucleotides in length. In certain embodiments the oligonucleotides contained in formula (I) are from about 12 to about 26 nucleotides in length.
By way of non-limiting example, in certain embodiments of this aspect the immunostimulatory nucleic acid will have a structure as detailed in formula (II).
As one skilled in the art would recognize, there is a secondary structure element in the 3′ end of the molecule in the form of an intramolecular stem-loop.
By way of non-limiting example, in certain embodiments of this aspect the immunostimulatory nucleic acid will have a structure as detailed in formula (III).
The structure depicted in formula (III) is referred to herein as a “terminal dimmer,” since the 3′ ends of the two molecules are blocked because the sequences of the two 3′ ends are complementary allowing for intermolecular hydrogen bonding. In addition, domains A and A′ may or may not be identical, domains B and B′ may or may not be identical and domains C and C′ may or may not be identical.
By way of non-limiting example, in certain embodiments of this aspect the immunostimulatory nucleic acid will have a structure as detailed in formula (IV).
As would be recognized by one skilled in the art, the 3′ end of the depicted molecule has a secondary structure because the complementary sequence of its 3′ end is hydrogen bonded to this region.
In certain embodiments, the immunostimulatory nucleic acids of the invention have sequence selected from the group consisting of SEQ ID NOS: 1-38. In some embodiments, the immunostimulatory nucleic acids of the invention have a sequence selected from the group consisting of SEQ ID NOS: 39-68.
In a fourth aspect, the invention provides a method for reducing or eliminating the immunostimulatory activity of an oligonucleotide. The method comprises introducing at the 5′-end of the oligonucleotide a nucleic acid sequence comprising a secondary structure. In some embodiments of this aspect, the secondary structure is a stem-loop structure. In certain embodiments of this aspect, the secondary structure is obtained by hydrogen bonding a complementary sequence to the 5′-end of the oligonucleotide sequence.
In a fifth aspect, the invention provides a method for increasing the stability of an immunostimulatory oligonucleotide. The method comprises introducing at the 3′-end of the immunostimulatory oligonucleotide a nucleic acid sequence comprising a secondary structure. In some embodiments of this aspect, the secondary structure is a stem-loop structure. In certain embodiments of this aspect, the secondary structure is obtained by hydrogen bonding a complementary sequence to the 3′-end of the oligonucleotide sequence.
In a sixth aspect, the invention provides a method for modulating the immunostimulatory activity of an immunostimulatory oligonucleotide. The method comprises introducing at the 3′-end or the 5′-end of the immunostimulatory oligonucleotide a nucleic acid sequence comprising a secondary structure. In some embodiments of this aspect, the secondary structure is a stem-loop structure. In certain embodiments of this aspect, the secondary structure is obtained by hydrogen bonding a complementary sequence to the 3′-end or 5′-end of the oligonucleotide sequence.
In a seventh aspect the invention provides pharmaceutical compositions. These compositions comprise any one of the compositions disclosed in the first, second, third, fourth, fifth and sixth aspects of the invention either alone or in combination and a pharmaceutically acceptable carrier.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1A is a schematic representation showing cell proliferation induced by oligos 1, 2, and 5 in BALB/c mouse spleen cell cultures at a concentration of 1.0 μg/mL.
FIG. 1B is a schematic representation showing splenomegaly induced by oligos 1, 2, and 5 at a dose of 5 mg/kg administered intraperitoneally to BALB/c mice.
FIG. 2 is a schematic representation showing induction of cytokines IL-12 and IL-6 in BALB/c mouse spleen cell cultures after 24 hours of incubation with oligonucleotides 1-7 at a concentration of 3 μg/mL.
FIG. 3 is a schematic representation showing induction of cytokines IL-12 and IL-6 in BALB/c mouse spleen cell cultures after 24 hours of incubation with oligonucleotides 8-10 at a concentration of 3 μg/mL.
FIG. 4 is a representation showing activation of the NF-κB pathway in J774 macrophages after 1 hr stimulation with 10 μg/mL of oligos 1-8. M stands for control treated with media and C is cells treated with a non-CpG oligo.
FIG. 5 is a schematic representation showing induction of cytokines IL-12 and IL-6 in J774 macrophage cell cultures at a concentration of oligos 1-7 of 10 μg/mL. M stands for control treated with PBS. ND denotes not detected.
FIG. 6 is a schematic representation showing induction of interferon α (IFN-α) in plasmacytoid dendritic cells after exposure to oligos 11, 12, 14, 15 and 17 at 10 μg/ml.
FIG. 7 is a schematic representation showing induction of interferon α (IFN-α) in plasmacytoid dendritic cells after exposure to oligos 18, 19, 20, and 21 at 10 μg/ml.
FIG. 8 is a schematic representation showing induction of interferon α (IFN-α) in plasmacytoid dendritic cells after exposure to oligos 41, 44, and 45 at 10 μg/ml.
FIG. 9 is a synthetic scheme for the parallel synthesis of immunomers of the invention. DMTr=4,4′-dimethoxytrityl; CE=cyanoethyl.
FIG. 10 depicts a group of representative small molecule linkers suitable for linear synthesis of immumomers of the invention.
FIG. 11 is a synthetic scheme for the linear synthesis of immunomers of the invention. DMTr=4,4′-dimethoxytrityl; CE=cyanoethyl.
FIG. 12 depicts a group of representative small molecule linkers suitable for parallel synthesis of immunomers of the invention.
FIG. 13 Self-stabilized CpG DNAs induce (A) IFN-α secretion by human pDCs and (B) human B-cell proliferation in cultures. (A) pDCs were isolated from human PBMCs obtained from 5-8 healthy donors and stimulated with 10 μg/mL of CpG DNAs for 24 hr and the supernatants were assayed for IFN-α secretion by ELISA. (B) B cells were isolated from human PBMCs obtained from 4-7 healthy donors, stimulated with 1 μg/mL of CpG DNAs for 72 hr, and [ 3 H]-thymidine uptake was measured. Symbols represent data obtained with each donor and plus sign represents average value of all donors in both the panels.
FIG. 14 CpG DNA concentration dependence of human B cell proliferation. B cells were isolated from human PBMCs obtained from 4-6 healthy donors, stimulated with different concentrations of CpG DNAs for 72 hr. Data shown are average±SD.
FIG. 15 (A) The presence of a CpG motif and secondary structure are required for induction of IFN-α secretion by human pDCs. Data shown are average±SD of 6-8 human donors at a concentration 10 μg/mL of CpG DNA. (B) Human B-cell proliferation requires the presence of a CpG stimulatory motif but not a secondary structure in DNA. Data shown are average±SD of 5-8 donors at a concentration of 1 μg/mL of CpG DNA.
FIG. 16 Effect of 2′-O-methylribonucleotide segment in hairpin secondary structure on (A) IFN-α secretion by human pDCs and (B) human B-cell proliferation. Data shown are average±SD of 6-8 human donors at a concentration 10 μg/mL of CpG DNA in pDC cultures and 5-8 donors at a concentration of 1 μg/mL of CpG DNA in B cell cultures.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
The invention provides novel compositions of matter comprising immunostimulatory oligonucleotides with increased or decreased immunostimulatory properties. The invention also provides methods that enable the design of immunostimulatory oligonucleotides with increased or decreased immunostimulatory properties or with increased metabolic stability. The inventors have surprisingly discovered that the introduction of a secondary structure into the 3′-end or 5′-end of immunostimulatory oligonucleotides significantly impacts the immunostimulatory activity and stability of these oligonucleotides.
The issued patents, patent applications, and references that are cited herein are hereby incorporated by reference to the same extent as if each was specifically and individually indicated to be incorporated by reference. In the event of inconsistencies between any teaching of any reference cited herein and the present specification, the latter shall prevail for purposes of the invention.
In a first aspect the invention provides an immunostimulatory nucleic acid. The immunostimulatory nucleic acid comprises an oligonucleotide sequence containing at least one dinucleotide selected from the group consisting of CpG, C*pG, C*pG* and CpG*, wherein C is cytidine or 2′-deoxycytidine, G is guanosine or 2′ deoxyguanosine, C* is 2′-deoxythymidine, 1-(2′-deoxy-β-D-ribofuranosyl)-2-oxo-7-deaza-8-methyl-pur ine, 2′-dideoxy-5-halocytosine, 2′-dideoxy-5-nitrocytosine arabinocytidine, 2′-deoxy-2′-substituted arabinocytidine, 2′-O-substituted arabinocytidine, 2′-deoxy-5-hydroxycytidine, 2′-deoxy-N4-alkyl-cytidine, 2′-deoxy-4-thiouridine, or other pyrimidine nucleoside analogs, G* is 2′-deoxy-7-deazaguanosine, 2′-deoxy-6-thioguanosine, arabinoguanosine, 2′-deoxy-2′substituted-arabinoguanosine, 2′-O-substituted-arabinoguanosine, 2′-deoxyinosine, or other purine nucleoside analogs, and p is an internucleoside linkage selected from the group consisting of phosphodiester, phosphorothioate, and phosphorodithioate and wherein the oligonucleotide sequence has a secondary structure at the 3′-end of the oligonucleotide sequence. In certain preferred embodiments, the immunostimulatory dinucleotide is not CpG.
In some embodiments, the immunostimulatory nucleic acid is from about 2 to about 50 nucleotides in length. In certain embodiments the immunostimulatory nucleic acid is from about 12 to about 26 nucleotides in length. In some embodiments, the oligonucleotides each have from about 3 to about 35 nucleoside residues, preferably from about 4 to about 30 nucleoside residues, more preferably from about 4 to about 20 nucleoside residues. In some embodiments, the oligonucleotides have from about 5 to about 18, or from about 5 to about 14, nucleoside residues. As used herein, the term “about” implies that the exact number is not critical. Thus, the number of nucleoside residues in the oligonucleotides is not critical, and oligonucleotides having one or two fewer nucleoside residues, or from one to several additional nucleoside residues are contemplated as equivalents of each of the embodiments described above. In some embodiments, one or more of the oligonucleotides have 11 nucleotides.
In certain embodiments, the immunostimulatory nucleic acid has a 3′-end stem loop secondary structure. In some embodiments, the immunostimulatory nucleic acid has a secondary structure at the 3′-end by way of hydrogen bonding with a complementary sequence. In certain embodiments, the immunostimulatory nucleic acid is selected from the group consisting of SEQ ID NOS: 2, 3, 4, 9, 12, 13, 14, 18, 19, 20, 21, 24, 25, 26, 27, 28, 29, 30, 32, 33, 34, 35, 36, 37 and 38.
For purposes of the invention, the term “oligonucleotide” refers to a polynucleoside formed from a plurality of linked nucleoside units. Such oligonucleotides can be obtained from existing nucleic acid sources, including genomic or cDNA, but are preferably produced by synthetic methods. In preferred embodiments each nucleoside unit includes a heterocyclic base and a pentofuranosyl, 2′-deoxypentfuranosyl, trehalose, arabinose, 2′-deoxy-2′-substituted arabinose, 2′-O-substituted arabinose or hexose sugar group. The nucleoside residues can be coupled to each other by any of the numerous known intemucleoside linkages. Such internucleoside linkages include, without limitation, phosphodiester, phosphorothioate, phosphorodithioate, alkylphosphonate, alkylphosphonothioate, phosphotriester, phosphoramidate, siloxane, carbonate, carboalkoxy, acetamidate, carbamate, morpholino, borano, thioether, bridged phosphoramidate, bridged methylene phosphonate, bridged phosphorothioate, and sulfone internucleoside linkages. The term “oligonucleotide” also encompasses polynucleosides having one or more stereospecific internucleoside linkage (e.g., (RP)- or (SP)-phosphorothioate, alkylphosphonate, or phosphotriester linkages). As used herein, the terms “oligonucleotide” and “dinucleotide” are expressly intended to include polynucleosides and dinucleosides having any such internucleoside linkage, whether or not the linkage comprises a phosphate group. In certain preferred embodiments, these internucleoside linkages may be phosphodiester, phosphorothioate, or phosphorodithioate linkages, or combinations thereof.
The term “oligonucleotide” also encompasses polynucleosides having additional substituents including, without limitation, protein groups, lipophilic groups, intercalating agents, diamines, folic acid, cholesterol and adamantane. The term “oligonucleotide” also encompasses any other nucleobase containing polymer, including, without limitation, peptide nucleic acids (PNA), peptide nucleic acids with phosphate groups (PHONA), locked nucleic acids (LNA), morpholino-backbone oligonucleotides, and oligonucleotides having backbone sections with alkyl linkers or amino linkers.
The oligonucleotides of the invention can include naturally occurring nucleosides, modified nucleosides, or mixtures thereof. As used herein, the term “modified nucleoside” is a nucleoside that includes a modified heterocyclic base, a modified sugar moiety, or a combination thereof. In some embodiments, the modified nucleoside is a non-natural pyrimidine or purine nucleoside, as herein described. In some embodiments, the modified nucleoside is a 2′-substituted ribonucleoside an arabinonucleoside or a 2′-deoxy-2′-substituted-arabinoside.
For purposes of the invention, the term “2′-substituted ribonucleoside” or “2′-substituted arabinoside” includes ribonucleosides or arabinonucleosides in which the hydroxyl group at the 2′ position of the pentose moiety is substituted to produce a 2′-substituted or 2′-O-substituted ribonucleoside. Preferably, such substitution is with a lower alkyl group containing 1-6 saturated or unsaturated carbon atoms, or with an aryl group having 6-10 carbon atoms, wherein such alkyl, or aryl group may be unsubstituted or may be substituted, e.g., with halo, hydroxy, trifluoromethyl, cyano, nitro, acyl, acyloxy, alkoxy, carboxyl, carboalkoxy, or amino groups. Examples of 2′-O-substituted ribonucleosides or 2′-O-substituted-arabinosides include, without limitation 2′-O-methylribonucleosides or 2′-O-methylarabinosides and 2′-O-methoxyethoxyribonucleosides or 2′-O-methoxyethoxyarabinosides.
The term “2′-substituted ribonucleoside” or “2′-substituted arabinoside” also includes ribonucleosides or arabinonucleosides in which the 2′-hydroxyl group is replaced with a lower alkyl group containing 1-6 saturated or unsaturated carbon atoms, or with an amino or halo group. Examples of such 2′-substituted ribonucleosides or 2′-substituted arabinosides include, without limitation, 2′-amino, 2′-fluoro, 2′-allyl, and 2′-propargyl ribonucleosides or arabinosides.
The term “oligonucleotide” includes hybrid and chimeric oligonucleotides. A “chimeric oligonucleotide” is an oligonucleotide having more than one type of internucleoside linkage. One preferred example of such a chimeric oligonucleotide is a chimeric oligonucleotide comprising a phosphorothioate, phosphodiester or phosphorodithioate region and non-ionic linkages such as alkylphosphonate or alkylphosphonothioate linkages (see e.g., Pederson et al. U.S. Pat. Nos. 5,635,377 and 5,366,878).
A “hybrid oligonucleotide” is an oligonucleotide having more than one type of nucleoside. One preferred example of such a hybrid oligonucleotide comprises a ribonucleotide or 2′ substituted ribonucleotide region, and a deoxyribonucleotide region (see, e.g., Metelev and Agrawal, U.S. Pat. Nos. 5,652,355, 6,346,614 and 6,143,881).
As used herein, the term “secondary structure” refers to intramolecular and intermolecular hydrogen bonding. Intramolecular hydrogen bonding results in the formation of a stem-loop structure. Intermolecular hydrogen bonding results in the formation of a duplexed nucleic acid molecule.
As used herein, the term “about” implies that the exact number is not critical. Thus, the number of nucleoside residues in the oligonucleotides is not critical, and oligonucleotides having one or two fewer nucleoside residues, or from one to several additional nucleoside residues are contemplated as equivalents of each of the embodiments described above, for purposes of this invention.
As used herein, the term “complementary” means having the ability to hybridize to a nucleic acid. Such hybridization is ordinarily the result of hydrogen bonding between complementary strands, preferably to form Watson-Crick or Hoogsteen base pairs, although other modes of hydrogen bonding, as well as base stacking can also lead to hybridization.
In a second aspect, the invention provides a nucleic acid having reduced immunostimulatory activity. In this aspect the nucleic acid comprises an oligonucleotide sequence containing at least one dinucleotide selected from the group consisting of CpG, C*pG, C*pG* and, CpG*, wherein C is cytidine or 2′-deoxycytidine, G is guanosine or 2′-deoxyguanosine, C* is 2′-deoxythymidine, 1-(2′-deoxy-β-D-ribofuranosyl)-2-oxo-7-deaza-8-methyl-pur ine, 2′-dideoxy-5-nitrocytosine, arabinocytidine, 2′-deoxy-2′-substituted arabinocytidine, 2′-O-substituted arabinocytidine, 2′-deoxy-5-hydroxycytidine, 2′-deoxy-N4-alkyl-cytidine, 2′-deoxy-4-thiouridine, or other pyrimidine nucleoside analogs, G* is 2′-deoxy-7′-deazaguanosine, 2′-deoxy-6-thioguanosine, arabinoguanosine, 2′-deoxy-2′substituted-arabinoguanosine, 2′-O-substituted-arabinoguanosine, 2′-deoxyinosine, or other purine nucleoside analogs, and p is an internucleoside linkage selected from the group consisting of phosphodiester, phosphorothioate, and phosphorodithioate and wherein the oligonucleotide sequence has a secondary structure at the 5′-end of the oligonucleotide sequence. In certain preferred embodiments, the immunostimulatory dinucleotide is not CpG.
In some embodiments, the immunostimulatory nucleic acid is an oligonucleotide sequence from about 2 to about 50 nucleotides in length. In certain embodiments the immunostimulatory nucleic acid is an oligonucleotide sequence from about 12 to about 26 nucleotides in length. In some embodiments, the oligonucleotides each have from about 3 to about 35 nucleoside residues, preferably from about 4 to about 30 nucleoside residues, more preferably from about 4 to about 20 nucleoside residues. In some embodiments, the oligonucleotides have from about 5 to about 18, or from about 5 to about 14, nucleoside residues. As used herein, the term “about” implies that the exact number is not critical. Thus, the number of nucleoside residues in the oligonucleotides is not critical, and oligonucleotides having one or two fewer nucleoside residues, or from one to several additional nucleoside residues are contemplated as equivalents of each of the embodiments described above. In some embodiments, one or more of the oligonucleotides have 11 nucleotides.
In certain embodiments the nucleic acid having reduced immunostimulatory activity forms a 5′-end stem loop secondary structure. In some embodiments, the nucleic acid having reduced immunostimulatory activity has a secondary structure at the 5′-end by way of hydrogen bonding with a complementary sequence. In certain embodiments the nucleic acid having reduced immunostimulatory activity is selected from the group consisting of SEQ ID NOS: 5, 6, 7, 10, 15, 16 and 17.
In a third aspect the invention provides an immunostimulatory nucleic acid comprising at least two oligonucleotides, wherein the immunostimulatory nucleic acid has a secondary structure. In this aspect, immunostimulatory nucleic acid comprises a structure as detailed in formula (I).
Domain A-Domain B-Domain C (I)
Domains may be from about 2 to about 12 nucleotides in length. Domain A may be 5′-3′ or 3′-5′ or 2′-5′ DNA, RNA, RNA-DNA, DNA-RNA having or not having a palindromic or self-complementary domain containing or not containing at least one dinucleotide selected from the group consisting of CpG, C*pG, C*pG* and CpG*, wherein C is cytidine or 2′-deoxycytidine, G is guanosine or 2′-deoxyguanosine, C* is 2′-deoxythymidine, 1-(2′-deoxy-β-D-ribofuranosyl)-2-oxo-7-deaza-8-methyl-pur ine, 2′-dideoxy-5-halocytosine, 2′ dideoxy-5-nitrocytosine, arabinocytidine, 2′-deoxy-2′-substitutedarabinocytidine, 2′-O-substituted arabinocytidine, 2′-deoxy-5-hydroxycytidine, 2′-deoxy-N4-alkyl-cytidine, 2′-deoxy-4-thiouridine, or other pyrimidine nucleoside analogs, G* is 2′ deoxy-7-deazaguanosine, 2′-deoxy-6-thioguanosine, arabinoguanosine, 2′-deoxy-2′substituted-arabinoguanosine, 2′-O-substituted-arabinoguanosine, 2′-deoxyinosine, or other purine nucleoside analogs, and p is an internucleoside linkage selected from the group consisting of phosphodiester, phosphorothioate, and phosphorodithioate. In certain preferred embodiments, the immunostimulatory dinucleotide is not CpG.
In certain embodiments, Domain A will have more than one dinucleotide selected from the group consisting of CpG, C*pG, C*pG* and CpG*.
Domain B, as depicted by an “X” below, is a linker joining Domains A and C that may be a 3′-‘5’ linkage, a 2′-5′ linkage, a 3′-3′ linkage, a phosphate group, a nucleoside, or a non-nucleoside linker that may be aliphatic, aromatic, aryl, cyclic, chiral, achiral, a peptide, a carbohydrate, a lipid, a fatty acid, mono- tri- or hexapolyethylene glycol, or a heterocyclic moiety.
Domain C may be 5′-3′ or 3′-5′, 2′-5′ DNA, RNA, RNA-DNA, DNA-RNA Poly I-Poly C having or not having a palindromic or self-complementary sequence, which can or cannot have a dinucleotide selected from the group consisting of CpG, C*pG, C*pG*, CpG*, wherein C is cytidine or 2′-deoxycytidine, G is guanosine or 2′-deoxyguanosine, C* is 2′-deoxythymidine, 1-(2′-deoxy-β-D-ribofuranosyl)-2-oxo-7-deaza-8-methyl-pur ine, 2′ dideoxy-5-halocytosine, 2′ dideoxy-5-halocytosine, arabinocytidine, 2′-deoxy-2′-substituted arabinocytidine, 2′-O-substituted arabinocytidine, 2′-deoxy-5-hydroxycytidine, 2′-deoxy-N4-alkyl-cytidine, 2′-deoxy-4-thiouridine, other pyrimidine nucleoside analogs, G* is 2′ deoxy-7-deazaguanosine, 2′-deoxy-6-thioguanosine, arabinoguanosine, 2′-deoxy-2′substituted-arabinoguanosine, 2′-O-substituted-arabinoguanosine, 2′-deoxyinosine, or other purine nucleoside analogs, and p is an internucleoside linkage selected from the group consisting of phosphodiester, phosphorothioate, and phosphorodithioate. In certain preferred embodiments, the immunostimulatory dinucleotide is not CpG. In some embodiments, Domain B is preferably a non-nucloetidic linker connecting oligonucleotides of Domain A and Domain C, which are referred to as “immunomers.” In certain preferred embodiments, Domain C does not have the dinucleotide CpG, C*pG, C*pG* or CpG*.
In some embodiments, the oligonucleotides of contained in formula (I) are from about 2 to about 50 nucleotides in length. In certain embodiments the oligonucleotides of contained in formula (I) are from about 12 to about 26 nucleotides in length. In some embodiments, the oligonucleotides each have from about 3 to about 35 nucleoside residues, preferably from about 4 to about 30 nucleoside residues, more preferably from about 4 to about 20 nucleoside residues. In some embodiments, the oligonucleotides have from about 5 to about 18, or from about 5 to about 14, nucleoside residues. As used herein, the term “about” implies that the exact number is not critical. Thus, the number of nucleoside residues in the oligonucleotides is not critical, and oligonucleotides having one or two fewer nucleoside residues, or from one to several additional nucleoside residues are contemplated as equivalents of each of the embodiments described above. In some embodiments, one or more of the oligonucleotides have 11 nucleotides.
By way of non-limiting example, in certain embodiments of this aspect the immunostimulatory nucleic acid will have a structure as detailed in formula (II).
As one skilled in the art would recognize, there is a secondary structure element in the 3′ end of the molecule in the form of an intramolecular stem-loop.
By way of non-limiting example, in certain embodiments of this aspect the immunostimulatory nucleic acid will have a structure as detailed in formula (III)
The structure depicted in formula (III) is referred to herein as a “terminal dimmer,” since the 3′ ends of the two molecules are blocked because the sequences of the two 3′ ends are complementary allowing for intermolecular hydrogen bonding. In addition, domains A and A′ may or may not be identical, domains B and B′ may or may not be identical and domains C and C′ may or may not be identical.
By way of non-limiting example, in certain embodiments of this aspect the immunostimulatory nucleic acid will have a structure as detailed in formula (IV).
As would be recognized by one skilled in the art, the 3′ end of the depicted molecule has a secondary structure because the complementary sequence of its 3′ end is hydrogen bonded to this region. In certain embodiments, a molecule such as a ligand may be attached to the 3′-end in order to facilitate cellular uptake or improve stability of the molecule.
Non-limiting examples of some nucleic acid molecules of the invention are presented in Table 1.
| TABLE 1 | ||
| SEQ ID | ||
| NO: | Sequence* | Structure |
| 1 | 5′-CTGTCTGACGTTCTCTG-3′ |
|
| 2 | 5′-CTGTCTGACGTTCTCTG-GAA- CAGAG-3′ |
|
| 3 | 5′-CTGTCTGACGTTCTCTG-GAA- CAGAGAACGTC-3′ |
|
| 4 | 5′-CTGTCTGACGTTCTCTG-GAA- CAGAGAACGTCAGACAG-3′ |
|
| 5 | 5′-GACAG-GAA- CTGTCTGACGTTCTCTG-3′ |
|
| 6 | 5′-AACGTCAGACAG-GAA- CTGTCTGACGTTCTCTG-3′ |
|
| 7 | 5′-CAGAGAACGTCAGACAG-GAA- CTGTCTGACGTTCTCTG-3′ |
|
| 8 | 5′-CTATCTGACGTTCTCTGT-3′ |
|
| 9 | 5′-CTATCTGACGTTCTCTG- gtgatcag-3′ |
|
| 10 | 5′-gtgatcac- CTATCTGACGTTCTCTGT-3′ |
|
| 11 | 5′-CTGTCTGTCGTTCTCTG-3′ |
|
| 12 | 5′-CTGTCTGTCGTTCTCTG-GAA- CAGAG-3′ |
|
| 13 | 5′-CTGTCTGTCGTTCTCTG-GAA- CAGAGAACGAC-3′ |
|
| 14 | 5′-CTGTCTGTCGTTCTCTG-GAA- CAGAGAACGACAGACAG-3′ |
|
| 15 | 5′-GACAG-GAA- CTGTCTGTCGTTCTCTG-3′ |
|
| 16 | 5′-AACGACAGACAG-GAA- CTGTCTGACGTTCTCTG-3′ |
|
| 17 | 5′-CAGAGAACGACAGACAG-GAA- CTGTCTGTCGTTCTCTG-3′ |
|
| 18 | 5′-TCGTCGTT-CACCTCT- GAA-AGAGCTC-3′ |
|
| 19 | 5′-TCGTCGTT-GTGAGCTCTGT- GAA-ACAGAGCTCAC-3′ |
|
| 20 | 5′-TCGTCGTT- GCACAGAGCTCTGCCT-GAA- AGCAGAGCTCTGTGC-3′ |
|
| 21 | 5′-TCGTCGTT- GCTGACAGAGCTCTGCTAT-GAA- ATAGCAGAGCTCTGTCAGC-3′ |
|
| 22 | 5′-TCGTCGTT-GTGCTCT- GAA-CTTGCTC-3′ |
|
| 23 | 5′-TCGTCGTT- GTGTGCTCTGT-GAA- CATCAGTCTAC-3′ |
|
| 24 | 5′-TCGTCGTT- gagctct-GAA-agagctc-3′ |
|
| 25 | 5′-TCGTCGTT-gtgagctctgt-GAA- acagagctcac-3′ |
|
| 26 | 5′-TCGTCGTT-GAGCTCT- GAA - AGAGCTC -3′- |
|
| 27 | 5′-TCGTCGTT-GTGAGCTCTGT- GAA - ACAGAGCTCAC -3′ |
|
| 28 | 5′-TC G TC G TT-GAGCTCT- GAA-AGAGCTC-3′ |
|
| 29 | 5′-TC G TC G TT- GAGCTCT-GAA- AGAGCTC-3′ |
|
| 30 | 5′-TGCTGCTT-GAGCTCT- GAA-AGAGCTC-3′ |
|
| 31 | 5′-TCTTGACGTTCTCTCT-3′ |
|
| 32 | 5′-TCTTGACGTTCTCTCT-GAA- AGAGAG-3′ |
|
| 33 | 5′-TCTTGACGTTCTCTCT-GAA- agagag-3′ |
|
| 34 | 5′-tcttgacgttctctct-GAA- AGAGAG-3′ |
|
| 35 | 5′-tcttgacgttctctct-GAA- agagag-3′ |
|
| 36 | 5′-tcttgacgttctctct-gaa- agagag-3′ |
|
| 37 | 5′-TCTTGACGTTCTCTCT-X- AGAGAG-3′ |
|
| 38 | 5′-tcttgacgttctctct-X- agagag-3′ |
|
| *upper case-PS; lower case-PO; Bold-2′-O-methyl-ribonucleotides (in 26 and 27); G-2′-deoxy-7-deaza-G (in 28); G -araG (in 29); X-C3-linker (in 37 and 38). | ||
Alternatively, the nucleic acid molecule of the invention can be two immunomers linked by way of a non-nucleotidic linker. Non-limiting representative examples of these molecules are presented in Table 2.
| TABLE 2 | ||
| SEQ | ||
| ID | ||
| NO: | Sequence* | Structure |
| 39 | 5′-TCGTCGTTX-GTCTCGAGAC-5′ |
|
| 40 | 5′-TCGTCGTTT-XX- GTCTCGAGAC-5′ |
|
| 41 | 5′-TCGTCGTT-XXX- GTCTCGAGAC-5′ |
|
| 42 | 5′-TCGTCGTT-Y-GTCTCGAGAC-5′ |
|
| 43 | 5′-TCGTCGTT-Z-GTCTCGAGAC-5′ |
|
| 44 | 5′-TCGTCGTT-XXX- GUCUCGAGAC -5′ |
|
| 45 | 5′-TC G TC G TT-XXX- GTCTCGAGAC-5′ |
|
| 46 | 5′-TTGTGCTT-XXX- GTCTCGAGAC-5′ |
|
| 47 | 5′-TCGTCGTT-XXX- GTCTCCACAC-5′ |
|
| 48 | 5′-TCGTCGTT-XXX-ccgtagctacGG-5′ |
|
| 49 | 5′-TCGTCGTT-XX-ccgtagctacGG-5′ |
|
| 50 | 5′-TCGTCGTT-X-ccgtagctacGG-5′ |
|
| 51 | 5′-TCGTCGTT-3′-3′-ccgtagctacGG-5′ |
|
| 52 | 5′-TCGTCGTT-Y-ccgtagctacGG-5′ |
|
| 53 | 5′-TCGTCGTT-Z-ccgtagctacGG-5′ |
|
| 54 | 5′-TCGTCGTT-XXX-ctcgag-5′ |
|
| 55 | 5′-TCGTCGTT-XXX-ctgtctcgagacag-5′ |
|
| 56 | 5′-TCGTCGTT-XXX- cgactgtctcgagacagtcg-5′ |
|
| 57 | 5′-TCGTCGTT-XXX- gucucgagac -5′ |
|
| 58 | 5′-TCGTCGTTG-X-tgcatcgatgca-3′-X- 3′-GTTGCTGCT-5′ |
|
| 59 | 5′-TCGTCGTTG-3′-X-3′-tgcatcgatgca- X-GTTGCTGCT-5′ |
|
| 60 | 5′-TCGTCGTTG-X-TGCATCGATGCA- 3′-X-3′-GTTGCTGCT-5′ |
|
| 61 | 5′-TCGTCGTTG-3′-X-3′- TGCATCGATGCA-X- GTTGCTGCT-5′ |
|
| 62 | 5′-tcgtcgttg-X-TGCATCGATGCA- 3′-X-3′-gttgctgct-5′ |
|
| 63 | 5′-tcgtcgttg-3′-X-3′- TGCATCGATGCA-X- gttgctgct-5′ |
|
| 64 | 5′-tcgtcgtt-XXX-gtctcgagac-5′ |
|
| 65 | 5′-TCGTCGTT-XXX-gtctcgagac-5′ |
|
| 66 | 5′-TCGTCGTTG-X-tgcatcgatgca-3′ |
|
| 67 | 5′-TCGTCGTTGtgcatcgatgca-3′ |
|
| 68 | 5′-tcgtcgttgTGCATCGATGCA-3′ |
|
| *Upper case-PS; lower case-PO, X-C3-linker; Y-tetraethyleneglycol linker; Z-hexaethyleneglycol linker, bold-2′-O-methylribonucleotides (in 44 and 57); G-2′-deoxy-7-deaza-G (in 45). | ||
In certain embodiments, the immunostimulatory nucleic acids of the invention have sequence selected from the group consisting of SEQ ID NOS: 1-38. In some embodiments, the immunostimulatory nucleic acids of the invention have a sequence selected from the group consisting of SEQ ID NOS: 39-68.
In certain embodiments of the invention, at least one immunostimulatory oligonucleotide of the invention comprises an immunostimulatory dinucleotide of the formula 5′-Pyr-Pur-3′, wherein Pyr is a natural pyrimidine nucleoside or analog thereof and Pur is a natural purine nucleoside or analog thereof. As used herein, the term “pyrimidine nucleoside” refers to a nucleoside wherein the base component of the nucleoside is a pyrimidine base. Similarly, the term “purine nucleoside” refers to a nucleoside wherein the base component of the nucleoside is a purine base. For purposes of the invention, a “synthetic” pyrimidine or purine nucleoside includes a non-naturally occurring pyrimidine or purine base, a non-naturally occurring sugar moiety, or a combination thereof.
Preferred pyrimidine nucleosides in the immunostimulatory oligonucleotides and/or immunomers used in the method according to the invention have the structure (I):
wherein:
D is a hydrogen bond donor;
D′ is selected from the group consisting of hydrogen, hydrogen bond donor, hydrogen bond acceptor, hydrophilic group, hydrophobic group, electron withdrawing group and electron donating group;
A is a hydrogen bond acceptor or a hydrophilic group;
A′ is selected from the group consisting of hydrogen bond acceptor, hydrophilic group, hydrophobic group, electron withdrawing group and electron donating group;
X is carbon or nitrogen; and
S′ is a pentose or hexose sugar ring, or a non-naturally occurring sugar.
Preferably, the sugar ring is derivatized with a phosphate moiety, modified phosphate moiety, or other linker moiety suitable for linking the pyrimidine nucleoside to another nucleoside or nucleoside analog.
Preferred hydrogen bond donors include, without limitation, —NH—, —NH 2 , —SH and —OH. Preferred hydrogen bond acceptors include, without limitation, C═O, C═S, and the ring nitrogen atoms of an aromatic heterocycle, e.g., N3 of cytosine.
In some embodiments, the base moiety in (I) is a non-naturally occurring pyrimidine base. Examples of preferred non-naturally occurring pyrimidine bases include, without limitation, 5-hydroxycytosine, 5-hydroxymethylcytosine, N4-alkylcytosine, preferably N4-ethylcytosine, and 4-thiouracil. In some embodiments, the sugar moiety S′ in (I) is a non-naturally occurring sugar moiety. For purposes of the present invention, a “naturally occurring sugar moiety” is a sugar moiety that occurs naturally as part of nucleic acid, e.g., ribose and 2′-deoxyribose, and a “non-naturally occurring sugar moiety” is any sugar that does not occur naturally as part of a nucleic acid, but which can be used in the backbone for an oligonucleotide, e.g, hexose. Arabinose and arabinose derivatives are examples of preferred sugar moieties.
Preferred purine nucleoside analogs in immunostimulatory oligonucleotides and/or immunomers used in the method according to the invention have the structure (II):
wherein:
D is a hydrogen bond donor;
D′ is selected from the group consisting of hydrogen, hydrogen bond donor, and hydrophilic group;
A is a hydrogen bond acceptor or a hydrophilic group;
X is carbon or nitrogen;
each L is independently selected from the group consisting of C, O, N and S; and
S′ is a pentose or hexose sugar ring, or a non-naturally occurring sugar.
Preferably, the sugar ring is derivatized with a phosphate moiety, modified phosphate moiety, or other linker moiety suitable for linking the pyrimidine nucleoside to another nucleoside or nucleoside analog.
Preferred hydrogen bond donors include, without limitation, —NH—, —NH 2 , —SH and —OH. Preferred hydrogen bond acceptors include, without limitation, C═O, C═S, —NO 2 and the ring nitrogen atoms of an aromatic heterocycle, e.g., N1 of guanine.
In some embodiments, the base moiety in (VI) is a non-naturally occurring purine base. Examples of preferred non-naturally occurring purine bases include, without limitation, 6-thioguanine and 7-deazaguanine. In some embodiments, the sugar moiety S′ in (II) is a naturally occurring sugar moiety, as described above for structure (I).
In a fourth aspect, the invention provides a method for reducing or eliminating the immunostimulatory activity of an oligonucleotide. The method comprises introducing at the 5′-end of a CpG-containing oligonucleotide a nucleic acid sequence comprising a secondary structure. In some embodiments of this aspect, the secondary structure is a stem-loop structure. In certain embodiments of this aspect, the secondary structure is obtained by hydrogen bonding a complementary sequence to the 5′-end of the oligonucleotide sequence.
In a fifth aspect, the invention provides a method for increasing the stability of an immunostimulatory oligonucleotide. The method comprises introducing at the 3′-end of the immunostimulatory oligonucleotide a nucleic acid sequence comprising a secondary structure. In some embodiments of this aspect, the secondary structure is a stem-loop structure. In certain embodiments of this aspect, the secondary structure is obtained by hydrogen bonding a complementary sequence to the 3′-end of the oligonucleotide sequence.
In a sixth aspect, the invention provides a method for modulating the immunostimulatory activity of an immunostimulatory oligonucleotide. The method comprises introducing at the 3′-end or the 5′-end of the immunostimulatory oligonucleotide a nucleic acid sequence comprising a secondary structure. In some embodiments of this aspect, the secondary structure is a stem-loop structure. In certain embodiments of this aspect, the secondary structure is obtained by hydrogen bonding a complementary sequence to the 3′-end or 5′-end of the oligonucleotide sequence.
As used herein, the term “modulating” or “modulate” means to increase or decrease the immunostimulatory activity of an immunostimulatory nucleic acid relative to that of the parent immunostimulatory nucleic acid.
In a seventh aspect the invention provides pharmaceutical compositions. These compositions comprise any one of the compositions disclosed in the first, second and third aspects of the invention either alone or in combination and a pharmaceutically acceptable carrier.
As used herein, the term “physiologically acceptable” refers to a material that does not interfere with the effectiveness of the compositions of the first, second or third aspects of the invention and is compatible with a biological system such as a cell, cell culture, tissue, or organism. Preferably, the biological system is a living organism, such as a vertebrate.
As used herein, the term “carrier” encompasses any excipient, diluent, filler, salt, buffer, stabilizer, solubilizer, lipid, or other material well known in the art for use in pharmaceutical formulations. It will be understood that the characteristics of the carrier, excipient, or diluent will depend on the route of administration for a particular application. The preparation of pharmaceutically acceptable formulations containing these materials is described in, e.g., Remington's Pharmaceutical Sciences, 18th Edition, ed. A. Gennaro, Mack Publishing Co., Easton, Pa., 1990, ISBN: 0-912734-04-3.
Pharmaceutical compositions of the invention may also include a cancer vaccine, including a cancer vaccine selected from the group consisting of EFG, Anti-idiotypic cancer vaccines, Gp75 antigen, GMK melanoma vaccine, MGV ganglioside conjugate vaccine, Her2/new, Ovarex, M-Vax, O-Vax, L-Vax, STn-KHL theratope, BLP25 (MUC-1), liposomal idiotypic vaccine, Melacine, peptide antigen vaccines, toxin/antigen vaccines, MVA-vased vaccine, PACIS, BCG vaccine, TA-HPV, TA-CIN, DISC-virus and ImmunCyst/TheraCys.
In various embodiments of the invention, the compositions of the first, second, third, fourth, fifth or sixth aspects of the invention may be covalently linked to an antigen or otherwise operatively associated with an antigen. As used herein, the term “operatively associated with” refers to any association that maintains the activity of both the compositions of the first, second or third aspects of the invention and the antigen. Non-limiting examples of such operative associations include being part of the same liposome or other such delivery vehicle or reagent. In embodiments wherein the compositions of the first, second or third aspects of the invention are covalently linked to an antigen, such covalent linkage preferably is at any position on the compositions of the first, second or third aspects of the invention other than an accessible 5′ end of an immunostimulatory oligonucleotide. For example, the antigen may be attached at an internucleoside linkage or may be attached to the non-nucleotidic linker. Alternatively, the antigen may itself be the non-nucleotidic linker.
In various embodiments of the invention, the compositions of the first, second, third, fourth, fifth or sixth aspects of the invention may include an oligonucleotide with antisense activity. As used herein, “antisense activity” means that the oligonucleotide, when introduced into a cell or an animal, causes a reduction in the expression of the gene to which it is complementary.
In various embodiments of the invention, the compositions of the first, second, third, fourth, fifth or sixth aspects of the invention may include an oligonucleotide sequence that is an aptamer. Aptamers are nucleic acid molecules that have been selected from random pools based on their ability to bind other molecules. Aptamers have been selected which bind nucleic acids, proteins, small organic compounds, and even entire organisms. These novel molecules have many potential uses in medicine and technology (see, e.g., Burgstaller P., et al. Curr Opin Drug Discov Devel. 5: 690-700 (2002)).
The pharmaceutical compositions of the invention may be administered by any suitable route, including, without limitation, parenteral, oral, sublingual, transdermal, topical, intranasal, aerosol, intraocular, intratracheal, intrarectal, vaginal, by gene gun, dermal patch or in eye drop or mouthwash form. The pharmaceutical compositions can be delivered using known procedures at dosages and for periods of time effective obtain the desired effect, e.g. the treatment of cancer, the treatment of infection and the treatment of autoimmune diseases. When administered systemically, the pharmaceutical compositions are preferably administered at a sufficient dosage to attain a blood level of the compositions of the first, second and/or third aspects of the invention from about 0.0001 micromolar to about 10 micromolar. For localized administration, much lower concentrations than this may be effective, and much higher concentrations may be tolerated. Preferably, a total dosage of immunostimulatory oligonucleotide and/or immunomer ranges from about 0.0001 mg per patient per day to about 200 mg per kg body weight per day. It may be desirable to administer simultaneously, or sequentially a therapeutically effective amount of one or more of the therapeutic compositions of the invention to an individual as a single treatment episode.
In addition, when immunostimulatory oligonucleotides were created as immunomers the following protocols were used for synthesis. The immunostimulatory oligonucleotides and/or immunomers of the invention may conveniently be synthesized using an automated synthesizer and phosphoramidite approach as schematically depicted in FIGS. 9 and 11. In some embodiments, the immunostimulatory oligonucleotides and/or immunomers are synthesized by a linear synthesis approach (see FIG. 9). Representative linkers for this synthesis are presented in FIG. 10. As used herein, the term “linear synthesis” refers to a synthesis that starts at one end of the immunomer and progresses linearly to the other end. Linear synthesis permits incorporation of either identical or un-identical (in terms of length, base composition and/or chemical modifications incorporated) monomeric units into the immunostimulatory oligonucleotides and/or immunomers.
An alternative mode of synthesis for immunomers is “parallel synthesis”, in which synthesis proceeds outward from a central linker moiety (see FIG. 11). Representative linkers for this method of synthesis are presented in FIG. 12. A solid support attached linker can be used for parallel synthesis, as is described in U.S. Pat. No. 5,912,332. Alternatively, a universal solid support, such as phosphate attached to controlled pore glass support, can be used.
Parallel synthesis of immunomers has several advantages over linear synthesis: (1) parallel synthesis permits the incorporation of identical monomeric units; (2) unlike in linear synthesis, both (or all) the monomeric units are synthesized at the same time, thereby the number of synthetic steps and the time required for the synthesis is the same as that of a monomeric unit; and (3) the reduction in synthetic steps improves purity and yield of the final immunomer product.
At the end of the synthesis by either linear synthesis or parallel synthesis protocols, the immunostimulatory oligonucleotides or immunomers according to the invention may conveniently be deprotected with concentrated ammonia solution or as recommended by the phosphoramidite supplier, if a modified nucleoside is incorporated. The product immunostimulatory oligonucleotides and/or immunomer is preferably purified by reversed phase HPLC, detritylated, desalted and dialyzed.
The stimulatory domain of CpG DNAs 18-21 contained a human specific ′GTCGTT′ motif at the 5′-end. In the structural domain region, complementary sequences that formed 7, 11, 15, or 19 base-pair (bp) hairpin stem-loop structures were incorporated adjacent to the 3′-end of the stimulatory domain (Table 3). Self-stabilized CpG DNAs were designed such that the stimulatory domain did not contain any structural motifs (base-pairing) and CpG stimulatory motifs were not present in the structural domain. Both a stimulatory motif and a secondary structure in CpG DNAs are required for pDC activation. CpG DNAs induced strong concentration-dependent proliferation of human B cells in culture. However, B-cell proliferation was not dependent on the length of the hairpin duplex. The ability of self-stabilized CpG DNAs to activate both pDCs and B cells may permit the development of therapeutic agents for use against cancer, asthma, allergy, and infectious diseases and as adjuvant more potent than those that stimulate either B cells or pDCs.
Sequence 22 had a stimulatory domain but did not contain the required complementarity to form a hairpin structure at its 3′-end (structural domain). On the contrary, CpG DNA 30 formed a hairpin structure (structural domain) but did not have a stimulatory motif (Table 3). Sequence 69, an analog of sequence 19, contained 2′-O-methyl-ribonucleotides in one of the strands of the hairpin sequence.
The formation of stable hairpin structures by CpG DNAs was confirmed by thermal melting (Table 3) and EMSA studies. As expected CpG DNAs 18-21 showed bands with required mobility on a non-denaturing polyacrlyamide gel compared with oligonucleotide markers of different lengths and structures confirmed hairpin structure formation (data not shown).
Human pDCs express TLR9 and are believed to be the main source of CpG DNA-induced IFN-α. CpG DNAs 18-21 induced the production of IFN-α in human pDC cultures as shown in FIG. 13. The levels of IFN-α secretion depended on the length of the hairpin duplex structure. CpG DNA 21, which formed a 19-bp duplex, induced the highest levels of IFN-α (FIG. 13). While the response varied from donor to donor, the trend was consistent among the CpG DNAs (FIG. 13). CpG DNA 70, a palindromic CpG oligo containing poly(dg) sequences and known to stimulate human pDCs, was used as a positive control.
All four CpG DNAs induced strong concentration-dependent proliferation of human B cells in culture (FIG. 14). However, B-cell proliferation was not dependent on the length of the hairpin duplex (FIG. 13).
Activation of human pDCs to induce IFN-α secretion by CpG DNAs 18, 19, 22, and 30 was studied. As seen in previous experiments, both 18 and 19 induced production of IFN-α (FIG. 15). Sequences 22, with a stimulatory motif but no secondary structure, and 30, with no stimulatory motif but with a secondary structure, failed to induce IFN-α production in pDC cultures (FIG. 15). These results suggest that both a stimulatory motif and a secondary structure in CpG DNAs were required for pDC activation.
The data for B-cell proliferation presented in FIG. 4B show that CpG DNAs 18 and 19, which formed secondary structures, and 22, which did not, induced strong B-cell proliferation. Sequence 30, which did not have a stimulatory motif, induced minimal proliferation, suggesting that a CpG motif was required for activity but a secondary structure was not.
TLR9 specifically recognizes CpG DNA but not RNA. However, site-specific incorporation of 2′-O-alkylribonucleotides distal to the CpG dinucleotide in the flanking sequences is tolerated. We synthesized an analog of CpG DNA 19, in which the stem sequence close to the 3′-end, including the loop region, was replaced with 2′-O-methylribonucleotides. Both CpG DNAs 69 and 19 induced similar levels of IFN-α secretion in human pDC cultures (FIG. 16) and proliferation in human B-cell cultures (FIG. 16). These results suggested that 2′-O-methylribonucleotide substitutions or the conformational changes imposed by these substitutions did not interfere with either pDC or B-cell activation.
Toll-like receptor 9 (TLR9) recognizes unmethylated CpG DNA and activates several signaling pathways, including stress-kinase and NF-κB pathways, leading to the secretion of a number of chemokines and cytokines including IFN-α/β, IFN-γ, IL-12, IL-6, and TNF-α in vitro and in vivo. However, a direct interaction between CpG DNA and its receptor, TLR9, has not been established yet. The possible role of alternate receptors or co-receptors in CpG DNA immune stimulation has been proposed. CpG DNAs with different backbones, sequences, and structures activate the immune system in a cell-specific but TLR9-dependent fashion.
Optimal placement of a secondary structure at the 3′-end of CpG DNA could induce different cytokine profiles. CpG DNA structures with a human-specific motif induced high levels of IFN-α in human pDC cultures, suggesting that secondary structures may be required for pDC activation (unpublished data).
The present CpG DNAs were designed to contain two distinct domains, a stimulatory domain with a CpG-motif at the 5′-end and a structural domain containing sequences that permitted hairpin duplex formation at the 3′-end. The ability of these CpG DNAs to form intramolecular secondary structures provided additional stability against ubiquitous 3′-nucleases, hence the name self-stabilized CpG DNAs. Self-stabilized CpG DNAs differ from earlier reported palindromic CpG DNAs, which form intermolecular secondary structures and by not having CpG motifs in the structural domain region.
Palindromic sequences containing a CpG dinucleotide activate immune cells to produce IFN-α/β and -γ. The self-stabilized CpG DNAs described here allowed us to dissect the stimulatory and structural features of CpG DNA that were recognized by both human B cells and pDCs. CpG DNAs 18-21 activated pDCs in a hairpin duplex length-dependent fashion. Both control DNA molecules 22, with no structural domain, and 30, with no stimulatory domain, failed to induce IFN-α secretion, suggesting that both stimulatory and structural domains were required for pDC activation. On the contrary, B-cell activation required only the stimulatory domain and not the structural domain. The lower activity of CpG DNAs 20 and 21 suggested that secondary structures in CpG DNA may have interfered with B-cell activation. In fact, CpG DNA 30, which had no structural domain and was equal in nucleotide length to CpG DNA 18, activated B cells to a level equal to that of 19, suggesting that single-stranded DNAs were preferred for B-cell activation. The lower activation of B cells observed with 30 could be related to non-specific activity.
The present results with CpG DNA 69 suggested that the DNA/RNA hybrid heteroduplex did not impede either pDC or B cell activation. These results suggested that the B to A conformational changes imposed by the 2′-O-methylribonucleotide substitutions with in the structural domain region had little or no influence on immune stimulation, thus allowing substitutions at these positions
In conclusion, in these studies we proposed a rational combination of stimulatory and structural domains in CpG DNAs for optimal activation of TLR9-positive subsets of human immune cells, pDCs and B cells. The studies presented here allowed us to determine the specific characteristics of CpG DNAs required for activation of pDCs and B cells. A CpG stimulatory motif was required for the activation of human B cells, while both the stimulatory motif and an additional structural domain were required for the activation of human pDCs. It is unclear why the same TLR9 receptor required different structural characteristics of its ligands for stimulation in two different cell populations. The fact that it did could indicate the involvement of different adapter molecules in TLR9 signaling in pDCs and B cells. The ability of self-stabilized CpG DNAs to activate both pDCs and B cells will permit the development of therapeutic agents for use against cancer, asthma, allergy, and infectious diseases and as adjuvant more potent than those that stimulate either B cells or pDCs.
| TABLE 3 | ||
| Schematic drawing a , sequences, secondary structures and | ||
| T m s of CpG DNAs | ||
|
| ||
| SEQ | ||
| ID | ||
| NO | Sequence (5′---->3′) b | T m , ° C. |
| 18 | TCGTCGTT-GAGCTCT G A | 45.2 |
| CTCGAGA A | ||
| 19 | TCGTCGTT-GTGAGCTCTGT G A | 53.0 |
| CACTCGAGACA A | ||
| 20 | TCGTCGTT-GCACAGAGCTCTGCT G A | 68.7 |
| CGTGTCTCGAGACGA A | ||
| 21 | TCGTCGTT- | 72.8 |
| GCTGACAGAGCTCTGCTAT G A | ||
| CGACTGTCTCGAGACGAT A | ||
| 22 | TCGTCGTT-GTGCTCT-GAA-CTTGCTC | <8.0 |
| 30 | TGCTGCTT-GAGCTCT G A | 44.1 |
| CTCGAGA A | ||
| 69 | TCGTCGTT-GTGAGCTCTGT A A | 66.5 |
| CACUCGAGACA A | ||
| 70 | GGTGCATCGATGCAGGGGGG | ND c |
| GGGGGGACGTAGCTACGTGG | ||
| a Schematic drawing of the novel CpG DNA design (box) showing the essential stimulatory and structural domains. The stimulatory domain, but not the structural domain, contained an appropriate CpG motif; | ||
| b All sequences are phosphorothioate modified except 70 Nucleotides shown in italic 69 indicate 2′-O-methylribonucleotides, underlined nucleotides in 70 indicate phosphodiester backbone; | ||
| c ND-not determined. | ||
The examples below are intended to further illustrate certain preferred embodiments of the invention, and are not intended to limit the scope of the invention.
EXAMPLES
Example 1
Oligonucleotide Synthesis, Purification and Thermal Melt Profiles
CpG oligos were synthesized on a 1 to 2 pmole scale using β-cyanoethylphosphoramidites on a PerSeptive Biosystem's 8909 Expedite DNA synthesizer (PerSeptive Biosystem, Boston, Mass.). The phosphoramidites of dA, dG, dC, and T were obtained from PE Biosystems (Foster City, Calif.). As described by Iyer R. P., et al. ( J. Am. Chem. Soc. 112: 1253-1254 (1990)), an iodine oxidizing agent was used to obtain the phosphorothioate backbone modification. All oligos were deprotected using standard protocols, purified by HPLC, and dialyzed against USP quality sterile water for irrigation. The oligos were lyophilized and dissolved again in distilled water and the concentrations were determined from UV absorbance at 260 nm. All oligos were characterized by CGE and MALDI-TOF mass spectrometry (Applied Biosystem's Voyager-DETM STR Biospectrometry™ Workstation) for purity and molecular mass, respectively. The purity of full-length oligos ranged from 90-96% with the rest being shorter by one or two nucleotides (n-1 and n-2) as determined by CGE and/or denaturing PAGE. All oligos contained less than <0.1 EU/mL of endotoxin as determined by the Limulus assay (Bio-Whittaker now known as Cambrex Bio Science Walkersville, Inc., Walkersville, Md.).
Thermal melting studies were carried out in 1 mL solution of 10 mM disodium hydrogen phosphate, pH 7.2±0.2, containing 150 mM NaCl, and 2 mM MgCl2. The solutions were heated to 95° C. for 10 min and allowed to come to room temperature slowly before being stored at 4° C. overnight. The final concentration of oligonucleotide strand was 2.0 μM. UV thermal melting measurements were performed at 260 nm on a Perkin-Elmer Lambda 20 Spectrophotometer attached to a peltier thermal controller and a personal computer using 1 cm path length quartz cuvettes at a heating rate of 0.5° C./min. Melting temperatures (Tm) were taken as the temperature of half-dissociation and were obtained from first derivative plots. Each Tm value is an average of two or three independent experiments and the values were within ±1.0° C.
A 17-mer phosphorothioate oligonucleotide (1) containing a ‘GACGTT’ hexameric motif was used as a positive control (Table 1). Oligonucleotides 2-7 contain additional sequences of five-, eleven, or seventeen nucleotides complementary to parts of 1 (Table 1). Extensions are linked either at the 3′-(2-4) or 5′-end (5-7) and contain a GAA trimer that allows formation of a stable stem-loop as described by Hirao, I., et al. ( Nucleic Acids Res. 22: 576-582 (1994)). Formation of hairpins by 2-7 was determined by UV thermal melting experiments. The Tm values of 40-66° C. in 10 mM sodium phosphate, pH 7.2, containing 150 mM NaCl, and 2 mM MgCl2 suggests that 2-7 formed stable secondary structures under the experimental conditions (Table 1). of interferon α (IFN-α) in plasmacytoid dendritic cells after exposure to oligos 18, 19, 20, and 21 at 10 μg/ml.
Example 2
Cell Culture Conditions and Reagents
Spleen cells from 4-8 week old BALB/c, C57BL/6 or C3H/HeJ mice were cultured in RPMI complete medium as described by Zhao, Q., et al. ( Biochem Pharmacol. 51: 173-182 (1996)) and Branda, R. F., et al. ( Biochem. Pharmacol. 45: 2037-2043 (1993)). Murine J774 macrophages (American Type Culture Collection, Manassas, Va.) were cultured in Dulbecco's modified Eagles medium supplemented with 10% (v/v) fetal calf serum and antibiotics (100 IU/mL of penicillin G/streptomycin). All other culture reagents were purchased from Mediatech (Gaithersburg, Md.).
Example 3
Spleen Cell Proliferation Assay
Typically, mouse (Balb-C) spleen cells were cultured with CpG oligos at concentrations of 0.1, 1.0, and 10.0 μg/ml for 48 h and cell proliferation was determined by 3H-uridine incorporation, as described by Zhao, Q., et al. ( Biochem Pharmacol. 51: 173-182 (1996)).
Initially, oligos 1, 2, and 5 were examined for their ability to induce proliferation of BALB/c mouse spleen cells in cultures. Oligos 1 and 2 induced a dose-dependent spleen cell proliferation. The parent oligo 1, which did not have a stem-loop structure, showed a proliferation index of 6.0±0.3 at a concentration of 1.0 μg/mL (FIG. 1A). Oligo 2, which forms a stem-loop structure at its 3′-end gave a proliferation index of 9.0±2.5 at the same concentration. Oligo 5, which forms a stem-loop at its 5′-end, however, showed a lower proliferation index of 1.5±0.3 at the same concentration, which is similar to that of PBS control (FIG. 1A).
Example 4
Cytokine Induction Assays
Mouse spleen or J774 cells were plated in 24-well dishes using 5×10 6 or 1×10 6 cells/mL, respectively. The CpG oligos dissolved in TE buffer (10 mM Tris-HCl, pH 7.5, 1 mM EDTA) were added to a final concentration of 0.03, 0.1, 0.3, 1.0, 3.0, or 10.0 μg/mL to the cell cultures. The cells were then incubated at 37° C. for 24 hr and the supernatants were collected for ELISA assays. The experiments were performed two or three times for each CpG oligo and in triplicate for each concentration. The secretion of IL-12 and IL-6 was measured by sandwich ELISA as described by Bhagat L., et al. ( Biochem. Biophys. Res. Commun. 300: 853-861 (2003)). The required reagents, including cytokine antibodies and standards were purchased from BD Biosciences Pharmingen (San Diego, Calif.).
CpG oligos induce a number of cytokines including IL-12 and IL-6. In BALB/c mouse spleen cell cultures test compounds 1 and 2 induced IL-12 and IL-6 by a concentration-dependent mechanism. Parent oligo 1 induced 1514±113 pg/mL of IL-12 and 7681±839 pg/mL of IL-6 at 3.0 μg/mL concentration (FIG. 2). Olig