Chimeric antigens for eliciting an immune response
View Patent ↗Disclosed herein are the nucleotide sequences, deduced amino acid sequences as well as methods and compositions necessary to elicit immune responses against chronic Hepatitis B infections in animals and humans. Immune response is enhanced by fusing relevant viral antigens with xenotypic immunoglobulin heavy chain region through a peptide linker and producing the fusion proteins in Baculovirus expression system to incorporate high mannose glycosylation. By virtue of the antibody component, the fusion proteins bind to Fc receptors on the surface of antigen presenting cells, are taken up, processed and derived peptides are presented on MHC Class I, which elicit a CTL (Th1) response. In a similar fashion, due to cross priming and presentation on MHC Class II, will elicit a humoral (Th2) response. In addition, disclosed are the methods of cloning, expression and production of the fusion proteins.
1. A composition for eliciting a T-cell response in vivo, the composition comprising a purified chimeric fusion protein antigen, the chimeric fusion protein antigen comprising an immune response domain and a target binding domain expressed from an open reading frame encoding the immune response domain and the target binding domain fused together genetically,
wherein the immune response domain comprises one or more HBV surface antigens, or antigenic epitopes thereof, and
wherein the target binding domain consists of an Ig hinge region, at least a portion of a C H 1 region and a xenotypic Fc antibody fragment comprising at least part of a C H 2 and C H 3 domain; and
wherein the chimeric fusion protein antigen comprises non-mammalian glycosylation.
2. The composition of claim 1 , wherein the one or more HBV surface antigens are selected from the group consisting of one or more of HBV S polypeptide, HBV S1 polypeptide, and HBV S2 polypeptide.
3. The composition of claim 1 , wherein a His tag is linked to the chimeric antigen.
4. The composition of claim 1 , wherein the target binding domain is capable of binding to an antigen presenting cell.
5. The composition of claim 4 , wherein the antigen presenting cell is a dendritic cell.
6. The composition of claim 1 , wherein the antibody fragment is a murine antibody fragment.
7. The composition of claim 1 , wherein the immune response domain comprises one or more antigenic sequences.
8. The composition of claim 1 , wherein the composition has the ability to induce (a) a T H 1 immune response, (b) a T H 2 immune response, or (c) a T H 1 immune response and a T H 2 immune response.
9. The composition of claim 1 , wherein the immune response domain is linked to a 6-His tag and a recombinant tobacco etch virus (rTEV) protease cleavage site.
10. The composition of claim 1 , wherein the one or more HBV surface antigens comprises HBV S1/S2 protein.
11. The composition of claim 1 , wherein the one or more HBV surface antigens are selected from the group consisting of HBV S1/S2/S protein and HBV S2/S protein.
12. The composition of claim 1 , wherein the glycosylation comprises mannose glycosylation.
13. The composition of claim 1 , further comprising a cell.
14. The composition of claim 13 , wherein the cell is an antigen presenting cell.
15. The composition of claim 13 , wherein the cell is a cultured cell.
16. The composition of claim 1 , wherein the composition comprises a monomer comprising an immune response domain and a target binding domain.
17. The composition of claim 16 , wherein the composition comprises a dimer of the monomer.
18. The composition of claim 3 , wherein the His tag is a 6 His peptide.
19. The composition of claim 3 , wherein the His tag is linked to immune response domain.
20. The composition of claim 3 , wherein the His tag is linked to the target binding domain.
21. A composition for eliciting a T-cell response in vivo, the composition comprising a purified chimeric fusion protein antigen, the chimeric fusion protein antigen comprising an immune response domain and a target binding domain expressed from an open reading frame encoding the immune response domain and the target binding domain fused together genetically,
wherein the target binding domain consists of an Ig hinge region, at least a portion of a C H 1 region and a xenotypic Fc antibody fragment comprising at least part of a C H 2 and C H 3 domain;
wherein the Fc antibody fragment is capable of binding to an Ig Fc receptor or an antigen presenting cell; and
wherein the chimeric fusion protein antigen comprises non-mammalian glycosylation.
22. The composition of claim 21 , wherein the immune response domain comprises one or more HBV antigens, or antigenic epitopes thereof.
23. The composition of claim 22 , wherein the one or more HBV antigens are HBV antigens comprising one or more HBV surface antigens.
24. The composition of claim 23 , wherein the one or more HBV surface antigens are selected from the group consisting of one or more of HBV S protein, HBV S1 protein, and HBV S2 protein.
25. The composition of claim 24 , wherein the one or more HBV surface antigens comprise HBV S1/S2 protein.
26. The composition of claim 24 , wherein the one or more HBV surface antigens are selected from the group consisting of HBV S1/S2/S protein and HBV S2/S protein.
27. The composition of claim 21 , wherein a 6-His-peptide is linked to the immune response domain.
28. The composition of claim 21 , wherein the target binding domain is capable of binding to an antigen presenting cell.
29. The composition of claim 28 , wherein the antigen presenting cell is a dendritic cell.
30. The composition of claim 21 , wherein the immune response domain comprises one or more antigenic sequences.
31. The composition of claim 21 , wherein the composition has the ability to induce (a) a T H 1 immune response, (b) a T H 2 immune response, or (c) a T H 1 immune response and a T H 2 immune response.
32. The composition of claim 21 , wherein the glycosylation comprises mannose glycosylation.
33. The composition of claim 21 , wherein the immune response domain is linked to a 6-His tag and a recombinant tobacco etch virus (rTEV) protease cleavage site.
34. The composition of claim 21 , further comprising a cell.
35. The composition of claim 34 , wherein the cell is an antigen presenting cell.
36. The composition of claim 34 , wherein the cell is a cultured cell.
37. The composition of claim 23 , wherein the one or more HBV antigens comprise human HBV antigens.
38. The composition of claim 21 , wherein the composition comprises a monomer comprising an immune response domain and a target binding domain.
39. The composition of claim 38 , wherein the composition comprises a dimer of the monomer.
40. The composition of claim 21 , wherein a 6-His-peptide is linked to the target binding domain.