Immunoglobulin chimeric monomer-dimer hybrids
US-2017266309-A1 · Sep 21, 2017 · US
US10329338B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10329338-B2 |
| Application number | US-201514789628-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 1, 2015 |
| Priority date | May 3, 2006 |
| Publication date | Jun 25, 2019 |
| Grant date | Jun 25, 2019 |
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A synergistic adjuvant is provided comprising synergistically effective amounts of at least one type 1 interferon and at least one CD40 agonist, wherein these moieties may be in the same or separate compositions. In addition, fusion proteins and DNA conjugates which contain a type 1 interferon/CD40 agonist/antigen combination are provided. The use of these compositions, protein and DNA conjugates as immune adjuvants for treatment of various chronic diseases such as HIV infection and for enhancing the efficacy of vaccines (prophylactic and therapeutic) is also provided.
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The invention claimed is: 1. A nucleic acid construct which encodes polypeptides which in combination elicit a synergistic effect on CD70 expression by dendritic cells and/or CD8 + T proliferation, activation or CD8 + T cell immune responses comprising: (i) a nucleic acid encoding an agonistic anti-CD40 antibody or agonistic binding fragment thereof, wherein said agonistic anti-CD40 antibody is a monoclonal antibody selected from CD40.4 (5c3) and S2C6; and (ii) a nucleic acid sequence encoding a type 1 interferon; and (iii) optionally a nucleic acid sequence encoding a desired antigen; wherein the sequences (i), (ii) and (iii) if present are operably linked to the same or different transcription regulatory sequences. 2. The nucleic acid construct of claim 1 wherein: (1) wherein the sequences of (i) and (ii) are linked together, directly or indirectly, in either order; or (2) the sequences of (i) and (iii) are linked together, directly or indirectly, in either order; or (3) the sequences of (ii) and (iii) are linked together, directly or indirectly, in either order; or (4) wherein the sequences of (i), (ii) and (iii) are linked together, directly or indirectly, in any order. 3. The nucleic acid construct of claim 2 , wherein the type 1 interferon is interferon α, β, tao, epsilon, zeta or omega. 4. The nucleic acid construct of claim 2 , wherein the antigen is a cancer antigen or an infectious agent antigen selected from a viral, bacterial, fungal or parasitic antigen, or is an autoantigen or other human antigen the expression of which correlates with or is involved in a chronic human disease. 5. The nucleic acid constrict of claim 1 , wherein the type 1 interferon is interferon α, β, tao, epsilon, zeta or omega. 6. The nucleic acid constrict of claim 1 wherein the antigen is a cancer antigen or an infectious agent antigen selected from a viral, bacterial, fungal or parasitic antigen, or is an autoantigen or other human antigen the expression of which correlates with or is involved in a chronic human disease. 7. The nucleic acid constrict of claim 1 wherein all three of said moieties are directly or indirectly linked to one another. 8. The nucleic acid constrict of claim 1 wherein the nucleic acid encoding the antigen and nucleic acid encoding the type 1 interferon are directly or indirectly linked to one another. 9. The nucleic acid constrict of claim 1 wherein the antigen and the agonistic anti-CD40 antibody or agonistic binding fragment thereof are directly or indirectly linked to one another. 10. The nucleic acid constrict of claim 1 wherein the nucleic acid encoding the type 1 interferon and the nucleic acid encoding the agonistic anti-CD40 or agonistic binding fragment thereof are indirectly linked to one another. 11. The nucleic acid construct of claim 1 , wherein the type 1 interferon is alpha or beta interferon. 12. The nucleic acid construct of claim 1 , wherein the antigen is a cancer antigen. 13. The nucleic acid construct of claim 1 , wherein the antigen is a viral cancer antigen.
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