Fc fusion proteins for enhancing the immunogenicity of protein and peptide antigens
AssigneeMerck Patent GmbH
InventorsStephen D. Gillies, Kin-Ming Lo, John S. Wesolowski, Jr.
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AssigneeMerck Patent GmbH
InventorsStephen D. Gillies, Kin-Ming Lo, John S. Wesolowski, Jr.
Estimating the term…
Disclosed herein are methods and compositions for enhancing the immunogenicity of a preselected protein or peptide antigen in a mammal. Immunogenicity is enhanced by fusing the preselected antigen to an immunoglobulin heavy chain constant region to produce an Fc-antigen fusion protein. The Fc-antigen fusion proteins bind Fc receptors on the surface of antigen presenting cells, thereby targeting the antigen to the antigen presenting cells in the mammal. In addition, disclosed is a family of adjuvants, for example, an Fc-adjuvant fusion protein, for use in combination with the Fc-antigen fusion proteins to enhance or modulate a particular immune response against the preselected antigen.
A method of enhancing the immunogenicity of an antigen in a mammal, the method comprising:
A composition for eliciting an immune response against an antigen in a mammal, the composition comprising:
A method of enhancing the immunogenicity of an antigen in a mammal, the method comprising:
A method of enhancing the immunogenicity of an antigen in a mammal, the method comprising:
A composition comprising:
A composition comprising:
An anti-viral method comprising administering to a mammal an Fc-antigen fusion protein whose ability to bind an Fc receptor is not modified by mutation, wherein the antigen fusion protein lacks an immunoglobulin variable domain, the Fc-antigen fusion protein consisting of an HIV peptide linked to either polypeptide chain of an Fc region of an IgG molecule, the Fc region consisting of IgG hinge, CH2 and CH3 domains.
A method of enhancing the immunogenicity of an antigen in a mammal, the method comprising administering to a mammal an Fc-antigen fusion protein whose ability to bind an Fc receptor is not modified by mutation, wherein the antigen fusion protein lacks an immunoglobulin variable domain, the Fc-antigen fusion protein consisting of an HIV peptide linked to either polypeptide chain of an Fc region of an IgG molecule, the Fc region consisting of IgG hinge, CH2 and CH3 domains.
An anti-viral method, the method comprising administering an Fc-cytokine fusion protein whose ability to bind an Fc receptor is not modified by mutation, wherein the Fc-cytokine fusion protein lacks an immunoglobulin variable domain and comprises two polypeptide chains, one of which consists of one polypeptide chain of an immunoglobulin heavy chain constant region and the other of which consists of the other polypeptide chain of the immunoglobulin heavy chain constant region linked to a cytokine.
An anti-viral method, the method comprising administering an Fc-cytokine fusion protein whose ability to bind an Fc receptor is not modified by mutation, wherein the Fc-cytokine fusion protein lacks an immunoglobulin variable domain and comprises two polypeptide chains, one of which consists of one polypeptide chain of an immunoglobulin heavy chain constant region and the other of which consists of the other polypeptide chain of the immunoglobulin heavy chain constant region linked to a cytokine and to a viral protein.
An Fc-cytokine fusion protein whose ability to bind an Fc receptor is not modified by mutation, wherein the Fc-cytokine fusion protein lacks an immunoglobulin variable domain and comprises two polypeptide chains, one of which consists of one polypeptide chain of an immunoglobulin heavy chain constant region and the other of which consists of the other polypeptide chain of the immunoglobulin heavy chain constant region linked to a cytokine.
An Fc-cytokine fusion protein whose ability to bind an Fc receptor is not modified by mutation, wherein the Fc-cytokine fusion protein lacks an immunoglobulin variable domain and comprises two polypeptide chains, one of which consists of one polypeptide chain of an immunoglobulin heavy chain constant region and the other of which consists of the other polypeptide chain of the immunoglobulin heavy chain constant region linked to a cytokine and to a viral protein.
Dependencies are inferred from the claim text.