FcRn-targeted mucosal vaccination against RSV
AssigneeUniversity of Maryland, College Park
InventorsXiaoping Zhu, Weizhong Li
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AssigneeUniversity of Maryland, College Park
InventorsXiaoping Zhu, Weizhong Li
Estimating the term…
Disclosed are peptides comprising a monomeric Fc fragment of an immunoglobulin recognized by a neonatal receptor (FcRn); a modified pre-fusion respiratory syncytia virus (RSV) F protein; and a trimerization domain. Disclosed are nucleic acid sequences capable of encoding peptides comprising a monomeric Fc fragment of an immunoglobulin recognized by a neonatal receptor (FcRn); a modified pre-fusion respiratory syncytia virus (RSV) F protein; and a trimerization domain. Also disclosed are methods for eliciting a protective immune response against RSV comprising administering to a subject an effective amount of a composition comprising a monomeric Fc fragment of an immunoglobulin recognized by FcRn; a modified pre-fusion RSV F protein; and a trimerization domain, wherein the administering is to a mucosal epithelium.
A peptide comprising
A method for eliciting a protective immune response against RSV comprising administering to a subject an effective amount of a composition comprising a fusion protein, wherein the fusion protein comprises a monomeric Fc fragment of an immunoglobulin recognized by a FcRn, wherein the monomeric Fc fragment comprises an amino acid mutation that prevents dimer formation with other monomeric Fc fragments, wherein the monomeric Fc fragment of an immunoglobulin recognized by a FcRn comprises a mutation in the cysteine residues responsible for dimer formation;
A method of treating a subject exposed to RSV or at risk of being exposed to RSV comprising administering to the subject an effective amount of a composition comprising a fusion protein, wherein the fusion protein comprises a monomeric Fc fragment of an immunoglobulin recognized by a FcRn, wherein the monomeric Fc fragment comprises an amino acid mutation that prevents dimer formation with other monomeric Fc fragments, wherein the monomeric Fc fragment of an immunoglobulin recognized by a FcRn comprises a mutation in the cysteine residues responsible for dimer formation;
Dependencies are inferred from the claim text.