Chimeric adenoviral vectors
The present invention provides chimeric adenoviral vectors and methods for using the vectors to elicit an immune response to an antigen of interest.
1. A method for eliciting an immune response, said method comprising administering an immunogenic composition to a mammalian subject, said immunogenic composition comprising:
(a) a chimeric viral vector comprising a first promoter operably linked to a nucleic acid encoding a heterologous polypeptide;
(b) a non-specific immune response enhancer selected from dsRNA and a dsRNA mimetic; and
(c) a pharmaceutically acceptable carrier, wherein the immune response is directed against the heterologous polypeptide, and wherein the route of administration is selected from the group consisting of: oral, intranasal, and mucosal.
2. The method of claim 1 , wherein the immune response enhancer is encoded on the chimeric viral vector under the control of a second promoter.
3. The method of claim 2 , wherein the first promoter and second promoter are the same.
4. The method of claim 2 , wherein the first promoter and second promoter are different.
5. The method of claim 1 , wherein the heterologous polypeptide is a viral antigen.
6. The method of claim 5 , wherein the viral antigen is from a virus selected from influenza, HIV, HPV, Epstein Barr virus, Herpes simplex virus, hepatitis A, hepatitis B, hepatitis C, hepatitis E, mumps virus, rubella virus, measles virus, poliovirus, smallpox virus, rabies virus, and Variella-zoster virus.
7. The method of claim 1 , wherein the heterologous polypeptide is a bacterial antigen.
8. The method of claim 1 , wherein the heterologous polypeptide is a fungal antigen.
9. A method for eliciting an immune response, said method comprising administering an immunogenic composition to a mammalian subject, said immunogenic composition comprising a chimeric adenoviral expression vector comprising:
(a) a first promoter operably linked to a nucleic acid encoding a toll-like receptor-3 (TLR-3) agonist, wherein the TLR-3 agonist is a double stranded RNA (dsRNA); and
(b) a second promoter operably linked to a nucleic acid encoding a heterologous polypeptide; and
(c) a pharmaceutically acceptable carrier,
wherein the immune response is directed against the heterologous polypeptide, and wherein the route of administration is oral.