Peer-Reviewed Journal Details
Mandatory Fields
Hutchings, C. L.,Gilbert, S. C.,Hill, A. V.,Moore, A. C.
Journal of immunology (Baltimore, Md. : 1950)
Novel protein and poxvirus-based vaccine combinations for simultaneous induction of humoral and cell-mediated immunity
Optional Fields
Adenoviridae/immunology Animals Antibodies, Viral/biosynthesis Female Fowlpox virus/immunology Hepatitis B Antibodies/biosynthesis Hepatitis B Surface Antigens/administration & dosage/genetics Hepatitis B Vaccines/*administration & dosage Immunity, Cellular Immunization, Secondary Interferon Type II/biosynthesis Mice Mice, Inbred BALB C Research Support, Non-U.S. Gov't T-Lymphocytes/immunology Vaccines, Combined/administration & dosage Vaccines, DNA/*administration & dosage/genetics Vaccines, Synthetic/*administration & dosage Vaccinia virus/genetics/immunology Viral Vaccines/*administration & dosage/genetics
The presence of both cell-mediated and humoral immunity is important in protection from and clearance of a number of infectious pathogens. We describe novel vaccine regimens using combinations of plasmid DNA, poxvirus and protein to induce strong Ag-specific T cell and Ab responses simultaneously in a murine model. Intramuscular (i.m.) immunization with plasmid DNA encoding the middle Ag of hepatitis B (DNA) concurrently with a commercial hepatitis B virus (HBV) vaccine (Engerix-B) followed by boosting immunizations with both modified vaccinia virus Ankara (MVA) encoding the middle Ag of HBV and Engerix-B induced high levels of CD4(+) and CD8(+) T cells and high titer Ab responses to hepatitis B surface Ag (HbsAg). Substitution of Engerix-B with adjuvant-free rHBsAg induced similar T cell responses and greatly enhanced Ab levels. Repeated immunizations with recombinant or nonrecombinant MVA mixed with Ag induced higher titers of Abs compared with immunization with either Ag or Engerix-B further demonstrating this novel adjuvant effect of MVA. The poxviruses NYVAC, fowlpox (FP9) and ALVAC, and to a lesser extent, adenovirus, also displayed similar adjuvant properties when used in combination with rHBsAg. The use of poxviruses as an adjuvant for protein to concurrently induce Ag-specific T cells and Abs could be applied to the development of vaccines for many diseases, including HIV and malaria, where both cell mediated and humoral immunity may be important for protection.
Grant Details