TY - JOUR
T1 - Characterization of in vivo primary and secondary CD8+ T cell responses induced by recombinant influenza and vaccinia viruses
AU - Murata, Kenichiro
AU - García-Sastre, Adolfo
AU - Tsuji, Moriya
AU - Rodrigues, Mauricio
AU - Rodriguez, Dolores
AU - Rodriguez, Juan Ramon
AU - Nussenzweig, Ruth S.
AU - Palese, Peter
AU - Esteban, Mariano
AU - Zavala, Fidel
N1 - Funding Information:
We thank Dr. Jerome L. Schulman for helpful suggestions and discussions. We also thank Chui Ng, John Hirst, Scott Kerns, and Ricardo Renvill for excellent technical assistance. This work was supported by grants from the National Institutes of Health (AI-27458, AI-36526), Agency for International Development, and a grant (A.G.-S.) from the Stony Wold-Herbert Fund.
PY - 1996/10/10
Y1 - 1996/10/10
N2 - We characterized the in vivo primary and secondary murine CD8+ T cell responses induced by immunization with influenza and vaccinia viruses, which were engineered to express the same H-2K(k)- and H-2K(d)-restricted epitopes. Our results show that the induction and magnitude of the primary CD8+ T cell response closely depends on the viral dose used for immunization, while it is not affected by the route of immunization. The induction of secondary CD8+ T cell responses appears to be highly restricted, as suggested by the lack of in vivo expansion of antigen-specific CD8+ T cells after repeated immunization with the same virus. In contrast, a 20- to 30-fold increase in the frequency of antigen-specific CD8+ T cells could be induced after combined immunization with recombinant influenza and vaccinia viruses. These findings may provide the basis for the development of new prophylactic and therapeutic strategies to prevent or control intracellular infections and certain malignancies.
AB - We characterized the in vivo primary and secondary murine CD8+ T cell responses induced by immunization with influenza and vaccinia viruses, which were engineered to express the same H-2K(k)- and H-2K(d)-restricted epitopes. Our results show that the induction and magnitude of the primary CD8+ T cell response closely depends on the viral dose used for immunization, while it is not affected by the route of immunization. The induction of secondary CD8+ T cell responses appears to be highly restricted, as suggested by the lack of in vivo expansion of antigen-specific CD8+ T cells after repeated immunization with the same virus. In contrast, a 20- to 30-fold increase in the frequency of antigen-specific CD8+ T cells could be induced after combined immunization with recombinant influenza and vaccinia viruses. These findings may provide the basis for the development of new prophylactic and therapeutic strategies to prevent or control intracellular infections and certain malignancies.
UR - http://www.scopus.com/inward/record.url?scp=0008497139&partnerID=8YFLogxK
U2 - 10.1006/cimm.1996.0255
DO - 10.1006/cimm.1996.0255
M3 - Article
C2 - 8871605
AN - SCOPUS:0008497139
SN - 0008-8749
VL - 173
SP - 96
EP - 107
JO - Cellular Immunology
JF - Cellular Immunology
IS - 1
ER -