Protective CD4 + and CD8 + T Cells against Influenza Virus Induced by Vaccination with Nucleoprotein DNA

Author:

Ulmer Jeffrey B.1,Fu Tong-Ming1,Deck R. Randall1,Friedman Arthur1,Guan Liming1,DeWitt Corrille1,Liu Xu1,Wang Su1,Liu Margaret A.1,Donnelly John J.1,Caulfield Michael J.1

Affiliation:

1. Department of Virus and Cell Biology, Merck Research Laboratories, West Point, Pennsylvania 19486

Abstract

ABSTRACT DNA vaccination is an effective means of eliciting both humoral and cellular immunity, including cytotoxic T lymphocytes (CTL). Using an influenza virus model, we previously demonstrated that injection of DNA encoding influenza virus nucleoprotein (NP) induced major histocompatibility complex class I-restricted CTL and cross-strain protection from lethal virus challenge in mice (J. B. Ulmer et al., Science 259:1745–1749, 1993). In the present study, we have characterized in more detail the cellular immune responses induced by NP DNA, which included robust lymphoproliferation and Th1-type cytokine secretion (high levels of gamma interferon and interleukin-2 [IL-2], with little IL-4 or IL-10) in response to antigen-specific restimulation of splenocytes in vitro. These responses were mediated by CD4 + T cells, as shown by in vitro depletion of T-cell subsets. Taken together, these results indicate that immunization with NP DNA primes both cytolytic CD8 + T cells and cytokine-secreting CD4 + T cells. Further, we demonstrate by adoptive transfer and in vivo depletion of T-cell subsets that both of these types of T cells act as effectors in protective immunity against influenza virus challenge conferred by NP DNA.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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