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Research Article Free access | 10.1172/JCI118843

IL-12 in conjunction with dendritic cells enhances antiviral CD8+ CTL responses in vitro.

N Bhardwaj, R A Seder, A Reddy, and M V Feldman

Rockefeller University, New York 10021, USA.

Find articles by Bhardwaj, N. in: PubMed | Google Scholar

Rockefeller University, New York 10021, USA.

Find articles by Seder, R. in: PubMed | Google Scholar

Rockefeller University, New York 10021, USA.

Find articles by Reddy, A. in: PubMed | Google Scholar

Rockefeller University, New York 10021, USA.

Find articles by Feldman, M. in: PubMed | Google Scholar

Published August 1, 1996 - More info

Published in Volume 98, Issue 3 on August 1, 1996
J Clin Invest. 1996;98(3):715–722. https://doi.org/10.1172/JCI118843.
© 1996 The American Society for Clinical Investigation
Published August 1, 1996 - Version history
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Abstract

CD8+ cytolytic T lymphocytes (CTLs) are important mediators for resistance to infections and malignant diseases. IL-12 enhances proliferative and cytolytic responses by killer cells, but its function in the generation of human antiviral CD8+ T cell responses has not been defined. We therefore evaluated the role of IL-12 in the generation of CTLs to influenza-infected dendritic cells. IL-12 was not detectable in supernatants of infected-dendritic cells, or during CTL generation. Furthermore, anti-IL-12 antibody did not block CTL generation. However, exogenous IL-12 (30-300 pg/ml) enhanced CD8+ T cell proliferative and cytolytic responses. The effect was greatest in individuals with weak reactivity to influenza virus or at antigen-presenting cell (APC):T cell ratios of 1:100 or less. IL-12 augmented interferon-gamma production during CTL generation. The CTL enhancing effects of the cytokine, however, could not be blocked by neutralizing anti-interferon-gamma antibody. Together with IL-12, antigen-pulsed dendritic cells may be a useful approach for boosting CTL responses against infectious agents and malignancies.

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