Journal
JOURNAL OF EXPERIMENTAL MEDICINE
Volume 201, Issue 7, Pages 1053-1059Publisher
ROCKEFELLER UNIV PRESS
DOI: 10.1084/jem.20041463
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Funding
- NIAID NIH HHS [R21 AI027028, AI-52351, R01 AI027028, R21 AI052351, AI-27028, R01 AI052351, R56 AI027028] Funding Source: Medline
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Interferon-gamma (IFN gamma) is important in regulating the adaptive immune response, and most current evidence suggests that it exerts a negative (proapoptotic) effect on CD8(+) T cell responses. We have developed a novel technique of dual adoptive transfer, which allowed us to precisely compare, in normal mice, the in vivo antiviral responses of two T cell populations that differ only in their expression of the IFN gamma receptor. We use this technique to show that, contrary to expectations, IFN gamma strongly stimulates the development of CD8(+) T cell responses during an acute viral infection. The stimulatory effect is abrogated in T cells lacking the IFN gamma receptor, indicating that the cytokine acts directly upon CD8(+) T cells to increase their abundance during acute viral infection.
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