Journals of Gerontology Series A: Biological Sciences and Medical Sciences Large Type Edition
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Journals of Gerontology Series A: Biological Sciences and Medical Sciences, Vol 54, Issue 3 B116-B123, Copyright © 1999 by The Gerontological Society of America


JOURNAL ARTICLE

The age-dependent cytokine production by murine CD8+ T cells as determined by four-color flow cytometry analysis

XY Mu and ML Thoman
Department of Immunology, Sidney Kimmel Cancer Center, San Diego, California, USA.

Flow cytometry has been used to simultaneously examine intracellular cytokine production and expression of CD44 and CD45RB by murine CD8+ T cells derived from young (2-3 months) or aged (18-22 months) mice. Cytokine production by aged CD8+ T cells differs from that by CD8+ T cells derived from young animals in that a significantly higher percentage of the aged can be triggered to produce interleukin (IL)-4, interferon (IFN)-gamma, and tumor necrosis factor alpha (TNF alpha). Conversely, a greater fraction of young CD8+ T cells produce IL-2. Aged mice not only have a higher percentage of CD8+/CD44hi T cells, but also a larger fraction of these cells are IFN-gamma+ and IL-4+, while a lower fraction are IL-2+ than is observed in young CD8+/CD44hi T cells. In terms of relative contribution to total cytokine synthesis, a greater fraction of CD8+ T cells produce IFN-gamma and IL-4 than in CD4+ T cells, whereas CD4+ T cells are the major producers of IL-2.


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J. Lustgarten, A. L. Dominguez, and M. Thoman
Aged Mice Develop Protective Antitumor Immune Responses with Appropriate Costimulation
J. Immunol., October 1, 2004; 173(7): 4510 - 4515.
[Abstract] [Full Text] [PDF]


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S. P. Li, Z. Cai, W. Shi, A. Brunmark, M. Jackson, and P.-J. Linton
Early Antigen-Specific Response by Naive CD8 T Cells Is Not Altered with Aging
J. Immunol., June 15, 2002; 168(12): 6120 - 6127.
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