IL-15 is a growth factor and an activator of CD8 memory T cells

被引:71
作者
Weng, NP
Liu, KB
Catalfamo, M
Li, Y
Henkart, PA
机构
[1] NIA, Immunol Lab, NIH, Baltimore, MD 21224 USA
[2] NCI, Expt Immunol Branch, NIH, Bethesda, MD 20892 USA
来源
MICROARRAYS, IMMUNE RESPONSES AND VACCINES | 2002年 / 975卷
关键词
IL-15; memory CD8 T cells; TCR; microarray; cytotoxicity;
D O I
10.1111/j.1749-6632.2002.tb05940.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Memory lymphocytes, arising from naive lymphocytes after antigenic stimulation and being long-lived, are the cellular basis for immunological memory. Recent studies of CD8 T cells suggest that generation of CD8 memory T cells requires the engagement of T cell antigen receptors (TCR) with antigen, yet the maintenance of CD8 memory T cells appears to be dependent on cytokines, such as IL-15, independent of TCR. Although considerable progress has been made in understanding the molecular and cellular events of TCR-induced differentiation and proliferation in the past decade, less is known about the mechanisms of IL-15 action. From a kinetic and comparative analysis of the responses of memory phenotype CD8 T cells to IL-15 and TCR stimulation in vitro, we found that IL-15 and anti-CD3 induce highly similar responses in memory phenotype CD8 T cells as measured by general gene expression profiles, synthesis of effector molecules (IFNgamma, TNFbeta, granzyme B and perforin), induction of cytotoxicity, and cellular proliferation. These findings indicate that IL-15 is not only a growth factor but also an antigen-independent activator for CD8 memory T cells.
引用
收藏
页码:46 / 56
页数:11
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