Augmentation of the CD8+ T cell response by IFN-γ in IL-12-deficient mice during Toxoplasma gondii infection

被引:0
|
作者
Ely, KH
Kasper, LH
Khan, IA
机构
[1] Dartmouth Med Sch, Dept Med, Lebanon, NH 03756 USA
[2] Dartmouth Med Sch, Dept Physiol, Lebanon, NH 03756 USA
[3] Dartmouth Med Sch, Dept Microbiol, Lebanon, NH 03756 USA
来源
JOURNAL OF IMMUNOLOGY | 1999年 / 162卷 / 09期
关键词
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The importance of IFN-gamma in regulating the host CD8(+) T cell response during microbial infection has not been delineated. Mice deficient for the p40 chain of the IL-12 heterodimer have impaired IFN-gamma production and are susceptible to infection with the intracellular parasite Toxoplasma gondii. The administration of exogenous ITN-gamma to parasite-infected p40(-/-) mice increases survival and up-regulates the depressed CD8(+) T cell response following infection. CD8(+) T cells isolated from cytokine-treated p40-/- mice exhibit an increase in both precursor CTL frequency and IFN-gamma production compared with untreated controls. The enhancement of the CD8(+) T cell response is independent of CD4(+) T cell help. These CD8(+) T cells induce protective immunity against a lethal challenge when adoptively transferred into naive p40(-/-) and IFN-gamma(-/-) mice. These observations indicate that IFN-gamma can regulate the CD8(+) T cell response during T. gondii infection.
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收藏
页码:5449 / 5454
页数:6
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