Delineation of the function of a major γδ T cell subset during infection

被引:42
作者
Andrew, EM
Newton, DJ
Dalton, JE
Egan, CE
Goodwin, SJ
Tramonti, D
Scott, P
Carding, SR
机构
[1] Univ Leeds, Sch Biochem & Microbiol, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA
基金
英国惠康基金;
关键词
D O I
10.4049/jimmunol.175.3.1741
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
gamma delta T cells play important but poorly defined roles in pathogen-induced immune responses and in preventing chronic inflammation and pathology. A major obstacle to defining their function is establishing the degree of functional redundancy and heterogeneity among gamma delta T cells. Using mice deficient in V gamma 1(+) T cells which are a major component of the gamma delta T cell response to microbial infection, a specific immunoregulatory role for V gamma 1(+) T cells in macrophage and gamma delta T cell homeostasis during infection has been established. By contrast, V gamma 1(+) T cells play no significant role in pathogen containment or eradication and cannot protect mice from immune-mediated pathology. Pathogen-elicited V gamma 1(+) T cells also display different functional characteristics at different stages of the host response to infection that involves unique and different populations of V gamma 1(+) T cells. These findings, therefore, identify distinct and nonoverlapping roles for gamma delta T cell subsets in infection and establish the complexity and adaptability of a single population of gamma delta T cells in the host response to infection that is not predetermined, but is, instead, shaped by environmental factors.
引用
收藏
页码:1741 / 1750
页数:10
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