免疫系统
生物
单核细胞增生李斯特菌
获得性免疫系统
T细胞
免疫
先天免疫系统
卵清蛋白
巨噬细胞
微生物学
免疫学
体外
细菌
遗传学
作者
Chyi‐Song Hsieh,S E Macatonia,Catherine S. Tripp,Stanley F. Wolf,Anne O’Garra,Kenneth M. Murphy
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1993-04-23
卷期号:260 (5107): 547-549
被引量:3128
标识
DOI:10.1126/science.8097338
摘要
Development of the appropriate CD4+ T helper (TH) subset during an immune response is important for disease resolution. With the use of naïve, ovalbumin-specific alpha beta T cell receptor transgenic T cell, it was found that heat-killed Listeria monocytogenes induced TH1 development in vitro through macrophage production of interleukin-12 (IL-12). Moreover, inhibition of macrophage production of IL-12 may explain the ability of IL-10 to suppress TH1 development. Murine immune responses to L. monocytogenes in vivo are of the appropriate TH1 phenotype. Therefore, this regulatory pathway may have evolved to enable innate immune cells, through interactions with microbial pathogens, to direct development of specific immunity toward the appropriate TH phenotype.
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