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同种异体反应性细胞毒性T淋巴细胞的产生:经单核细胞增多性李斯特菌免疫的小鼠腹腔细胞除产生白细胞介素1和白细胞介素2外,还产生T细胞和巨噬细胞辅助因子。

Generation of alloreactive cytotoxic T lymphocytes: production of T cell and macrophage helper factors in addition to IL 1 and IL 2 by peritoneal cells from mice immunized to Listeria monocytogenes.

作者信息

Finke J H, Sharma S D, Scott J W

出版信息

J Immunol. 1981 Dec;127(6):2354-61.

PMID:6795272
Abstract

We investigate the production and biological activity of soluble helper factors produced by peritoneal T cells and macrophage derived from mice primed in vivo with Listeria monocytogenes. Supernatant fluids from co-cultures of these immune T cells and activated macrophages contained Interleukin 1 (IL 1) and Interleukin 2 (IL 2), and had the ability to assist the generation of cytotoxic T lymphocytes (CTL) from a population of nylon wool nonadherent spleen cells sensitized to allogeneic heat-treated thymocytes. The ability to assist CTL development involved T cell and macrophage factors in addition to IL 1 and IL 2. Immune T cells cultured alone produced a factor, devoid of significant IL 2 activity, that assisted CTL development only if adherent cells were present in the responding population. Activated macrophage produced a 38,000 dalton component, distinct from IL 1 on the basis of m.w., that assisted the development of CTL from nylon wool nonadherent splenic cells. Supernatants fluids from co-cultures of immune T cells and allogeneic, nonactivated macrophage contained a CTL helper factor but did not contain IL 1 or IL 2 activities. In contrast, supernatant fluids from co-cultures of immune T cells and syngeneic, nonactivated macrophage contained all 3 activities. This suggests a genetic restriction for the production of IL 1 and IL 2 that does not restrict the production of a CTL helper factor. These results demonstrate that T cell- and macrophage-derived helper factors distinct from IL 1 and IL 2 participate in the development of CTL.

摘要

我们研究了由经体内单核细胞增多性李斯特菌致敏的小鼠腹膜T细胞和巨噬细胞产生的可溶性辅助因子的产生及生物学活性。这些免疫T细胞与活化巨噬细胞共培养的上清液中含有白细胞介素1(IL-1)和白细胞介素2(IL-2),并且有能力辅助从对同种异体热处理胸腺细胞致敏的尼龙毛非黏附脾细胞群体中产生细胞毒性T淋巴细胞(CTL)。辅助CTL发育的能力除了涉及IL-1和IL-2外,还涉及T细胞和巨噬细胞因子。单独培养的免疫T细胞产生一种因子,该因子缺乏显著的IL-2活性,只有当应答群体中存在黏附细胞时,它才能辅助CTL发育。活化的巨噬细胞产生一种38000道尔顿的成分,基于分子量与IL-1不同,它能辅助尼龙毛非黏附脾细胞产生CTL。免疫T细胞与同种异体、未活化巨噬细胞共培养的上清液含有一种CTL辅助因子,但不含有IL-1或IL-2活性。相比之下,免疫T细胞与同基因、未活化巨噬细胞共培养的上清液含有所有三种活性。这表明IL-1和IL-2的产生存在基因限制,但这并不限制CTL辅助因子的产生。这些结果表明,不同于IL-1和IL-2的T细胞和巨噬细胞衍生的辅助因子参与了CTL的发育。

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