Castro A, Bemer V, Nóbrega A, Coutinho A, Truffa-Bachi P
Unité d'Immunobiologie, CNRS URA 1961, Institut Pasteur, Paris, France.
Eur J Immunol. 1998 Feb;28(2):488-95. doi: 10.1002/(SICI)1521-4141(199802)28:02<488::AID-IMMU488>3.0.CO;2-R.
Lipopolysaccharide (LPS) from gramnegative bacteria is a well-known T cell-independent B lymphocyte mitogen and macrophage/monocyte activator. While the conventional view holds that LPS is ignored by T cells, we report here that administration of LPS to mice activates all B cells, but also engages most CD4 and CD8 T cells, as measured by the expression of the activation markers CD69 and CD25 and by size increase. T cells recruited in endotoxin-treated mice showed, following in vitro stimulation by concanavalin A, altered patterns of cytokine production. In vivo, massive T cell apoptosis was evidenced in the days following LPS exposure. The present observation may contribute novel insights into the mechanisms of endotoxin shock and of the immunological consequences of gram-negative infections.
革兰氏阴性菌的脂多糖(LPS)是一种众所周知的非T细胞依赖性B淋巴细胞有丝分裂原和巨噬细胞/单核细胞激活剂。虽然传统观点认为T细胞会忽略LPS,但我们在此报告,给小鼠注射LPS会激活所有B细胞,同时也会使大多数CD4和CD8 T细胞被激活,这可通过激活标志物CD69和CD25的表达以及细胞大小增加来衡量。在内毒素处理的小鼠中募集的T细胞,在体外受伴刀豆球蛋白A刺激后,细胞因子产生模式发生了改变。在体内,LPS暴露后的几天内可明显观察到大量T细胞凋亡。本观察结果可能为内毒素休克机制以及革兰氏阴性菌感染的免疫后果提供新的见解。