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葡萄球菌肠毒素对体外初次免疫反应的影响。

The effect of staphylococcal enterotoxins on the primary in vitro immune response.

作者信息

Smith B G, Johnson H M

出版信息

J Immunol. 1975 Aug;115(2):575-8.

PMID:1097520
Abstract

Staphylococcal enterotoxins, like several plant lectins, have been shown to stimulate mitogenic activity and lymphokine production in lymphocytes. The effect of enterotoxins A and B on the primary in vitro plaque-forming cell (PFC) response of mouse (C57BL/6) spleen cells to sheep red blood cells (SRBC) was examined. PFC responses in 4- or 5-day cultures were inhibited greater than 90% by 0.1 mug enterotoxin A and by 3- to 6-mug enterotoxin B when the toxins were added to the cultures either at the time of SRBC addition or 24 hr before. Both enterotoxins A and B were shown to be T lymphocyte mitogens. Kinetic data indicated that the enterotoxins (10 mug) inhibited the PFC response as early as day 3, but were relatively more inhibitory at days 4 and 5. The PFC response was inhibited when enterotoxins were added to cultures at the same time as antigen or a day later; it was enhanced when added at day 2; and it was unaffected when added at day 3 of 4-day cultures. Further, the presence of enterotoxin A during the first 24 hr of culture and subsequent removal was still as effective in inhibiting the PFC response as when it was present throughout the culture period. The PFC inhibitory properties of enterotoxins appear, then, to affect some early event(s) in the in vitro immune response. Alpha-methyl-D-mannopyranoside blocked the PFC inhibitory effect of concanavalin A (con A), but it had no effect on enterotoxin A. The two mitogens appear, then, to react with different receptors on the lymphocytes or to differ in the dynamics of their reactivity. The effects of staphylococcal enterotoxins on the PFC response of spleen cells were remarkably similar to those reported for lectins such as con A. Enterotoxins are structurally simpler than con A and should therefore be quite useful in studying various biologic activities of lymphocytes.

摘要

葡萄球菌肠毒素与几种植物凝集素一样,已被证明能刺激淋巴细胞的有丝分裂活性和淋巴因子产生。研究了肠毒素A和B对小鼠(C57BL/6)脾细胞对绵羊红细胞(SRBC)的体外初次空斑形成细胞(PFC)反应的影响。当在添加SRBC时或提前24小时将毒素添加到培养物中时,4或5天培养物中的PFC反应被0.1微克肠毒素A和3至6微克肠毒素B抑制超过90%。肠毒素A和B均被证明是T淋巴细胞有丝分裂原。动力学数据表明,肠毒素(10微克)早在第3天就抑制了PFC反应,但在第4天和第5天抑制作用相对更强。当肠毒素与抗原同时或在抗原添加一天后添加到培养物中时,PFC反应受到抑制;在第2天添加时反应增强;在4天培养的第3天添加时则不受影响。此外,在培养的最初24小时存在肠毒素A并随后去除,其抑制PFC反应的效果与在整个培养期间都存在时一样。因此,肠毒素的PFC抑制特性似乎影响了体外免疫反应中的一些早期事件。α-甲基-D-甘露吡喃糖苷可阻断伴刀豆球蛋白A(Con A)的PFC抑制作用,但对肠毒素A没有影响。那么,这两种有丝分裂原似乎与淋巴细胞上的不同受体发生反应,或者在反应动力学上有所不同。葡萄球菌肠毒素对脾细胞PFC反应的影响与Con A等凝集素报道的影响非常相似。肠毒素在结构上比Con A更简单,因此在研究淋巴细胞的各种生物学活性方面应该非常有用。

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