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通过多克隆T细胞激活剂激活的淋巴细胞获得对体外初次免疫反应的抑制和辅助作用的实验条件。

Experimental conditions for obtaining suppressor and helper effects on the primary in vitro immune response by lymphocytes activated by polyclonal T-cell activators.

作者信息

Nespoli L, Möller G, Waterfield D, Ekstedt R

机构信息

Division of Immunobiology, Karolinska Institute, Wallenberglaboratory Lilla Freskati, Stockholm, Sweden.

出版信息

J Exp Med. 1977 Mar 1;145(3):631-43. doi: 10.1084/jem.145.3.631.

Abstract

The effect of the polyclonal T-cell activators (PTA) Con A and PHA on the specific immune response to sheep red blood cells (SRC) was studied. Addition of PTA either enhanced or suppressed the anti-SRC response, and two variables were found to affect the results: time of addition of the PTA and the strength of the response in control cultures not given PTA. If the response was high, even suboptimal PTA concentrations induced suppressive effects, but if the control response was low, due to deficient batches of sera or because of the absence of serum, the addition of PTA increased the response or restored it to normal levels. Suppression could be obtained if the PTA were added before or at the same time as the antigen and required high (optimal) PTA concentrations. If addition was delayed for 12-24 h the suppressive effects disappeared and previously suppressive concentrations of the PTA now caused an enhanced response. Analogous results were obtained if preactivated lymphocytes were added to the cultures instead of soluble PTA. Neither Con A, PHA, or lymphocytes preactivated by these PTA suppressed the polyclonal response induced by LPS or PPD. Irrespective of the time of addition and the culture conditions, enhancement of the anti-SRC response occurred at lower PTA concentrations than suppression. It was concluded that suppressor T cells, if they exist, do not act on B cells, but rather on helper cells needed for induction of thymus-dependent responses. The findings in this system are not compatible with the existence of a specific subset of suppressor T cells, but rather with the notion that suppression is caused by too much help.

摘要

研究了多克隆T细胞激活剂(PTA)刀豆蛋白A(Con A)和植物血凝素(PHA)对绵羊红细胞(SRC)特异性免疫反应的影响。添加PTA可增强或抑制抗SRC反应,发现有两个变量影响结果:PTA的添加时间以及未添加PTA的对照培养物中的反应强度。如果反应强烈,即使次优浓度的PTA也会诱导抑制作用,但如果对照反应较弱,原因是血清批次不足或无血清,则添加PTA会增强反应或将其恢复到正常水平。如果在抗原之前或同时添加PTA可获得抑制作用,且需要高(最佳)浓度的PTA。如果延迟添加12 - 24小时,抑制作用消失,先前具有抑制作用浓度的PTA现在会引起反应增强。如果将预激活的淋巴细胞添加到培养物中而不是可溶性PTA,也会得到类似结果。Con A、PHA或由这些PTA预激活的淋巴细胞均未抑制脂多糖(LPS)或结核菌素纯蛋白衍生物(PPD)诱导的多克隆反应。无论添加时间和培养条件如何,在比抑制作用更低的PTA浓度下就会出现抗SRC反应增强。得出的结论是,抑制性T细胞(如果存在的话)并不作用于B细胞,而是作用于诱导胸腺依赖性反应所需的辅助性细胞。该系统中的发现与特异性抑制性T细胞亚群的存在不相符,而是与抑制是由过多辅助作用引起的观点相符。

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