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由特异性激活的双致敏淋巴细胞产生的一种因子介导的体液免疫反应的短暂抑制。

Transient suppression of the humoral immune response mediated by a factor derived from specifically activated, doubly primed lymphoid cells.

作者信息

Kempf K E, Rubin A S

出版信息

J Immunol. 1977 Aug;119(2):517-23.

PMID:886185
Abstract

In cultures of sheep erythrocyte- (SRBC) stimulated spleen cells from mice immunized with tetanus toxoid (TT) and horse erythrocytes (HRBC) 30 to 90 days earlier, the addition of both HRBC (day 0) and TT (day 2) resulted in significant suppression of the anti-SRBC plaque-forming cell (PFC) response compared to the response of similar cultures maintained without the priming antigens. The observed inhibition was due to the presence of a soluble factor that was released into the supernatant fluid of the specifically stimulated, primed population of lymphoid cells between 72 and 120 hr after culture initiation. The active mediator, a macromolecule of approximately 24,000 daltons as determined by gel filtration over Sephadex G-150 and Ultrogel AcA 44, was suppressive when added within 24 hr, but not 48 hr, of assay for PFC against the reference SRBC antigen. The transiently acting soluble suppressor (TASS) was not overtly cytotoxic since total cell recovery and viability were unaffected in its presence. The results presented here are discussed in relation to a possible mechanism of action in which the negative regulation of immunoglobulin production is favored once a minimum level of immune reactivity is reached.

摘要

在对30至90天前用破伤风类毒素(TT)和马红细胞(HRBC)免疫的小鼠的绵羊红细胞(SRBC)刺激的脾细胞培养物中,与未添加致敏抗原的类似培养物的反应相比,添加HRBC(第0天)和TT(第2天)均导致抗SRBC空斑形成细胞(PFC)反应受到显著抑制。观察到的抑制作用归因于一种可溶性因子的存在,该因子在培养开始后72至120小时之间释放到特异性刺激的致敏淋巴细胞群体的上清液中。通过在Sephadex G - 150和Ultrogel AcA 44上进行凝胶过滤测定,活性介质是一种分子量约为24,000道尔顿的大分子,在针对参考SRBC抗原的PFC测定的24小时内添加时具有抑制作用,但在48小时内添加则无抑制作用。短暂作用的可溶性抑制因子(TASS)没有明显的细胞毒性,因为在其存在下总细胞回收率和活力不受影响。本文给出的结果结合一种可能的作用机制进行了讨论,即在达到最低免疫反应水平后,免疫球蛋白产生的负调节受到青睐。

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