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破伤风类毒素免疫后对人体混合淋巴细胞反应的抑制作用。

Inhibition of mixed lymphocyte reactions in humans after immunization with tetanus toxoid.

作者信息

Février M, Bona C, Eyquem A, Liacopoulos P

出版信息

Transplantation. 1977 Mar;23(3):199-209. doi: 10.1097/00007890-197703000-00001.

Abstract

Immunization of humans with tetanus toxoid (TT) results in an inhibition of the reactivity of peripheral lymphocytes to TT as well as to one-way mixed lymphocyte reaction. The strongest inhibition was observed in cells taken 3 or 7 days after immunization. These reactivities reappeared on the 14th day and reached their initial levels by the 21st day after immunization. The role of the various cell types was studied by culturing separately purified T or B lymphocytes taken on day 7 after immunization. B cells alone are not stimulated by TT or allogeneic cells. Purified T cells are stimulated much more than the initial total cell population. When B cells were mixed and cultured along with T cells, a suppressor effect upon stimulation appeared which reduced 3H-thymidine incorporation to the levels of the initial population. Treatment with 5-bromodeoxyuridine followed by exposure to light of cells stimulated with TT abrogated their ability to respond to subsequent stimulation with TT; whereas the responsiveness of treated cells to allogeneic lymphocytes was not significantly affected and vice versa. These results suggest that each stimulator activated a separate population of T cells but that in vivo immunization provoked the development of both a specific and nonspecific suppressor activity. Most probably this suppressor activity was brought about by adherent, surface Ig-bearing (B) cells.

摘要

用破伤风类毒素(TT)对人体进行免疫会导致外周淋巴细胞对TT以及单向混合淋巴细胞反应的反应性受到抑制。在免疫后3天或7天采集的细胞中观察到最强的抑制作用。这些反应性在第14天重新出现,并在免疫后第21天达到初始水平。通过分别培养免疫后第7天采集的纯化T淋巴细胞或B淋巴细胞来研究各种细胞类型的作用。单独的B细胞不会被TT或同种异体细胞刺激。纯化的T细胞比初始的总细胞群体受到的刺激要多得多。当B细胞与T细胞混合培养时,会出现对刺激的抑制作用,使3H-胸腺嘧啶核苷掺入量降低到初始群体的水平。用5-溴脱氧尿苷处理后,再用TT刺激的细胞暴露于光线下,会消除它们对随后TT刺激的反应能力;而处理过的细胞对同种异体淋巴细胞的反应性没有受到显著影响,反之亦然。这些结果表明,每种刺激物都激活了一个单独的T细胞群体,但体内免疫引发了特异性和非特异性抑制活性的发展。很可能这种抑制活性是由贴壁的、带有表面免疫球蛋白的(B)细胞产生的。

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