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对OKT4+和OKT8+人类T细胞亚群内功能异质性的进一步剖析。

Further dissection of the functional heterogeneity within the OKT4+ and OKT8+ human T cell subsets.

作者信息

Thomas Y, Rogozinski L, Rothman P, Rabbani L E, Andrews S, Irigoyen O H, Chess L

出版信息

J Clin Immunol. 1982 Jul;2(3 Suppl):8S-14S.

PMID:6215426
Abstract

Previous studies have suggested functional heterogeneity within the OKT4+ and the OKT8+ populations. For example, after activation the OKT4+ population contains not only helper cells but also cells capable of suppressing B cell differentiation. Previous studies also indicate that the reciprocal T cell population, OKT8+, does not provide helper activity but contains cytotoxic effector cells and radiosensitive cells important in the suppression of B cell differentiation. Using a new differentiation antigen, OKT17, which recognizes a surface antigen present on the majority of resting normal peripheral T lymphocytes but is present only on a subset of OKT4+ cells after activation, evidence was obtained that two functionally mature subsets can be distinguished within the OKT4+ population itself: OKT4+17+ radiosensitive suppressor cells and OKT4+17- radiosensitive helper cells. Recently, another monoclonal antibody, OKT20, has been described which is present on a small percentage of resting lymphocytes but is expressed in varying proportions on activated T cells. Functional analysis of normal resting human T lymphocytes demonstrated that the OKT20-depleted T cell subset was able to generate cytotoxic cells and to suppress antibody production to the same extent as did OKT8+ cells. On the other hand, when unselected T lymphocytes were cultured for six days in a mixed lymphocyte reaction and then depleted of OKT20 reactive cells, the cytotoxic effector T cells were eliminated. In contrast, OKT20-depleted T cells after identical activation were still able to suppress antibody production. These data provide evidence that following activation of OKT8+ cells, the OKT20 differentiation antigen becomes selectively expressed on cytotoxic effectors but not on suppressor cells.

摘要

先前的研究表明,OKT4+和OKT8+群体内存在功能异质性。例如,激活后,OKT4+群体不仅包含辅助细胞,还包含能够抑制B细胞分化的细胞。先前的研究还表明,与之对应的T细胞群体OKT8+不提供辅助活性,但包含细胞毒性效应细胞和对抑制B细胞分化很重要的放射敏感性细胞。使用一种新的分化抗原OKT17,它识别大多数静止正常外周T淋巴细胞上存在的表面抗原,但激活后仅存在于OKT4+细胞的一个亚群上,由此获得的证据表明,在OKT4+群体本身内可以区分出两个功能成熟的亚群:OKT4+17+放射敏感性抑制细胞和OKT4+17-放射敏感性辅助细胞。最近,又描述了另一种单克隆抗体OKT20,它存在于一小部分静止淋巴细胞上,但在活化T细胞上以不同比例表达。对正常静止人T淋巴细胞的功能分析表明,去除OKT20的T细胞亚群能够产生细胞毒性细胞,并能在与OKT8+细胞相同的程度上抑制抗体产生。另一方面,当未选择的T淋巴细胞在混合淋巴细胞反应中培养六天,然后去除OKT20反应性细胞时,细胞毒性效应T细胞被消除。相反,相同激活后去除OKT20的T细胞仍然能够抑制抗体产生。这些数据提供了证据,表明在OKT8+细胞激活后,OKT20分化抗原在细胞毒性效应细胞上选择性表达,而在抑制细胞上不表达。

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