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T细胞表面糖蛋白的生物学功能。

Biological functions of T-cell surface glycoproteins.

作者信息

Thomas Y, Lederman S, Rogozinski L, Chess L

出版信息

Diagn Immunol. 1983;1(3):100-3.

PMID:6238748
Abstract

The OKT4 monoclonal antibody reacts with a 62 KD cell surface glycoprotein present on a subset of human T cells with the capacity to help or induce B-cell differentiation. The OKT8 monoclonal antibody reacts with a 76 KD cell surface glycoprotein present on a subset of human T cells with the capacity to suppress B-cell differentiation. The current studies were undertaken to determine whether the T4 and/or T8 antigens themselves play any role in the helper or suppressor function mediated by OKT4+ or OKT8+ cells. Specifically, we asked if monoclonal antibodies that react with noncompeting epitopes on the T4 or T8 molecules could block helper or suppressor function. Isolated human B cells were triggered in vitro to differentiate into antibody-forming cells (AFC) by autologous OKT4+ cells and macrophages in the presence or absence of OKT4 antibodies. By means of a reverse hemolytic plaque assay, AFC were detected as plaque-forming cells (PFC). We found that OKT4A, but not OKT4, antibody inhibited the PFC response over a wide range of concentrations. The antibodies OKT4B, OKT4C, OKT4D, OKT4E inhibited the PFC response to varying degrees. Importantly, inhibition by OKT4A occurred only if the antibody was present during the first 24 hours of cell culture. In the second set of experiments, OKT8+ cells were added to cultures containing B cells, and OKT4+ cells in the presence or absence of OKT8 antibodies, PFC activity was measured 7 days later. We found that the addition of OKT8E or OKT8G, but not OKT8B, OKT8C, OKT8D, OKT8F, or OKT8H, antibodies significantly inhibits the suppressor function mediated by OKT8+ cells.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

OKT4单克隆抗体与一种62KD的细胞表面糖蛋白发生反应,该糖蛋白存在于一部分具有辅助或诱导B细胞分化能力的人T细胞上。OKT8单克隆抗体与一种76KD的细胞表面糖蛋白发生反应,该糖蛋白存在于一部分具有抑制B细胞分化能力的人T细胞上。进行当前这些研究是为了确定T4和/或T8抗原自身是否在由OKT4+或OKT8+细胞介导的辅助或抑制功能中发挥任何作用。具体而言,我们询问与T4或T8分子上非竞争性表位发生反应的单克隆抗体是否能够阻断辅助或抑制功能。在存在或不存在OKT4抗体的情况下,分离出的人B细胞在体外由自体OKT4+细胞和巨噬细胞触发分化为抗体形成细胞(AFC)。通过反向溶血空斑试验,将AFC检测为空斑形成细胞(PFC)。我们发现OKT4A抗体而非OKT4抗体在很宽的浓度范围内抑制PFC反应。OKT4B、OKT4C、OKT4D、OKT4E抗体在不同程度上抑制PFC反应。重要的是,仅当抗体在细胞培养的最初24小时内存在时,OKT4A才会产生抑制作用。在第二组实验中,将OKT8+细胞添加到含有B细胞和OKT4+细胞的培养物中,存在或不存在OKT8抗体,7天后测量PFC活性。我们发现添加OKT8E或OKT8G抗体而非OKT8B、OKT8C、OKT8D、OKT8F或OKT8H抗体可显著抑制由OKT8+细胞介导的抑制功能。(摘要截选至250词)

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