Powers G D, Miller R A
Department of Pathology, Boston University School of Medicine, MA 02118.
J Immunol. 1987 Oct 15;139(8):2567-72.
T lymphocytes are thought to provide "help" for B cells by activating them from the resting state, by secretion of antigen-nonspecific lymphokines that promote B cell differentiation and maturation, and by providing signals that induce isotype switching. To clarify the extent to which these different forms of helper activity could be carried out by individual T cells, we set up cultures in which B cells activated, and were in turn themselves stimulated by, limiting numbers of T cells through differences at the H-2 or Mls loci. At T cell doses at which responses were likely to represent the activity of individual helper T cells (or their immediate clonal progeny), we found that some T cells were able both to produce interleukin 2 (IL-2) and to induce secretion of both IgM and IgG, whereas others induced immunoglobulin (Ig) secretion without detectable IL-2 production, and still others made IL-2 but did not promote antibody secretion. We could not detect B cell stimulatory factor 1 production by alloantigen-stimulated T cells, and the addition of antibodies to B cell stimulatory factor 1 did not prevent Ig production. Two results, however--higher Ig accumulation in those wells that received an IL-2-producing cell, and inhibition by anti-IL-2 receptor antibodies of B cell but not T cell function--are consistent with a direct stimulatory effect of IL-2 on B cells in this system. The pattern of helper functions exhibited by T cells freshly isolated from mice differs from that inferred from studies of cloned lines of T cells in long term cultures.
T淋巴细胞被认为通过以下方式为B细胞提供“帮助”:将B细胞从静止状态激活,分泌促进B细胞分化和成熟的抗原非特异性淋巴因子,以及提供诱导同种型转换的信号。为了阐明这些不同形式的辅助活性在多大程度上可由单个T细胞执行,我们建立了培养体系,其中B细胞被激活,并且反过来又通过H-2或Mls位点的差异受到有限数量T细胞的刺激。在T细胞剂量下,其反应可能代表单个辅助性T细胞(或其直接克隆后代)的活性,我们发现一些T细胞既能产生白细胞介素2(IL-2),又能诱导IgM和IgG的分泌,而其他一些T细胞则诱导免疫球蛋白(Ig)分泌但未检测到IL-2的产生,还有一些T细胞产生IL-2但不促进抗体分泌。我们未检测到同种异体抗原刺激的T细胞产生B细胞刺激因子1,并且添加针对B细胞刺激因子1的抗体并不能阻止Ig的产生。然而,有两个结果——在接受产生IL-2细胞的孔中Ig积累更高,以及抗IL-2受体抗体抑制B细胞而非T细胞功能——与IL-2在该系统中对B细胞的直接刺激作用一致。从小鼠新鲜分离的T细胞所表现出的辅助功能模式与从长期培养的T细胞克隆系研究中推断出的模式不同。