Yamashita N, Bullington R, Clement L T
Department of Microbiology and Immunology, UCLA School of Medicine 90024.
J Clin Immunol. 1990 Sep;10(5):237-46. doi: 10.1007/BF00916699.
Cells comprising the CD4+ T-cell population are heterogeneous with regard to function, maturation, and the expression of membrane molecules such as the CD45RA antigen. Previous analyses of the CD4+ subsets defined by CD45RA antigen expression have shown that the ability to provide help for antibody production is restricted to cells within the CD4+CD45RA- subset. In the present studies, we have examined the ability of "naive" CD4+CD45RA+ cells and "memory" CD4+CD45RA- cells to provide help for the generation of alloreactive CD8+ cytotoxic T lymphocytes. When purified CD4+CD45RA+ or CD4+CD45RA- cells were cultured with autologous CD8+ cells and allogeneic E- stimulator cells, both subsets were consistently able to provide help for CD8+ cytotoxic T-cell development. In contrast, the ability to provide help for antibody production was restricted to cells in the CD4+CD45RA- subset. Differences in the mechanisms of the helper functions for these two systems were also identified. Whereas exogenous interleukin-2 (IL-2) could replace the help provided by either CD4+ subset for cytotoxic T-cell generation, IL-2 had only minimal effects on immunoglobulin production. Thus, our studies highlight the contrasting cellular requirements and mechanisms involved in "help" for B-cell differentiation versus cytotoxic T-lymphocyte generation, and they show that the helper/inducer functions of human CD4+ cells are not mediated solely by the CD4+CD45RA- subset.
构成CD4+ T细胞群体的细胞在功能、成熟度以及膜分子如CD45RA抗原的表达方面具有异质性。先前对由CD45RA抗原表达所定义的CD4+亚群的分析表明,为抗体产生提供辅助的能力仅限于CD4+CD45RA-亚群内的细胞。在本研究中,我们检测了“初始”CD4+CD45RA+细胞和“记忆”CD4+CD45RA-细胞为同种异体反应性CD8+细胞毒性T淋巴细胞的产生提供辅助的能力。当将纯化的CD4+CD45RA+或CD4+CD45RA-细胞与自体CD8+细胞和同种异体E刺激细胞一起培养时,两个亚群均始终能够为CD8+细胞毒性T细胞的发育提供辅助。相比之下,为抗体产生提供辅助的能力仅限于CD4+CD45RA-亚群中的细胞。还确定了这两个系统辅助功能机制的差异。外源性白细胞介素-2(IL-2)可以替代任一CD4+亚群为细胞毒性T细胞产生所提供的辅助,但IL-2对免疫球蛋白产生的影响极小。因此,我们的研究突出了B细胞分化与细胞毒性T淋巴细胞产生的“辅助”过程中不同的细胞需求和机制,并且表明人CD4+细胞的辅助/诱导功能并非仅由CD4+CD45RA-亚群介导。