Umetsu D T, Jabara H H, DeKruyff R H, Abbas A K, Abrams J S, Geha R S
Division of Allergy and Pulmonary Disease, Children's Hospital, Stanford, CA.
J Immunol. 1988 Jun 15;140(12):4211-6.
Analysis of mouse CD4+ inducer T cells at the clonal level has established that a dichotomy among CD4+ T cell clones exists with regard to types of lymphokines secreted. Mouse T cell clones designated Th1 have been shown to secrete IL-2 and IFN-gamma, whereas T cell clones designated Th2 have been shown to produce IL-4 but not IL-2 or IFN-gamma. To determine if such a dichotomy in the helper inducer T cell subset occurred in man, we examined a panel of human CD4+ helper/inducer T cell clones for patterns of lymphokine secretion and for functional activity. We identified human T cell clones which secrete IL-4 but not IL-2 or IFN-gamma, and which appeared to correspond to murine Th2 clones. In marked contrast to murine IL-2 secreting Th1 clones which do not produce IL-4 or IFN-gamma, we observed that some human T cell clones secrete IL-2, and IFN-gamma as well as IL-4. Southern blot analysis indicated that these multi-lymphokine-secreting clones represented the progeny of a single T cell. IL-4 secretion did not always correlated with enhanced ability to induce Ig synthesis. Although one T cell clone which secreted IL-2, IL-4, and IFN-gamma could efficiently induce Ig synthesis, another expressed potent cytolytic and growth inhibitory activity for B cells, and was ineffective or inhibitory in inducing Ig synthesis. These results indicate that although the equivalent of murine Th2 type cells appears to be present in man, the simple division of T cells into a Th1 and Th2 dichotomy may not hold true for human T cells.
在克隆水平上对小鼠CD4+诱导性T细胞的分析已经证实,CD4+T细胞克隆在分泌的淋巴因子类型方面存在二分法。已显示被指定为Th1的小鼠T细胞克隆分泌IL-2和IFN-γ,而被指定为Th2的T细胞克隆已显示产生IL-4,但不产生IL-2或IFN-γ。为了确定在人类辅助诱导性T细胞亚群中是否也存在这种二分法,我们检测了一组人类CD4+辅助/诱导性T细胞克隆的淋巴因子分泌模式和功能活性。我们鉴定出了分泌IL-4但不分泌IL-2或IFN-γ的人类T细胞克隆,这些克隆似乎与小鼠Th2克隆相对应。与不产生IL-4或IFN-γ的分泌IL-2的小鼠Th1克隆形成鲜明对比的是,我们观察到一些人类T细胞克隆分泌IL-2、IFN-γ以及IL-4。Southern印迹分析表明,这些分泌多种淋巴因子的克隆代表单个T细胞的后代。IL-4的分泌并不总是与诱导Ig合成的能力增强相关。虽然一个分泌IL-2、IL-4和IFN-γ的T细胞克隆能够有效地诱导Ig合成,但另一个克隆对B细胞表现出强大的细胞溶解和生长抑制活性,并且在诱导Ig合成方面无效或具有抑制作用。这些结果表明,尽管人类中似乎存在相当于小鼠Th2型的细胞,但将T细胞简单地分为Th1和Th2二分法可能不适用于人类T细胞。