Chang T L, Shea C M, Urioste S, Thompson R C, Boom W H, Abbas A K
Combined Program in Pediatric Gastroenterology and Nutrition, Massachusetts General Hospital, Boston 02114.
J Immunol. 1990 Nov 1;145(9):2803-8.
Murine CD4+ T cell clones have been classified into at least two subsets, Th1 and Th2, on the basis of their distinct lymphokine secretion profiles and functions. In the present study, we compared the functional responses of Th1 and Th2 clones to Ag presentation by splenic B cells and peritoneal macrophages. Th2 clones secreted IL-4 in response to Ag presented by resting B cells, but their optimal proliferation required the addition of IL-1 or a source of IL-1. The degree of IL-1 dependence varied among the four Th2 clones examined. In contrast, Th1 clones secreted IL-2 and proliferated in response to Ag presented by both B cells and macrophages, without any requirement for exogenous IL-1. Furthermore, the proliferation of Th2 clones in response to Ag presented by splenocytes or macrophages was inhibited by an IL-1R antagonist. These results indicate that IL-1 is an important costimulator for the expansion of the Th2 subset of CD4+ T cells. The different requirements for the proliferation of Th1 and Th2 cells may be responsible for the preferential expansion of one or the other subset under different conditions of immunization.
根据不同的淋巴因子分泌谱和功能,小鼠CD4+ T细胞克隆已被分为至少两个亚群,即Th1和Th2。在本研究中,我们比较了Th1和Th2克隆对脾B细胞和腹腔巨噬细胞提呈抗原的功能反应。Th2克隆在静息B细胞提呈抗原时分泌IL-4,但其最佳增殖需要添加IL-1或IL-1来源。在所检测的四个Th2克隆中,IL-1依赖性程度各不相同。相比之下,Th1克隆分泌IL-2,并在B细胞和巨噬细胞提呈抗原时增殖,无需外源性IL-1。此外,IL-1R拮抗剂可抑制Th2克隆对脾细胞或巨噬细胞提呈抗原的增殖反应。这些结果表明,IL-1是CD4+ T细胞Th2亚群扩增的重要共刺激因子。Th1和Th2细胞增殖的不同需求可能是在不同免疫条件下其中一个或另一个亚群优先扩增的原因。