Perez V L, Lederer J A, Lichtman A H, Abbas A K
Department of Pathology, Brigham & Women's Hospital, Boston, MA 02115, USA.
Int Immunol. 1995 May;7(5):869-75. doi: 10.1093/intimm/7.5.869.
Using an in vitro model for the development of IFN-gamma-producing (Th1) and IL-4-producing (Th2) cells from CD4+ T lymphocytes expressing a transgenic TCR, we show that IL-12 and IL-4 are the most potent stimuli for the differentiation of naive T cells to effector populations. When combinations of cytokines are present during T cell priming, the effect of IL-4 is dominant. Furthermore, differentiated Th1 cells can be converted into IL-4 producers by exposure to IL-4, but the Th2 phenotype is not reversible. The stability of Th2 populations may limit the ability to regulate Th2-dominant responses in pathologic situations.
利用一种体外模型,从表达转基因TCR的CD4 + T淋巴细胞中培养产生γ干扰素的(Th1)细胞和产生白细胞介素-4的(Th2)细胞,我们发现白细胞介素-12和白细胞介素-4是将初始T细胞分化为效应细胞群体的最有效刺激物。当在T细胞致敏过程中存在细胞因子组合时,白细胞介素-4的作用占主导。此外,分化的Th1细胞通过暴露于白细胞介素-4可转化为产生白细胞介素-4的细胞,但Th2表型不可逆转。Th2群体的稳定性可能会限制在病理情况下调节以Th2为主的反应的能力。