Wen L, Barber D F, Pao W, Wong F S, Owen M J, Hayday A
Department of Biology, Yale University, New Haven, CT 06511, USA.
J Immunol. 1998 Feb 15;160(4):1965-74.
The division of CD4+ alpha beta T cells into Th1 and Th2 subsets has become an established and important paradigm. The respective activities of these subsets appear to have profound effects on the course of infectious and autoimmune diseases. It is believed that specific programs of differentiation induce the commitment of an uncommitted Th0 precursor cell to Th1 or Th2. A component of these programs is hypothesized to be the nature of MHC-peptide antigen presentation to the alpha beta T cell. It has heretofore remained uncertain whether a Th1/Th2 classification likewise defines, at the clonal level, gamma delta T cells. Such cells do not, as a general rule, express either CD4 or CD8 alpha beta, and they do not commonly recognize peptide-MHC. In this report, gamma delta cell clones are described that conform strikingly to the Th1/Th2 classification, both by cytokine expression and by functional activities of the clones in vitro and in vivo. Provocatively, both the gamma delta cell clones and primary gamma delta cells in vivo showed a strong association of the Th2 phenotype with CD4 expression. These results are discussed with regard to the immunoregulatory role that is increasingly emerging for gamma delta cells.
CD4+αβT细胞分化为Th1和Th2亚群已成为一个既定且重要的范例。这些亚群各自的活性似乎对感染性疾病和自身免疫性疾病的病程有着深远影响。据信,特定的分化程序会促使未分化的Th0前体细胞分化为Th1或Th2。这些程序的一个组成部分被推测为MHC-肽抗原呈递给αβT细胞的性质。迄今为止,Th1/Th2分类在克隆水平上是否同样适用于γδT细胞仍不确定。一般来说,这类细胞既不表达CD4也不表达CD8αβ,它们通常也不识别肽-MHC。在本报告中,描述了γδ细胞克隆,这些克隆在细胞因子表达以及体外和体内克隆的功能活性方面都与Th1/Th2分类惊人地相符。令人惊讶的是,γδ细胞克隆和体内的原代γδ细胞均显示Th2表型与CD4表达之间存在强关联。针对γδ细胞日益凸显的免疫调节作用对这些结果进行了讨论。