Gerosa F, Paganin C, Peritt D, Paiola F, Scupoli M T, Aste-Amezaga M, Frank I, Trinchieri G
Immunology and Infectious Disease Institute, University of Verona, Italy.
J Exp Med. 1996 Jun 1;183(6):2559-69. doi: 10.1084/jem.183.6.2559.
Interleukin-12 (IL-12) induces differentiation of T helper 1 (Th1) cells, primarily through its ability to prime T cells for high interferon-gamma (IFN-gamma) production. We now report that the presence of IL-12 during the first several days of in vitro clonal expansion in limiting dilution cultures of polyclonally stimulated human peripheral blood CD4+ and CD8+ T cells also induces stable priming for high IL-10 production. This effect was demonstrated with T cells from both healthy donors and HIV+ patients. Priming for IL-4 production, which requires IL-4, was maximum in cultures containing both IL-12 and IL-4. IL-4 modestly inhibited the IL-12-induced priming for IFN-gamma, but almost completely suppressed the priming for IL-10 production. A proportion of the clones generated from memory CD45RO+ cells, but not those generated from naive CD45RO- CD4+ T cells, produced some combinations of IFN-gamma, IL-10, and IL-4 even in the absence of IL-12 and IL-4, suggesting in vivo cytokine priming; virtually all CD4+ clones generated from either CD45RO(-) or (+) cells, however, produced high levels of both IFN-gamma and IL-10 when IL-12 was present during expansion. These results indicate that each Th1-type (IFN-gamma) and Th2-type (IL-4 and IL-10) cytokine gene is independently regulated in human T cells and that the dichotomy between T cells with the cytokine production pattern of Th1 and Th2 cells is not due to a direct differentiation-inducing effect of immunoregulatory cytokines, but rather to secondary selective mechanisms. Particular combinations of cytokines induce a predominant generation of T cell clones with anomalous patterns of cytokine production (e.g., IFN-gamma and IL-4 or IFN-gamma and IL-10) that can also be found in a proportion of fresh peripheral blood T cells with "memory" phenotype or clones generated from them and that may identify novel Th subsets with immunoregulatory functions.
白细胞介素-12(IL-12)主要通过促使T细胞大量产生干扰素-γ(IFN-γ)的能力来诱导辅助性T细胞1(Th1)分化。我们现在报告,在多克隆刺激的人外周血CD4+和CD8+ T细胞的有限稀释培养物中,体外克隆扩增的最初几天存在IL-12,也会诱导稳定的大量产生IL-10的启动。健康供体和HIV+患者的T细胞都证实了这种效应。需要IL-4才能产生IL-4的启动,在同时含有IL-12和IL-4的培养物中达到最大值。IL-4适度抑制IL-12诱导的IFN-γ启动,但几乎完全抑制IL-10产生的启动。从记忆性CD45RO+细胞产生的一部分克隆,而不是从初始CD45RO-CD4+ T细胞产生的克隆,即使在没有IL-12和IL-4的情况下也会产生IFN-γ、IL-10和IL-4的某些组合,提示体内细胞因子启动;然而,当扩增过程中存在IL-12时,从CD45RO(-)或(+)细胞产生的几乎所有CD4+克隆都会大量产生IFN-γ和IL-10。这些结果表明,在人T细胞中,每个Th1型(IFN-γ)和Th2型(IL-4和IL-10)细胞因子基因都是独立调节的,并且具有Th1和Th2细胞细胞因子产生模式的T细胞之间的二分法不是由于免疫调节细胞因子的直接分化诱导作用,而是由于二级选择机制。特定的细胞因子组合会诱导产生具有异常细胞因子产生模式(如IFN-γ和IL-4或IFN-γ和IL-10)的T细胞克隆占优势,这种模式也可以在一部分具有“记忆”表型的新鲜外周血T细胞或从它们产生的克隆中发现,并且可能识别出具有免疫调节功能的新型Th亚群。