Hsieh C S, Macatonia S E, Tripp C S, Wolf S F, O'Garra A, Murphy K M
Department of Pathology, Washington University School of Medicine, St. Louis, MO 63110.
Science. 1993 Apr 23;260(5107):547-9. doi: 10.1126/science.8097338.
Development of the appropriate CD4+ T helper (TH) subset during an immune response is important for disease resolution. With the use of naïve, ovalbumin-specific alpha beta T cell receptor transgenic T cell, it was found that heat-killed Listeria monocytogenes induced TH1 development in vitro through macrophage production of interleukin-12 (IL-12). Moreover, inhibition of macrophage production of IL-12 may explain the ability of IL-10 to suppress TH1 development. Murine immune responses to L. monocytogenes in vivo are of the appropriate TH1 phenotype. Therefore, this regulatory pathway may have evolved to enable innate immune cells, through interactions with microbial pathogens, to direct development of specific immunity toward the appropriate TH phenotype.
免疫应答过程中合适的CD4 +辅助性T细胞(TH)亚群的发育对于疾病的消退很重要。利用幼稚的、卵清蛋白特异性αβT细胞受体转基因T细胞,发现热灭活的单核细胞增生李斯特菌通过巨噬细胞产生白细胞介素-12(IL-12)在体外诱导TH1发育。此外,抑制巨噬细胞产生IL-12可能解释了IL-10抑制TH1发育的能力。小鼠体内对单核细胞增生李斯特菌的免疫应答具有合适的TH1表型。因此,这种调节途径可能已经进化,以使先天免疫细胞能够通过与微生物病原体的相互作用,将特异性免疫的发育导向合适的TH表型。