Huang Ching-Tai, Huso David L, Lu Zhenbing, Wang Tianhong, Zhou Gang, Kennedy Eugene P, Drake Charles G, Morgan David J, Sherman Linda A, Higgins Amy D, Pardoll Drew M, Adler Adam J
Oncology Center and Division of Comparative Medicine, Johns Hopkins Medical Institutions, Baltimore, MD 21231, USA.
J Immunol. 2003 Apr 15;170(8):3945-53. doi: 10.4049/jimmunol.170.8.3945.
An important process in the generation of tolerance to peripheral self-Ags is the induction of unresponsiveness in mature specific T cells. Although the end stage of this process, termed anergy, is well defined, the pathway by which naive T cells become anergic remains to be elucidated. Using an in vivo self-tolerance model, we demonstrate that CD4(+) T cells pass through a significant effector stage on their way to an anergic state. This stage is characterized by production of effector cytokines, provision of help for CD8(+) T cells, and induction of in vivo pathology within organs that express cognate Ag. These results suggest that the initial activation stage in T cell tolerance is similar to that seen in memory induction. They also suggest that autoimmune pathology can result during the natural process of tolerance induction rather than requiring that tolerance be broken.
对外周自身抗原产生耐受的一个重要过程是诱导成熟的特异性T细胞无反应性。尽管这个过程的终末阶段,即无反应性,已得到明确界定,但初始T细胞变成无反应性的途径仍有待阐明。利用一个体内自身耐受模型,我们证明CD4(+) T细胞在进入无反应性状态的过程中会经历一个显著的效应阶段。这个阶段的特征是效应细胞因子的产生、为CD8(+) T细胞提供帮助以及在表达同源抗原的器官内诱导体内病理变化。这些结果表明,T细胞耐受中的初始激活阶段与记忆诱导中的相似。它们还表明,自身免疫性病理变化可在耐受诱导的自然过程中产生,而不是需要耐受被打破。