Zhang Jingwu
Health Science Center, Shanghai Institutes of Biological Sciences and Shanghai Second Medical University, China.
Cell Mol Immunol. 2004 Oct;1(5):321-7.
Immunization with inactivated autoreactive T cells (T cell vaccination) selected from individual's own T cell repertoire provides a unique in vivo setting for testing immune regulation that is known to involve interactions of a variety of related surface molecules (1). It induces regulatory immune responses that closely resemble the in vivo situation where the immune system is challenged by clonal activation and expansion of given T cell populations in various autoimmune diseases. T cell vaccination provides a powerful means of eliciting natural reactions of the immune system in response to clonal expansion of T cells, which can be used as a therapeutic approach to suppress or eliminate specific pathogenic autoreactive T cells in autoimmune conditions. Clinical trials using T cell vaccination to deplete autoreactive T cells in human autoimmune conditions have begun to reveal the pathologic relevance of various autoimmune T cell populations in the disease processes, providing a unique opportunity to test the autoimmune theories in a clinical setting.
用从个体自身T细胞库中挑选出的灭活自身反应性T细胞进行免疫接种(T细胞疫苗接种),为测试免疫调节提供了一种独特的体内环境,已知这种调节涉及多种相关表面分子的相互作用(1)。它诱导的调节性免疫反应与体内情况非常相似,在各种自身免疫性疾病中,免疫系统会受到特定T细胞群体的克隆激活和扩增的挑战。T细胞疫苗接种提供了一种强大的手段来引发免疫系统对T细胞克隆扩增的自然反应,这可以用作一种治疗方法,在自身免疫性疾病中抑制或消除特定的致病性自身反应性T细胞。使用T细胞疫苗接种来清除人类自身免疫性疾病中自身反应性T细胞的临床试验,已开始揭示各种自身免疫性T细胞群体在疾病过程中的病理相关性,为在临床环境中测试自身免疫理论提供了独特的机会。