Schmidt K N, Cyster J G
Department of Microbiology and Immunology, University of California, San Francisco 94143, USA.
J Immunol. 1999 Jan 1;162(1):284-91.
In mice with a diverse B cell repertoire, hen egg lysozyme (HEL) autoantigen-binding B cells are excluded from follicles and eliminated in 3 days. To explore the roles of competitor B cells and of T cells in this mechanism of self-tolerance, HEL-specific B cells were transferred into mice containing HEL and deficient in endogenous B cells (muMT), T cells (TCR-/-), or B and T cells (RAG1-/-). Previous studies suggested a dual requirement for B cell receptor (BCR) engagement and competition in HEL autoantigen-binding B cell elimination, but interpretation of these experiments has been confounded by the possible failure to independently regulate autoantigen concentration and competitor B cell frequency. In experiments in this study, we have fixed one variable, HEL concentration, while varying the second, the presence or absence of other B cells. By this approach, we find that follicular exclusion and rapid elimination of autoreactive B cells require BCR engagement plus competition with other B cells, rather than BCR engagement alone. We also find, by transfers into T cell-deficient mice, that T cells are not required for this peripheral tolerance mechanism. Unexpectedly, in mice lacking both T cells and competitor B cells (RAG1-/-), transferred HEL-binding cells survive less well than in mice just lacking competitor B cells. These results suggest T cells can enhance autoreactive B cell survival. Enhanced survival of autoreactive B cells, due to the presence of T cells and the lack of competitor B cells, might contribute to the elevated frequency of autoimmunity in B cell-deficient individuals.
在具有多样化B细胞库的小鼠中,卵清溶菌酶(HEL)自身抗原结合B细胞被排除在滤泡之外,并在3天内被清除。为了探究竞争B细胞和T细胞在这种自身耐受机制中的作用,将HEL特异性B细胞转入含有HEL且内源性B细胞(muMT)、T细胞(TCR-/-)或B细胞和T细胞(RAG1-/-)缺陷的小鼠体内。先前的研究表明,在HEL自身抗原结合B细胞清除过程中,B细胞受体(BCR)的参与和竞争是双重必需的,但这些实验的解释因可能无法独立调节自身抗原浓度和竞争B细胞频率而受到混淆。在本研究的实验中,我们固定了一个变量,即HEL浓度,同时改变另一个变量,即其他B细胞的存在与否。通过这种方法,我们发现滤泡排除和自身反应性B细胞的快速清除需要BCR的参与以及与其他B细胞的竞争,而不仅仅是BCR的参与。我们还通过转入T细胞缺陷小鼠发现,这种外周耐受机制不需要T细胞。出乎意料的是,在缺乏T细胞和竞争B细胞的小鼠(RAG1-/-)中,转入的HEL结合细胞的存活情况比仅缺乏竞争B细胞的小鼠更差。这些结果表明T细胞可以增强自身反应性B细胞的存活。由于T细胞的存在和竞争B细胞的缺乏,自身反应性B细胞存活的增强可能导致B细胞缺陷个体自身免疫频率的升高。