Brombacher F, Köhler G, Eibel H
Max-Planck-Institut für Immunobiologie, Freiburg, Germany.
J Exp Med. 1991 Dec 1;174(6):1335-46. doi: 10.1084/jem.174.6.1335.
To analyze in vivo the induction of B cell tolerance against a T cell surface antigen, we generated transgenic mice expressing an anti-CD8.2 mu heavy chain gene. We show that self-specific B cells are efficiently tolerized if they express the membrane-bound form of the transgenic mu chain on their surface but that they can escape tolerization if they express only the secreted form. In the latter, we find an enhanced expression of anti-CD8.2 antibodies after polyclonal B cell activation. As a result, transgenic anti-CD8.2 antibodies bind to the CD8+ T cells but they did not induce their elimination. Furthermore, we observed the preferential expression of a limited subset of endogenous light chains with the transgenic mu chain. This suggests a positive or negative selection for particular heavy and light chain combinations in B lymphocytes.
为了在体内分析针对T细胞表面抗原的B细胞耐受性的诱导情况,我们构建了表达抗CD8.2μ重链基因的转基因小鼠。我们发现,如果自身特异性B细胞在其表面表达转基因μ链的膜结合形式,它们会被有效地耐受,但如果它们仅表达分泌形式,则可以逃避耐受。在后者中,我们发现多克隆B细胞激活后抗CD8.2抗体的表达增强。结果,转基因抗CD8.2抗体与CD8 + T细胞结合,但并未诱导其清除。此外,我们观察到内源性轻链的有限子集与转基因μ链的优先表达。这表明B淋巴细胞中特定重链和轻链组合存在阳性或阴性选择。