Chang Nan-Hua, Manion Kieran P, Loh Christina, Pau Evelyn, Baglaenko Yuriy, Wither Joan E
Arthritis Centre of Excellence, Division of Genetics and Development, Krembil Research Institute, Toronto, Ontario, Canada.
Department of Immunology, University of Toronto, Toronto, Ontario, Canada.
PLoS One. 2017 Jun 19;12(6):e0179506. doi: 10.1371/journal.pone.0179506. eCollection 2017.
Lupus is characterized by a loss of B cell tolerance leading to autoantibody production. In this study, we explored the mechanisms underlying this loss of tolerance using B6 congenic mice with an interval from New Zealand Black chromosome 1 (denoted c1(96-100)) sufficient for anti-nuclear antibody production. Transgenes for soluble hen egg white lysozyme (sHEL) and anti-HEL immunoglobulin were crossed onto this background and various tolerance mechanisms examined. We found that c1(96-100) mice produced increased levels of IgM and IgG anti-HEL antibodies compared to B6 mice and had higher proportions of germinal center B cells and long-lived plasma cells, suggesting a germinal center-dependent breach of B cell anergy. Consistent with impaired anergy induction, c1(96-100) double transgenic B cells showed enhanced survival and CD86 upregulation. Hematopoietic chimeric sHEL mice with a mixture of B6 and c1(96-100) HEL transgenic B cells recapitulated these results, suggesting the presence of a B cell autonomous defect. Surprisingly, however, there was equivalent recruitment of B6 and c1(96-100) B cells into germinal centers and differentiation to splenic plasmablasts in these mice. In contrast, there were increased proportions of c1(96-100) T follicular helper cells and long-lived plasma cells as compared to their B6 counterparts, suggesting that both B and T cell defects are required to breach germinal center tolerance in this model. This possibility was further supported by experiments showing an enhanced breach of anergy in double transgenic mice with a longer chromosome 1 interval with additional T cell defects.
狼疮的特征是B细胞耐受性丧失,导致自身抗体产生。在本研究中,我们使用携带来自新西兰黑鼠1号染色体的一段间隔(标记为c1(96 - 100))的B6同源基因小鼠来探究这种耐受性丧失的潜在机制,该间隔足以产生抗核抗体。将可溶性鸡卵清溶菌酶(sHEL)和抗HEL免疫球蛋白的转基因导入该背景,并检测各种耐受机制。我们发现,与B6小鼠相比,c1(96 - 100)小鼠产生的IgM和IgG抗HEL抗体水平升高,生发中心B细胞和长寿浆细胞的比例更高,这表明生发中心依赖性地打破了B细胞无反应性。与无反应性诱导受损一致,c1(96 - 100)双转基因B细胞显示出增强的存活能力和CD86上调。具有B6和c1(96 - 100) HEL转基因B细胞混合物的造血嵌合sHEL小鼠重现了这些结果,表明存在B细胞自主性缺陷。然而,令人惊讶的是,在这些小鼠中,B6和c1(96 - 100) B细胞向生发中心的募集以及向脾母细胞的分化是相当的。相比之下,与B6对应细胞相比,c1(96 - 100) T滤泡辅助细胞和长寿浆细胞的比例增加,这表明在该模型中,打破生发中心耐受性需要B细胞和T细胞缺陷。用更长的1号染色体间隔且具有额外T细胞缺陷的双转基因小鼠进行的实验进一步支持了这种可能性,即无反应性的打破增强。