首页> 外文期刊>The journal of immunology >Staphylococcal Protein A Deletes B-1a and Marginal Zone B Lymphocytes Expressing Human Immunoglobulins: An Immune Evasion Mechanism
【24h】

Staphylococcal Protein A Deletes B-1a and Marginal Zone B Lymphocytes Expressing Human Immunoglobulins: An Immune Evasion Mechanism

机译:葡萄球菌蛋白A删除表达人类免疫球蛋白的B-1a和边缘B区淋巴细胞:一种免疫逃逸机制

获取原文
           

摘要

Protein A (SpA) of Staphylococcus aureus is endowed with the capacity to interact with the H chain variable region (VH) of human Abs and to target 40% of B lymphocytes. To investigate whether this property represents a virulence factor and to determine the in vivo consequences of the confrontation of SpA with B lymphocytes, we used transgenic mice expressing fully human Abs. We found that administration of soluble SpA reduces B-1a lymphocytes of the peritoneal cavity and marginal zone B lymphocytes of the spleen, resulting in a markedly deficient type 2 humoral response. Single-cell PCR analysis and sequencing of the Ab VH gene repertoire revealed a significant reduction of VH3+ marginal zone B cells. Since the two B lymphocyte subsets targeted are involved in innate immune functions, our data suggest that crippling of humoral immunity by S. aureus represents an immune evasion mechanism that may aggravate recurrent infections.
机译:金黄色葡萄球菌的蛋白A(SpA)具有与人类Abs的H链可变区(VH)相互作用并靶向B淋巴细胞> 40%的能力。为了研究这种特性是否代表一种毒力因子并确定SpA与B淋巴细胞对抗的体内后果,我们使用了表达完全人类Abs的转基因小鼠。我们发现,施用可溶性SpA可以减少腹膜腔的B-1a淋巴细胞和脾脏的边缘B区淋巴细胞,从而导致2型体液反应明显不足。 Ab VH基因库的单细胞PCR分析和测序表明VH3 +边缘区B细胞明显减少。由于靶向的两个B淋巴细胞亚群都参与先天免疫功能,因此我们的数据表明,金黄色葡萄球菌对体液免疫的削弱代表了一种免疫逃逸机制,可能加剧复发性感染。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号