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CD11c+ T-bet+ Memory B cells: Immune Maintenance during Chronic Infection and Inflammation?

机译:CD11c + T-bet +记忆B细胞:慢性感染和炎症期间的免疫维持吗?

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摘要

CD11c+ T-bet+ B cells have now been detected and characterized in different experimental and clinical settings, in both mice and humans. Whether such cells are monolithic, or define subsets of B cells with different functions is not yet known. Our studies have identified CD11c+ IgM+ CD19hi splenic IgM memory B cells that appear at approximately three weeks post-ehrlichial infection, and persist indefinitely, during low-level chronic ehrlichial infection. Although the CD11c+T-bet+ B cells we have described are distinct, they appear to share many features with similar cells detected under diverse conditions, including viral infections, aging, and autoimmunity. We propose that CD11c+ T-bet+ B cells as a group share characteristics of memory B cells that are maintained under conditions of inflammation and/or low-level chronic antigen stimulation. In some cases, these cells may be advantageous, by providing immunity to re-infection, but in others may be deleterious, by contributing to aged-associated autoimmune responses.
机译:现在已经在小鼠和人类的不同实验和临床环境中检测到CD11c + T-bet + B细胞并对其进行了表征。这样的单元是整体的还是定义具有不同功能的B单元的子集尚不清楚。我们的研究确定了CD11c + IgM + CD19 脾脏IgM记忆B细胞出现在埃希氏菌感染后大约三周,并在低水平慢性埃希氏菌感染期间无限期存在。尽管我们描述的CD11c + T-bet + B细胞是截然不同的,但它们似乎与在各种条件下检测到的相似细胞具有许多特征,包括病毒感染,衰老和自身免疫。我们建议CD11c + T-bet + B细胞作为一个组共享在炎症和/或低水平的慢性抗原刺激条件下维持的记忆B细胞的特征。在某些情况下,这些细胞通过提供对再感染的免疫力可能是有利的,而在另一些情况下,通过促进衰老相关的自身免疫反应可能是有害的。

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