Intestinal plasma cells predominantly produce immunoglobulin (Ig) A, however, their functionaldiversity remains poorly characterized. Here we show that murine intestinal IgA plasmacells can be newly classified into two populations on the basis of CD11b expression, whichcannot be discriminated by currently known criteria such as general plasma cell markers, B cellorigin and T cell dependence. CD11b+ IgA+ plasma cells require the lymphoid structure ofPeyer’s patches, produce more IgA than CD11b+ IgA+ plasma cells, proliferate vigorously,and require microbial stimulation and IL-10 for their development and maintenance. Thesefeatures allow CD11b+ IgA+ plasma cells to mediate early-phase antigen-specific intestinalIgA responses induced by oral immunization with protein antigen. These findings reveal thefunctional diversity of IgA+ plasma cells in the murine intestine.
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机译:肠浆细胞主要产生免疫球蛋白(Ig)A,但是,其功能多样性仍然很差。在这里,我们显示可以基于CD11b表达将鼠肠道IgA浆细胞新分为两类,不能通过目前已知的标准(例如一般浆细胞标记物,B细胞起源和T细胞依赖性)来区分。 CD11b + IgA +浆细胞需要Peyer贴片的淋巴样结构,比CD11b + IgA +浆细胞产生更多的IgA,旺盛增殖,并且需要微生物刺激和IL-10来发育和维持。这些功能允许CD11b + IgA +浆细胞介导通过蛋白抗原口服免疫诱导的早期抗原特异性肠道IgA反应。这些发现揭示了鼠肠中IgA +浆细胞的功能多样性。
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