IgG transport across mucosal barriers by neonatal Fc receptor for IgG and mucosal immunity.

Springer seminars in immunopathology Pub Date : 2006-12-01 Epub Date: 2006-10-19 DOI:10.1007/s00281-006-0054-z
Masaru Yoshida, Atsuhiro Masuda, Timothy T Kuo, Kanna Kobayashi, Steven M Claypool, Tetsuya Takagawa, Hiromu Kutsumi, Takeshi Azuma, Wayne I Lencer, Richard S Blumberg
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引用次数: 68

Abstract

Mucosal secretions of the human gastrointestinal, respiratory, and genital tracts contain significant quantities of IgG. The neonatal Fc receptor for IgG (FcRn) plays a major role in regulating host IgG levels and transporting IgG and associated antigens across polarized epithelial barriers. The FcRn can then recycle the IgG/antigen complex back across the intestinal barrier into the lamina propria for processing by dendritic cells and presentation to CD4(+) T cells in regional organized lymphoid structures. FcRn, through its ability to secrete and absorb IgG, thus integrates luminal antigen encounters with systemic immune compartments and, as such, provides essential host defense and immunoregulatory functions at the mucosal surfaces.

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新生儿Fc受体对IgG和粘膜免疫的影响。
人类胃肠道、呼吸道和生殖道的粘膜分泌物中含有大量的IgG。新生儿IgG Fc受体(FcRn)在调节宿主IgG水平和转运IgG及相关抗原跨越极化上皮屏障中起主要作用。然后,FcRn可以回收IgG/抗原复合物,穿过肠屏障进入固有层,由树突状细胞处理,并呈递给区域组织淋巴结构中的CD4(+) T细胞。FcRn通过其分泌和吸收IgG的能力,将腔内抗原遭遇与全身免疫区室整合,从而在粘膜表面提供必要的宿主防御和免疫调节功能。
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