Reciprocal regulation of IgA and the gut microbiota: a key mutualism in the intestine. (4th August 2021)

• Record Type: Journal Article
• Authors: Takeuchi, Tadashi; Ohno, Hiroshi
• Is Part Of: International immunology. Volume 33:Number 12(2021)
• Page Start: 781
• Page End: 786
• Publication Date: 2021-08-04
• Subjects: microbial metabolites -- microbial reactivity -- T-cell-dependent activation -- T-cell-independent B-cell activation; Immunology -- Periodicals; 616.079
• DOI: 10.1093/intimm/dxab049
• Languages: English
• ISSNs: 0953-8178

Abstract

Abstract: The mammalian intestine is home to trillions of microbes, and their colonization contributes to host physiology through the production of indispensable metabolites and competition against pathogens. However, it is also important to balance this symbiotic relationship, as overgrowth and translocation of microbes could trigger a fatal infection. IgA is the major immunoglobulin class produced and secreted in the intestine and is considered to play a pivotal role in maintaining homeostasis. In this review, we summarize recent studies exploring the interactions between IgA and the gut microbiota and explain how different types of IgA could coexist to regulate the gut microbiota. In particular, we discuss two important aspects of IgA in controlling the gut microbes: function and specificity. Differences in these two aspects appear attributable to how IgA is induced and are associated with the functions of IgA as well. Together, our review delineates a recent understanding of IgA–microbiome interactions and proposes a future direction to clarify its complexity.