| Literature DB >> 27562257 |
Shinsaku Okai1, Fumihito Usui1, Shuhei Yokota1, Yusaku Hori-I1, Makoto Hasegawa2, Toshinobu Nakamura3, Manabu Kurosawa4, Seiji Okada5, Kazuya Yamamoto6, Eri Nishiyama6, Hiroshi Mori6, Takuji Yamada6, Ken Kurokawa7, Satoshi Matsumoto8, Masanobu Nanno8, Tomoaki Naito8, Yohei Watanabe8, Tamotsu Kato9, Eiji Miyauchi9, Hiroshi Ohno9,10,11, Reiko Shinkura1,12.
Abstract
Immunoglobulin A (IgA) is the main antibody isotype secreted into the intestinal lumen. IgA plays a critical role in the defence against pathogens and in the maintenance of intestinal homeostasis. However, how secreted IgA regulates gut microbiota is not completely understood. In this study, we isolated monoclonal IgA antibodies from the small intestine of healthy mouse. As a candidate for an efficient gut microbiota modulator, we selected a W27 IgA, which binds to multiple bacteria, but not beneficial ones such as Lactobacillus casei. W27 could suppress the cell growth of Escherichia coli but not L. casei in vitro, indicating an ability to improve the intestinal environment. Indeed W27 oral treatment could modulate gut microbiota composition and have a therapeutic effect on both lymphoproliferative disease and colitis models in mice. Thus, W27 IgA oral treatment is a potential remedy for inflammatory bowel disease, acting through restoration of host-microbial symbiosis.Entities:
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Year: 2016 PMID: 27562257 DOI: 10.1038/nmicrobiol.2016.103
Source DB: PubMed Journal: Nat Microbiol ISSN: 2058-5276 Impact factor: 17.745