The bilateral responsiveness between intestinal microbes and IgA

被引:148
作者
Macpherson, Andrew J. [1 ]
Koeller, Yasmin [1 ]
Mccoy, Kathy D. [1 ]
机构
[1] Univ Bern, Maurice Muller Labs DKF, Univ Klin Viszerale Chirurg & Med Inselspital, CH-3010 Bern, Switzerland
关键词
IgA; commensal microbiota; germinal centres; somatic hypermutation; follicular helper T cells; follicular regulatory T cells; follicular dendritic cells; Peyer's patch; isolated lymphoid follicles; SEGMENTED FILAMENTOUS BACTERIA; MUCOSAL IMMUNE-SYSTEM; CLASS SWITCH RECOMBINATION; IMMUNOGLOBULIN-A; PEYERS-PATCHES; PLASMA-CELLS; MONONUCLEAR-CELLS; GUT MICROBIOTA; SECRETORY IGA; T(H)17 CELLS;
D O I
10.1016/j.it.2015.06.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The immune system has developed strategies to maintain a homeostatic relationship with the resident microbiota. IgA is central in holding this relationship, as the most dominant immunoglobulin isotype at the mucosal surface of the intestine. Recent studies report a role for IgA in shaping the composition of the intestinal microbiota and exploit strategies to characterise IgA-binding bacteria for their inflammatory potential. We review these findings here, and place them in context of the current understanding of the range of microorganisms that contribute to the IgA repertoire and the pathways that determine the quality of the IgA response. We examine why only certain intestinal microbes are coated with IgA, and discuss how understanding the determinants of this specific responsiveness may provide insight into diseases associated with dysbiosis.
引用
收藏
页码:460 / 470
页数:11
相关论文
共 79 条
[1]
IgA-Producing Plasma Cells Originate From Germinal Centers That Are Induced by B-Cell Receptor Engagement in Humans [J].
Barone, Francesca ;
Vossenkamper, Anna ;
Boursier, Laurent ;
Su, Wen ;
Watson, Alan ;
John, Susan ;
Dunn-Walters, Deborah K. ;
Fields, Paul ;
Wijetilleka, Sonali ;
Edgeworth, Jonathan D. ;
Spencer, Jo .
GASTROENTEROLOGY, 2011, 140 (03) :947-956
[2]
BEATTY DW, 1983, J CLIN LAB IMMUNOL, V12, P31
[3]
SERUM AND SMALL INTESTINAL IMMUNOGLOBULIN LEVELS IN UNDERNOURISHED CHILDREN [J].
BELL, RG ;
TURNER, KJ ;
GRACEY, M ;
SUHARJONO ;
SUNOTO .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1976, 29 (04) :392-397
[4]
The majority of intestinal IgA+ and IgG+ plasmablasts in the human gut are antigen-specific [J].
Benckert, Julia ;
Schmolka, Nina ;
Kreschel, Cornelia ;
Zoller, Markus Josef ;
Sturm, Andreas ;
Wiedenmann, Bertram ;
Wardemann, Hedda .
JOURNAL OF CLINICAL INVESTIGATION, 2011, 121 (05) :1946-1955
[5]
BENVENIS.J, 1971, J IMMUNOL, V107, P1647
[6]
BENVENISTE J, 1971, J IMMUNOL, V107, P1656
[7]
Gut IgA class switch recombination in the absence of CD40 does not occur in the lamina propria and is independent of germinal centers [J].
Bergqvist, Peter ;
Gardby, Eva ;
Stensson, Anneli ;
Bemark, Mats ;
Lycke, Nils Y. .
JOURNAL OF IMMUNOLOGY, 2006, 177 (11) :7772-7783
[8]
T Cell-Independent IgA Class Switch Recombination Is Restricted to the GALT and Occurs Prior to Manifest Germinal Center Formation [J].
Bergqvist, Peter ;
Stensson, Anneli ;
Lycke, Nils Y. ;
Bemark, Mats .
JOURNAL OF IMMUNOLOGY, 2010, 184 (07) :3545-3553
[9]
The Mucosal Immune System and Its Integration with the Mammary Glands [J].
Brandtzaeg, Per .
JOURNAL OF PEDIATRICS, 2010, 156 (02) :S8-S15
[10]
B cell receptor signal strength determines B cell fate [J].
Casola, S ;
Otipoby, KL ;
Alimzhanov, M ;
Humme, S ;
Uyttersprot, N ;
Kutok, JL ;
Carroll, MC ;
Rajewsky, K .
NATURE IMMUNOLOGY, 2004, 5 (03) :317-327