Peyer's patches: organizing B-cell responses at the intestinal frontier

被引:268
作者
Reboldi, Andrea [1 ,2 ]
Cyster, Jason G. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Howard Hughes Med Inst, 513 Parnassus Ave, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Microbiol & Immunol, 513 Parnassus Ave, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
B cells; dendritic cells; antibodies; cell trafficking; repertoire development; mucosa; FOLLICLE-ASSOCIATED EPITHELIUM; CLASS SWITCH RECOMBINATION; IMMUNOGLOBULIN-A GENERATION; MUCOSAL IGA RESPONSES; INNATE LYMPHOID-CELLS; DENDRITIC CELLS; GUT IGA; ORAL IMMUNIZATION; IMMUNE-RESPONSE; LAMINA PROPRIA;
D O I
10.1111/imr.12400
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
Secondary lymphoid tissues share the important function of bringing together antigens and rare antigen-specific lymphocytes to foster induction of adaptive immune responses. Peyer's patches (PPs) are unique compared to other secondary lymphoid tissues in their continual exposure to an enormous diversity of microbiome- and food-derived antigens and in the types of pathogens they encounter. Antigens are delivered to PPs by specialized microfold (M) epithelial cells and they may be captured and presented by resident dendritic cells (DCs). In accord with their state of chronic microbial antigen exposure, PPs exhibit continual germinal center (GC) activity. These GCs not only contribute to the generation of B cells and plasma cells producing somatically mutated gut antigen-specific IgA antibodies but have also been suggested to support non-specific antigen diversification of the B-cell repertoire. Here, we review current understanding of how PPs foster B-cell encounters with antigen, how they favor isotype switching to the secretory IgA isotype, and how their GC responses may uniquely contribute to mucosal immunity.
引用
收藏
页码:230 / 245
页数:16
相关论文
共 173 条
[1]
Follicular dendritic cell networks of primary follicles and germinal centers: Phenotype and function [J].
Allen, Christopher D. C. ;
Cyster, Jason G. .
SEMINARS IN IMMUNOLOGY, 2008, 20 (01) :14-25
[2]
Appearance and phenotype of murine follicular dendritic cells expressing VCAM-1 [J].
Balogh, P ;
Aydar, Y ;
Tew, JG ;
Szakal, AK .
ANATOMICAL RECORD, 2002, 268 (02) :160-168
[3]
Identification and distribution of developing innate lymphoid cells in the fetal mouse intestine [J].
Bando, Jennifer K. ;
Liang, Hong-Erh ;
Locksley, Richard M. .
NATURE IMMUNOLOGY, 2015, 16 (02) :153-+
[4]
Germinal Center Centroblasts Transition to a Centrocyte Phenotype According to a Timed Program and Depend on the Dark Zone for Effective Selection [J].
Bannard, Oliver ;
Horton, Robert M. ;
Allen, Christopher D. C. ;
An, Jinping ;
Nagasawa, Takashi ;
Cyster, Jason G. .
IMMUNITY, 2013, 39 (05) :912-924
[5]
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
[6]
Somatic hypermutation in the absence of DNA-dependent protein kinase catalytic subunit (DNA-PKcs) or recombination-activating gene (RAG)1 activity [J].
Bemark, M ;
Sale, JE ;
Kim, HJ ;
Berek, C ;
Cosgrove, RA ;
Neuberger, MS .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (10) :1509-1514
[7]
Induction of gut IgA production through T cell-dependent and T cell-independent pathways [J].
Bemark, Mats ;
Boysen, Preben ;
Lycke, Nils Y. .
YEAR IN IMMUNOLOGY, 2012, 1247 :97-116
[8]
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
[9]
Re-utilization of germinal centers in multiple Peyer's patches results in highly synchronized, oligoclonal, and affinity-matured gut IgA responses [J].
Bergqvist, P. ;
Stensson, A. ;
Hazanov, L. ;
Holmberg, A. ;
Mattsson, J. ;
Mehr, R. ;
Bemark, M. ;
Lycke, N. Y. .
MUCOSAL IMMUNOLOGY, 2013, 6 (01) :122-135
[10]
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