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Human gut-associated lymphoid tissues (GALT); diversity, structure, and function

Mörbe, Urs M LU ; Jørgensen, Peter B ; Fenton, Thomas M ; von Burg, Nicole ; Riis, Lene B ; Spencer, Jo and Agace, William W LU (2021) In Mucosal Immunology
Abstract

Gut-associated lymphoid tissues (GALT) are the key antigen sampling and adaptive immune inductive sites within the intestinal wall. Human GALT includes the multi-follicular Peyer's patches of the ileum, the vermiform appendix, and the numerous isolated lymphoid follicles (ILF) which are distributed along the length of the intestine. Our current understanding of GALT diversity and function derives primarily from studies in mice, and the relevance of many of these findings to human GALT remains unclear. Here we review our current understanding of human GALT diversity, structure, and composition as well as their potential for regulating intestinal immune responses during homeostasis and inflammatory bowel disease (IBD). Finally, we outline... (More)

Gut-associated lymphoid tissues (GALT) are the key antigen sampling and adaptive immune inductive sites within the intestinal wall. Human GALT includes the multi-follicular Peyer's patches of the ileum, the vermiform appendix, and the numerous isolated lymphoid follicles (ILF) which are distributed along the length of the intestine. Our current understanding of GALT diversity and function derives primarily from studies in mice, and the relevance of many of these findings to human GALT remains unclear. Here we review our current understanding of human GALT diversity, structure, and composition as well as their potential for regulating intestinal immune responses during homeostasis and inflammatory bowel disease (IBD). Finally, we outline some key remaining questions regarding human GALT, the answers to which will advance our understanding of intestinal immune responses and provide potential opportunities to improve the treatment of intestinal diseases.

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author
; ; ; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Mucosal Immunology
publisher
Nature Publishing Group
external identifiers
  • scopus:85103200580
  • pmid:33753873
ISSN
1933-0219
DOI
10.1038/s41385-021-00389-4
language
English
LU publication?
yes
additional info
These authors contributed equally: Urs M. Mörbe, Peter B. Jørgensen, Thomas M. Fenton
id
e333dfd3-add6-4b42-8f4f-79fb27880b46
date added to LUP
2021-03-26 09:47:17
date last changed
2024-05-05 03:26:00
@article{e333dfd3-add6-4b42-8f4f-79fb27880b46,
  abstract     = {{<p>Gut-associated lymphoid tissues (GALT) are the key antigen sampling and adaptive immune inductive sites within the intestinal wall. Human GALT includes the multi-follicular Peyer's patches of the ileum, the vermiform appendix, and the numerous isolated lymphoid follicles (ILF) which are distributed along the length of the intestine. Our current understanding of GALT diversity and function derives primarily from studies in mice, and the relevance of many of these findings to human GALT remains unclear. Here we review our current understanding of human GALT diversity, structure, and composition as well as their potential for regulating intestinal immune responses during homeostasis and inflammatory bowel disease (IBD). Finally, we outline some key remaining questions regarding human GALT, the answers to which will advance our understanding of intestinal immune responses and provide potential opportunities to improve the treatment of intestinal diseases.</p>}},
  author       = {{Mörbe, Urs M and Jørgensen, Peter B and Fenton, Thomas M and von Burg, Nicole and Riis, Lene B and Spencer, Jo and Agace, William W}},
  issn         = {{1933-0219}},
  language     = {{eng}},
  month        = {{03}},
  publisher    = {{Nature Publishing Group}},
  series       = {{Mucosal Immunology}},
  title        = {{Human gut-associated lymphoid tissues (GALT); diversity, structure, and function}},
  url          = {{http://dx.doi.org/10.1038/s41385-021-00389-4}},
  doi          = {{10.1038/s41385-021-00389-4}},
  year         = {{2021}},
}