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Author Notes:

Correspondence: Dr. Neil A. Mabbott: The Roslin Institute & Royal (Dick) School of Veterinary Sciences, University of Edinburgh, Easter Bush, Midlothian EH25 9RG, United Kingdom Tel: +44 (0)131 651 9100 Fax: +44 (0)131 651 9105, neil.mabbott@roslin.ed.ac.uk

We thank Dr. Atsushi Kobayashi (Tohoku University Graduate School of Medicine, Sendai, Japan) for immunohistochemistry expertise.

The authors declare no competing financial conflict of interest.

Subjects:

Research Funding:

This work was supported by project (BB/J014672/1; BB/K021257/1) and Institute Strategic Programme Grant (BB/J0004332/1) funding from the Biotechnology and Biological Sciences Research Council.

I.R.W. was supported by grant funding from the National Institutes of Health (DK064730).

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Immunology
  • FOLLICLE-ASSOCIATED EPITHELIUM
  • ISOLATED LYMPHOID FOLLICLES
  • CD103(+) DENDRITIC CELLS
  • PATCH M-CELLS
  • FACTOR SPI-B
  • PEYERS PATCH
  • TUNNELING NANOTUBES
  • IMMUNOGLOBULIN-A
  • IMMUNE-RESPONSES
  • ORAL TOLERANCE

Microfold (M) cells: important immunosurveillance posts in the intestinal epithelium

Tools:

Journal Title:

Mucosal Immunology

Volume:

Volume 6, Number 4

Publisher:

, Pages 666-677

Type of Work:

Article | Post-print: After Peer Review

Abstract:

The transcytosis of antigens across the gut epithelium by microfold cells (M cells) is important for the induction of efficient immune responses to some mucosal antigens in Peyer's patches. Recently, substantial progress has been made in our understanding of the factors that influence the development and function of M cells. This review highlights these important advances, with particular emphasis on: the host genes which control the functional maturation of M cells; how this knowledge has led to the rapid advance in our understanding of M-cell biology in the steady state and during aging; molecules expressed on M cells which appear to be used as "immunosurveillance" receptors to sample pathogenic microorganisms in the gut; how certain pathogens appear to exploit M cells to infect the host; and finally how this knowledge has been used to specifically target antigens to M cells to attempt to improve the efficacy of mucosal vaccines. © 2013 Society for Mucosal Immunology.

Copyright information:

© 2021 Springer Nature Limited

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