4.7 Article

The intestinal chemokine thymus-expressed chemokine (CCL25) attracts IgA antibody-secreting cells

Journal

JOURNAL OF EXPERIMENTAL MEDICINE
Volume 195, Issue 2, Pages 269-275

Publisher

ROCKEFELLER UNIV PRESS
DOI: 10.1084/jem.20010670

Keywords

homing; migration; chemokine; B cell; isotype

Funding

  1. NIAID NIH HHS [5 T32 AI07290, R01 AI047822, R21 AI047822, T32 AI007290, 5R37AI121362-16, AI37832, R37 AI047822, AI47822] Funding Source: Medline
  2. NIDDK NIH HHS [F32 DK010022, DK10022] Funding Source: Medline
  3. NIGMS NIH HHS [R01 GM037734, R37 GM037734, GM37734] Funding Source: Medline

Ask authors/readers for more resources

Immunoglobulin A (IgA) provides protection against pathogens at mucosal surfaces. Chemotactic responses have been hypothesized to target IgA plasma cells involved in mucosal immune responses. We show here that thymus-expressed chemokine (TECK, CCL25) is a potent and selective chemoattractant for IgA antibody-secreting cells (ASC), efficiently recruiting IgA-producing cells front spleen, Peyer's patches, and mesenteric lymph node. Cells secreting IgA antibody in response to rotavirus, an intestinal pathogen, also respond well. In contrast. IgG- and IgM-ASC respond poorly. Epithelial cells in the small intestines, a principal site of IgA-ASC localization and IgA production in the body, highly and selectively express TECK. The migration of IgA-ASC to the intestinal epithelial cell chemokine TECK may help target IgA-producing cells to the gut wall, thus helping define and segregate the intestinal immune response.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available