4.2 Article

Blood and Gastric FOXP3+ T Cells Are Not Decreased in Human Gastric Graft-versus-Host Disease

Journal

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
Volume 17, Issue 4, Pages 486-496

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bbmt.2010.09.015

Keywords

FOXP3; Regulatory T cells; Graft-versus-host disease; Hematopoietic cell transplant; Gastrointestinal; Mucosal

Funding

  1. NIH/NIDDK [1K08 DK081659, T32 DK07742]
  2. NIH/NIAID [T32 AI-007411, 1R21 AI069788-01]
  3. NIH/NCI [NIH/NCI CA15704, 18029]

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Previous studies suggest regulatory T cells (Tregs) inhibit graft-versus-host disease (GVHD) in mouse and human hematopoietic cell transplant (HCT) recipients. As the gastrointestinal tract represents one of the most common and severe sites of GVHD-related tissue damage, we sought to determine whether a deficit in circulating or gastric mucosal Treg numbers correlates with the clinical onset of gastric GVHD. We used the marker FOXP3 to quantify Tregs in blood and in gastric antral biopsies in a cohort of 60 allogeneic HCT recipients undergoing endoscopy at a single center to evaluate symptoms suspicious for gastrointestinal GVHD. We show for the first time in the gastric mucosa and, contrary to existing reports, in the blood, that the percent of T cells expressing FOXP3 is at least as high in the presence as in the absence of GVHD involving the upper gut. There was no correlation of Treg frequency with the histologic or clinical severity of gastrointestinal GVHD. We conclude that Treg depletion is not a central feature in the pathogenesis of gastric GVHD in humans. Biol Blood Marrow Transplant 17: 486-496 (2011) (C) 2011 American Society for Blood and Marrow Transplantation

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