Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 104, Issue 40, Pages 15823-15828Publisher
NATL ACAD SCIENCES
DOI: 10.1073/pnas.0707421104
Keywords
immunoregulation; phagocytosis; apoptotic; dendritic cell; regulatory T cell
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Funding
- Medical Research Council [G9900991B] Funding Source: researchfish
- NCI NIH HHS [U54-CA112967, U54 CA112967] Funding Source: Medline
- Wellcome Trust [064487] Funding Source: Medline
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The gastrointestinal tract is constantly challenged by foreign antigens and commensal bacteria but nonetheless is able to maintain a state of immunological quiescence. Recent advances have highlighted the importance of active suppression by regulatory lymphocytes and immunosuppressive cytokines in controlling mucosal immunity. Failures of these mechanisms contribute to the development of inflammatory bowel disease, but how these regulatory networks are established remains unclear. Here, we demonstrate key roles for alpha v integrins in regulation of mucosal immunity. We report that deletion of av in the immune system causes severe colitis, autoimmunity, and cancer. Mice lacking immune cell av have fewer regulatory T (Treg) cells in the colon and corresponding increases in activated T cells and T cell cytokine production, leading to colitis. Using conditional gene targeting, we demonstrate that this is specifically attributable to loss of av from myeloid cells. Furthermore, we show that gut-associated macrophages and dendritic cells fail both to remove apoptotic cells efficiently and to induce Treg cells. Our results identify a vital role for myeloid av integrins in generating mucosal Treg cells and emphasize the importance of antigen-presenting cells in establishing immune tolerance.
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