4.8 Article

Regulatory CD4+ CD25+ cells reverse imbalances in the T cell pool of bone marrow transplanted TGε26 mice leading to the prevention of colitis

Journal

GUT
Volume 54, Issue 2, Pages 207-214

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/gut.2004.046953

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Background and aims: Erroneous thymic selection of developing T lymphocytes may be responsible for the expansion of self reactive T cells or may contribute to the absence of regulatory T cells important in controlling peripheral inflammatory processes. Colitis in bone marrow (BM) transplanted Tgepsilon26 mice is induced by abnormally activated T cells developing in an aberrant thymic microenvironment. We investigated the protective role of regulatory CD4(+) CD25(+) T cells in this model. Methods: BM from (C57BL/6xCBA/J) F1 mice was transplanted into specific pathogen free Tgepsilon26 mice (BMdouble right arrow Tgepsilon26). Transplanted mice received no cells (control), sorted CD4(+) CD25(+), or CD4(+) CD25(-) cells from mesenteric lymph nodes (MLN) of normal mice. MLN cell subsets were analysed using membrane markers. Cytokine secretion of MLN cells was measured using intracellular cytokine staining and cytokine secretion in anti-CD3 stimulated cell cultures. Colitis was measured by histological scores. Results: CD4(+) CD25(+) cells were reduced in the MLNs of BM double right arrow Tgepsilon26 mice. Transfer of regulatory CD4(+) CD25(+) but not of CD4(+) CD25(-) cells reduced the number of MLN CD4(+) T cells in BMdouble right arrowTgepsilon26 recipients and increased the number of MLN CD8(+) cells, thereby normalising the CD4(+)/ CD8(+) ratio. CD4(+) CD25(+) but not CD4(+) CD25(-) cell transfer into BMdouble right arrow Tgepsilon26 mice reduced the number of tumour necrosis factor alpha(+) CD4(+) cells and increased the secretion of transforming growth factor beta by MLN cells. Transfer of 36 x 10(5) CD4(+) CD25(+) cells after BM transplantation into Tgepsilon26 mice prevented colitis whereas CD4(+) CD25(-) cells had no protective effect. Conclusions: These results suggest that defective selection or induction of regulatory T cells in the abnormal thymus is responsible for the development of colitis in BMdouble right arrow Tgepsilon26 mice. Transfer of CD4+ CD25+ cells can control intestinal inflammation in BMdouble right arrow Tgepsilon26 mice by normalising the number and function of the MLN T cell pool.

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