Previous studies in our laboratory have shown that human intestinal mucosal T cells have little expression of the Leu-8 antigen which is normally found on the majority of peripheral blood T cells. In addition, CD4+, Leu-8+ T cells were shown to directly suppress immunoglobulin (Ig) synthesis, whereas CD4+, Leu-8 negative T cells provide help for immunoglobulin synthesis. It was also shown that modulation of the Leu-8 antigen with monoclonal anti-Leu-8 antibody enhances the suppressor function of CD4 T cells. To further examine the functional significance of decreased expression of the Leu-8 antigen on intestinal mucosal T cells, in the present study we compared the helper and suppressor function of lamina propria lymphocytes. At high T/B cell ratios, it was found that intestinal T cells provided more help for Ig synthesis than peripheral T cells. Whereas pretreatment of peripheral blood cells with anti-Leu-8 under crosslinking conditions significantly inhibited Ig synthesis, pretreatment of intestinal lymphocytes did not. In further studies of the mechanism of this phenomenon, CD4 T cells were isolated and tested for suppressor function following treatment with anti-Leu- 8; it was found that peripheral blood, but not lamina propria CD4 T cells suppressed Ig synthesis. When highly purified populations of CD4+, Leu-8 negative and CD4+, Leu-8+ T cells were prepared from peripheral blood and intestinal lamina propria, it was found that the peripheral blood and intestinal T cell subpopulations had similar helper and suppressor function, respectively. Thus, the diminished suppressor function of intestinal CD4 T cells is due to the diminished number of CD4, Leu-8+ T cells in the lamina propria rather than any intrinsic difference in their function. This difference in T cell function in the intestine may be important for immunoglobulin production in the mucosa and in the understanding of intestinal inflammation in IBD.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Intramural Research (Z01)
Project #
1Z01AI000354-06
Application #
3822046
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
6
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Niaid Extramural Activities
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Meng, Guangxun; Zhang, Fuping; Fuss, Ivan et al. (2009) A mutation in the Nlrp3 gene causing inflammasome hyperactivation potentiates Th17 cell-dominant immune responses. Immunity 30:860-74
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Strober, Warren; Murray, Peter J; Kitani, Atsushi et al. (2006) Signalling pathways and molecular interactions of NOD1 and NOD2. Nat Rev Immunol 6:9-20
Strober, Warren (2006) Immunology. Unraveling gut inflammation. Science 313:1052-4

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