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Publication : αβ TCR⁺ T cells, but not B cells, promote autoimmune keratitis in b10 mice lacking γδ T cells.

First Author  O'Brien RL Year  2012
Journal  Invest Ophthalmol Vis Sci Volume  53
Issue  1 Pages  301-8
PubMed ID  22199243 Mgi Jnum  J:191499
Mgi Id  MGI:5461980 Doi  10.1167/iovs.11-8855
Citation  O'Brien RL, et al. (2012) alphabeta TCR(+) T cells, but not B cells, promote autoimmune keratitis in b10 mice lacking gammadelta T cells. Invest Ophthalmol Vis Sci 53(1):301-8
abstractText  PURPOSE: To investigate additional factors in the spontaneous development of keratitis previously reported in B10.TCRdelta(-)/(-) female mice. METHODS: The study tested whether susceptible B10.TCRdelta(-)/(-) mice have dry eyes compared with resistant B6.TCRdelta(-)/(-) females and also rederived the B10.TCRdelta(-)/(-) strain to test for the role of an infectious agent. Also assessed was whether adoptive transfer of alphabeta T cells from autoimmune mice induced keratitis in resistant mice. In addition, a potential role was examined for B cells or autoantibodies by B-cell inactivation, and the role of female hormones was tested by ovariectomy. Finally, the study investigated whether adoptive transfer of Vgamma1(+) gammadelta T cells confers protection. RESULTS: Tear production in B10.TCRdelta(-)/(-) females was actually higher than in B6.TCRdelta(-)/(-) controls. Rederived B10.TCRdelta(-)/(-) mice still developed keratitis. Keratitis was induced in resistant mice after adoptive transfer of alphabeta T cells from keratitic donors. Inactivation of B cells from susceptible mice had no effect on the development of keratitis. Ovariectomy did not significantly reduce disease in B10.TCRdelta(-)/(-) females. Adoptive transfer of Vgamma1(+) cells from wild-type donors reduced keratitis in B10.TCRdelta(-)/(-) females. CONCLUSIONS: Neither low tear levels nor ovarian hormones contribute to spontaneous keratitis in B10.TCRdelta(-)/(-) female mice, nor does it appear to depend on an infectious agent carried vertically in this strain. However, alphabeta T cells from keratitic hosts are sufficient to induce disease in the resistant B10.TCRbeta(-)/(-)delta(-)/(-) strain. Autoaggressive alphabeta T cells in the absence of Vgamma1(+) T cells in B10.TCRdelta(-)/(-) mice may be insufficiently checked to prevent disease.
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