کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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3216085 | 1203556 | 2010 | 8 صفحه PDF | دانلود رایگان |

The β2 integrins are important for both transendothelial migration of leukocytes and T-cell activation during antigen presentation. In T cells, triggering of leukocyte functional antigen-1 (LFA-1) is required for full activation and T-helper (Th)1/Th2 differentiation. We used CD18-deficient (CD18−/-) mice to examine the role of LFA-1 in the activation of T cells. Compared with wild-type controls, CD18−/- T cells proliferated normally when stimulated with antibodies against CD3 and CD28, but secreted significantly less IFN-γ and IL-2 than their wild-type counterparts. However, when T cells were stimulated with dendritic cells (DCs) that provide additional LFA-1 ligation, the proliferation of CD18−/- T cells was significantly reduced, whereas cytokine production remained impaired. The diminished proliferative capacity of CD18−/- T cells could be fully compensated for by additional triggering of the T-cell receptor, but not by additional stimulation through the costimulatory molecule, CD28. Thus, ligation of LFA-1 on T cells participates in regulation of Th1 cytokines in vivo. In addition, LFA-1 primarily exerts an effect as an enhancer of TCR signalling and does not facilitate classical costimulation.
Journal: Journal of Investigative Dermatology - Volume 130, Issue 4, April 2010, Pages 1005–1012