Fig. 4From: OX40 signaling is involved in the autoactivation of CD4+CD28− T cells and contributes to the pathogenesis of autoimmune arthritisAdoptive transfer in CIA mice. Passive CIA was induced by intravenous transfer of sorted CD4+CD28−OX40− (a, n = 4), CD4+CD28+OX40− (b, n = 4), CD4+CD28−OX40+ (c, n = 5), or CD4+CD28+OX40+ (d, n = 4) T-cell subsets. CIA mice that received transfers with CD4+CD28−OX40− and CD4+CD28−OX40+ T cells had aggravated arthritis development compared with control CIA mice (n = 4). CD4+CD28+OX40− and CD4+CD28+OX40+ T cells did not significantly affect arthritis development compared with control CIA mice. The arthritis scores of different groups of recipient mice are shown as the mean ± SD. e H&E histological stains (×200 original magnification) and micro-computed tomographic analysis of representative ankle sections from the experiments shown in a, b, c, and d. CIA Collagen-induced arthritis, H&E Hematoxylin and eosinBack to article page