Salomon B, Bluestone J A
Department of Pathology, Ben May Institute for Cancer Research, University of Chicago, IL 60637, USA.
J Immunol. 1998 Nov 15;161(10):5138-42.
The role of CD28/B7 and LFA-1/ICAM costimulation in proliferation and Th1/Th2 differentiation of naive CD4+ T cells was addressed using T cells from DO11.10 TCR transgenic mice stimulated by dendritic cells. The blockade of either CD28/B7 or LFA-1/ICAM interactions partially inhibited T cell proliferation. By comparison, blocking CD28/B7 costimulation inhibited IL-4 and IL-5 (Th2 cytokine) production, whereas blocking LFA-1/ICAM-1 or LFA-1/ICAM-2 led to a significant increase (15- to 40-fold) of Th2 cytokines. The combination of anti-ICAM-1 and anti-ICAM-2 mAbs had a synergistic effect with a 100- to 1000-fold increase of Th2 cytokine production. Thus, these two costimulatory pathways have opposing roles in the regulation of Th2 development.
利用来自DO11.10 TCR转基因小鼠的T细胞,通过树突状细胞刺激,研究了CD28/B7和LFA-1/ICAM共刺激在初始CD4 + T细胞增殖及Th1/Th2分化中的作用。阻断CD28/B7或LFA-1/ICAM相互作用均可部分抑制T细胞增殖。相比之下,阻断CD28/B7共刺激可抑制IL-4和IL-5(Th2细胞因子)的产生,而阻断LFA-1/ICAM-1或LFA-1/ICAM-2则导致Th2细胞因子显著增加(15至40倍)。抗ICAM-1和抗ICAM-2单克隆抗体的联合使用具有协同效应,Th2细胞因子产生增加100至1000倍。因此,这两条共刺激途径在Th2发育的调节中具有相反的作用。