Longhi M Paula, Sivasankar Baalasubramanian, Omidvar Nader, Morgan B Paul, Gallimore Awen
Medical Biochemistry and Immunology, School of Medicine, Cardiff University, Wales, United Kingdom.
J Immunol. 2005 Dec 1;175(11):7098-102. doi: 10.4049/jimmunol.175.11.7098.
CD59 blocks formation of the membrane attack complex of complement by inhibiting binding of C9 to the C5b-8 complex. To investigate a role for CD59 in promoting T cell responses, we compared T cell activation in CD59a-deficient (Cd59a-/-) and wild-type (WT) mice after in vitro stimulation and after infection with rVV. Virus-specific CD4+ T cell responses were significantly enhanced in Cd59a-/- mice compared with WT mice. Similarly, Cd59a-/- T cells responded more vigorously to in vitro stimulation with CD3-specific Abs compared with WT mice. This effect of CD59a on T cell proliferation was found to be complement-independent. Collectively, these results demonstrate that CD59a down-modulates CD4+ T cell activity in vitro and in vivo, thereby revealing another link between complement regulators and T cell activation.
CD59通过抑制C9与C5b-8复合物的结合来阻止补体膜攻击复合物的形成。为了研究CD59在促进T细胞反应中的作用,我们比较了体外刺激后以及感染重组痘苗病毒(rVV)后CD59a缺陷型(Cd59a-/-)小鼠和野生型(WT)小鼠的T细胞活化情况。与WT小鼠相比,Cd59a-/-小鼠中病毒特异性CD4+ T细胞反应显著增强。同样,与WT小鼠相比,Cd59a-/- T细胞对CD3特异性抗体的体外刺激反应更强烈。发现CD59a对T细胞增殖的这种作用不依赖于补体。总体而言,这些结果表明CD59a在体外和体内下调CD4+ T细胞活性,从而揭示了补体调节因子与T细胞活化之间的另一个联系。