Pinchuk L M, Polacino P S, Agy M B, Klaus S J, Clark E A
Department of Microbiology, University of Washington Medical Center, Seattle 98195.
Immunity. 1994 Jul;1(4):317-25. doi: 10.1016/1074-7613(94)90083-3.
We investigated the role of blood dendritic cells (DCs) in transmission of HIV-1 from infected to uninfected CD4+ T cells, and the accessory molecules involved. DCs promoted transmission from infected to uninfected CD4+ cells, but DCs themselves were not infectable. DC-mediated transmission was blocked by MAb to CD4 and MHC class II, but strongly increased by MAb to CD40 on DCs or CD28 on T cells. The DC-dependent infection was inhibitable by anti-CD80 and a soluble fusion protein of the CD80 ligand, CTLA4; soluble CTLA4 immunoglobulin also blocked infection augmented by cross-linking CD40. These data suggest a linkage between CD40-CD40L and CD28-CD80 counterreceptors on DCs and T cells, and spread of HIV infection in vivo.
我们研究了血液树突状细胞(DCs)在HIV-1从感染的CD4+ T细胞向未感染的CD4+ T细胞传播中的作用以及相关的辅助分子。DCs促进了HIV-1从感染细胞向未感染的CD4+细胞的传播,但DCs本身不能被感染。DC介导的传播可被抗CD4和MHC II类单克隆抗体阻断,但可被DC上的抗CD40单克隆抗体或T细胞上的抗CD28单克隆抗体显著增强。抗CD80和CD80配体CTLA4的可溶性融合蛋白可抑制DC依赖性感染;可溶性CTLA4免疫球蛋白也可阻断因CD40交联而增强的感染。这些数据表明DCs和T细胞上的CD40-CD40L以及CD28-CD80共受体之间存在联系,并且提示了HIV感染在体内的传播机制。