Ward T, Powell R M, Pipkin P A, Evans D J, Minor P D, Almond J W
School of Animal and Microbial Sciences, University of Reading, Whiteknights, Reading RG6 6AJ, United Kingdom.
J Virol. 1998 Jul;72(7):5360-5. doi: 10.1128/JVI.72.7.5360-5365.1998.
A monoclonal antibody (MAb) that blocks most echoviruses (EVs) from infecting rhabdomyosarcoma (RD) cells has been isolated. By using the CELICS cloning method (T. Ward, P. A. Pipkin, N. A. Clarkson, D. M. Stone, P. D. Minor, and J. W. Almond, EMBO J. 13:5070-5074, 1994), the ligand for this antibody has been identified as beta2-microglobulin (beta2m), the 12-kDa protein that associates with class I heavy chains to form class I HLA complexes. A commercial MAb (MAb 1350) against beta2m was also found to block EV7 infection without affecting binding to its receptor, DAF, or replication of EV7 viral RNA inside cells. Entry of EV7 into cells was reduced by only 30% by antibody and cytochalasin D, an inhibitor of endocytosis mediated by caveolae and clathrin-coated pits, but was not significantly reduced by sodium azide. The block to virus entry by cytochalasin D was additive to the block induced by antibody. We suggest that EV7 rapidly enters into a multicomponent receptor complex prior to entry into cells and that this initial entry event requires beta2m or class I HLA for infection to proceed.
已分离出一种可阻止大多数肠道病毒(EVs)感染横纹肌肉瘤(RD)细胞的单克隆抗体(MAb)。通过使用CELICS克隆方法(T. Ward、P. A. Pipkin、N. A. Clarkson、D. M. Stone、P. D. Minor和J. W. Almond,《欧洲分子生物学组织杂志》13:5070 - 5074,1994年),已确定该抗体的配体为β2-微球蛋白(β2m),即与I类重链结合形成I类HLA复合物的12 kDa蛋白。还发现一种针对β2m的商业单克隆抗体(单克隆抗体1350)可阻止EV7感染,且不影响其与受体衰变加速因子(DAF)的结合或细胞内EV7病毒RNA的复制。抗体和细胞松弛素D(一种由小窝和网格蛋白包被小窝介导的内吞作用抑制剂)使EV7进入细胞的能力仅降低30%,但叠氮化钠未使其显著降低。细胞松弛素D对病毒进入的阻断作用与抗体诱导的阻断作用具有累加性。我们认为,EV7在进入细胞之前迅速进入多组分受体复合物,且这种初始进入事件需要β2m或I类HLA才能继续感染。