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Cell-Cell Transmission Enables HIV-1 to Evade Inhibition by Potent CD4bs Directed Antibodies

机译:细胞之间的传递使HIV-1能够通过有效的CD4bs定向抗体逃避抑制作用

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摘要

HIV is known to spread efficiently both in a cell-free state and from cell to cell, however the relative importance of the cell-cell transmission mode in natural infection has not yet been resolved. Likewise to what extent cell-cell transmission is vulnerable to inhibition by neutralizing antibodies and entry inhibitors remains to be determined. Here we report on neutralizing antibody activity during cell-cell transmission using specifically tailored experimental strategies which enable unambiguous discrimination between the two transmission routes. We demonstrate that the activity of neutralizing monoclonal antibodies (mAbs) and entry inhibitors during cell-cell transmission varies depending on their mode of action. While gp41 directed agents remain active, CD4 binding site (CD4bs) directed inhibitors, including the potent neutralizing mAb VRC01, dramatically lose potency during cell-cell transmission. This implies that CD4bs mAbs act preferentially through blocking free virus transmission, while still allowing HIV to spread through cell-cell contacts. Thus providing a plausible explanation for how HIV maintains infectivity and rapidly escapes potent and broadly active CD4bs directed antibody responses in vivo.
机译:众所周知,HIV可以在无细胞状态和从一个细胞到另一个细胞有效地传播,但是,细胞-细胞传播方式在自然感染中的相对重要性尚未得到解决。同样,细胞间的传播在多大程度上容易受到中和抗体和进入抑制剂的抑制作用尚待确定。在这里,我们报告了使用专门定制的实验策略在细胞间传输过程中中和抗体活性的方法,该策略能够明确区分两种传输途径。我们证明中和单克隆抗体(mAbs)和进入抑制剂在细胞间传输过程中的活性取决于其作用方式。尽管gp41指导的药物保持活性,但CD4结合位点(CD4bs)指导的抑制剂(包括有效的中和mAb VRC01)在细胞间传递过程中显着丧失了效力。这意味着CD4bs mAb通过阻止自由病毒传播而优先发挥作用,同时仍允许HIV通过细胞与细胞的接触传播。因此,对于HIV如何在体内保持感染力并迅速逃脱有针对性和广泛活性的CD4bs定向抗体反应提供了合理的解释。

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