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ADCC 介导的非中和抗体可在 HIV-1 感染早期发挥免疫压力作用。

ADCC-mediating non-neutralizing antibodies can exert immune pressure in early HIV-1 infection.

机构信息

Department of Surgery, Duke University, Durham, North Carolina, United States of America.

Institute of Infectious Diseases and Molecular Medicine and Division of Medical Virology, University of Cape Town, Cape Town, South Africa.

出版信息

PLoS Pathog. 2021 Nov 17;17(11):e1010046. doi: 10.1371/journal.ppat.1010046. eCollection 2021 Nov.

DOI:10.1371/journal.ppat.1010046
PMID:34788337
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8598021/
Abstract

Despite antibody-dependent cellular cytotoxicity (ADCC) responses being implicated in protection from HIV-1 infection, there is limited evidence that they control virus replication. The high mutability of HIV-1 enables the virus to rapidly adapt, and thus evidence of viral escape is a very sensitive approach to demonstrate the importance of this response. To enable us to deconvolute ADCC escape from neutralizing antibody (nAb) escape, we identified individuals soon after infection with detectable ADCC responses, but no nAb responses. We evaluated the kinetics of ADCC and nAb responses, and viral escape, in five recently HIV-1-infected individuals. In one individual we detected viruses that escaped from ADCC responses but were sensitive to nAbs. In the remaining four participants, we did not find evidence of viral evolution exclusively associated with ADCC-mediating non-neutralizing Abs (nnAbs). However, in all individuals escape from nAbs was rapid, occurred at very low titers, and in three of five cases we found evidence of viral escape before detectable nAb responses. These data show that ADCC-mediating nnAbs can drive immune escape in early infection, but that nAbs were far more effective. This suggests that if ADCC responses have a protective role, their impact is limited after systemic virus dissemination.

摘要

尽管抗体依赖性细胞细胞毒性(ADCC)反应被认为与预防 HIV-1 感染有关,但仅有有限的证据表明它们可以控制病毒复制。HIV-1 的高度突变性使其能够迅速适应,因此病毒逃避的证据是证明这种反应重要性的非常敏感的方法。为了能够从中和抗体(nAb)逃避中推断出 ADCC 逃避,我们在感染后不久就发现了具有可检测的 ADCC 反应但没有 nAb 反应的个体。我们评估了五名新近感染 HIV-1 的个体的 ADCC 和 nAb 反应以及病毒逃避的动力学。在一名个体中,我们检测到逃避 ADCC 反应但对 nAbs 敏感的病毒。在其余四名参与者中,我们没有发现与 ADCC 介导的非中和抗体(nnAbs)相关的病毒进化的证据。然而,在所有个体中,nAbs 的逃避非常迅速,发生在非常低的滴度下,在五种情况中的三种情况下,我们在可检测到 nAb 反应之前发现了病毒逃避的证据。这些数据表明,ADCC 介导的 nnAbs 可以在早期感染中引发免疫逃避,但 nAbs 更为有效。这表明如果 ADCC 反应具有保护作用,那么它们在系统性病毒传播后的影响是有限的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623a/8598021/02558c7a6b70/ppat.1010046.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623a/8598021/ca89b5b5a712/ppat.1010046.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623a/8598021/e2742c77d099/ppat.1010046.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623a/8598021/e44fe611916b/ppat.1010046.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623a/8598021/6fda43f3a16d/ppat.1010046.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623a/8598021/0b75bf59e556/ppat.1010046.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623a/8598021/62d861365cea/ppat.1010046.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623a/8598021/02558c7a6b70/ppat.1010046.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623a/8598021/ca89b5b5a712/ppat.1010046.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623a/8598021/e2742c77d099/ppat.1010046.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623a/8598021/e44fe611916b/ppat.1010046.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623a/8598021/6fda43f3a16d/ppat.1010046.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623a/8598021/0b75bf59e556/ppat.1010046.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623a/8598021/62d861365cea/ppat.1010046.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623a/8598021/02558c7a6b70/ppat.1010046.g007.jpg

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