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HIV-1 母婴变异体对广泛中和抗体表现出相似的敏感性,但敏感性因亚型而异。

HIV-1 maternal and infant variants show similar sensitivity to broadly neutralizing antibodies, but sensitivity varies by subtype.

机构信息

Division of Human Biology and Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.

出版信息

AIDS. 2013 Jun 19;27(10):1535-44. doi: 10.1097/QAD.0b013e32835faba5.

DOI:10.1097/QAD.0b013e32835faba5
PMID:23856624
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4080909/
Abstract

RATIONALE

To protect against HIV infection, passively transferred and/or vaccine-elicited neutralizing antibodies (NAbs) need to effectively target diverse subtypes that are transmitted globally. These variants are a limited subset of those present during chronic infection and display some unique features. In the case of mother-to-child transmission (MTCT), transmitted variants tend to be resistant to neutralization by maternal autologous NAbs.

METHOD

To investigate whether variants transmitted during MTCT are generally resistant to HIV-1-specific NAbs, 107 maternal or infant variants representing the dominant HIV-1 subtypes were tested against six recently identified HIV-1-specific broadly neutralizing monoclonal antibodies (bNAbs), NIH45-46W, VRC01, PGT128, PGT121, PG9 and PGT145.

RESULTS

Infant and maternal variants did not differ in their neutralization sensitivity to individual bNAbs, nor did viruses from transmitting versus nontransmitting mothers, although there was a trend for viruses from transmitting mothers to be less sensitive overall. No single bNAb neutralized all viruses, but a combination of bNAbs that target distinct epitopes covered 100% of the variants tested. Compared with heterosexually transmitted variants, vertically transmitted variants were significantly more sensitive to neutralization by PGT128 and PGT121 (P=0.03 in both cases), but there were no differences for the other bNAbs. Overall, subtype A variants were significantly more sensitive to NIH45-46 (P=0.04), VRC01 (P=0.002) and PGT145 (P=0.03) compared with the nonsubtype A and less sensitive to PGT121 than subtype Cs (P=0.0001).

CONCLUSION

A combination of bNAbs against distinct epitopes may be needed to provide maximum coverage against viruses in different modes of transmission and diverse subtypes.

摘要

背景

为了预防 HIV 感染,被动转移和/或疫苗诱导的中和抗体(NAb)需要有效地针对全球传播的不同亚型。这些变体是慢性感染期间存在的变体的有限子集,并且具有一些独特的特征。在母婴传播(MTCT)的情况下,传播的变体往往对母体自身 NAb 的中和具有抗性。

方法

为了研究 MTCT 期间传播的变体是否通常对 HIV-1 特异性 NAb 具有抗性,测试了代表主要 HIV-1 亚型的 107 种母体或婴儿变体对六种最近鉴定的 HIV-1 特异性广泛中和单克隆抗体(bNAb),NIH45-46W、VRC01、PGT128、PGT121、PG9 和 PGT145。

结果

婴儿和母体变体在对单个 bNAb 的中和敏感性方面没有差异,也没有来自传播母亲和非传播母亲的病毒之间的差异,尽管来自传播母亲的病毒总体上敏感性较低的趋势。没有单一的 bNAb 能中和所有的病毒,但针对不同表位的 bNAb 组合能覆盖 100%的测试变体。与异性传播变体相比,垂直传播变体对 PGT128 和 PGT121 的中和敏感性显著更高(两种情况下均为 P=0.03),但对其他 bNAb 则没有差异。总体而言,与非亚型 A 相比,亚型 A 变体对 NIH45-46(P=0.04)、VRC01(P=0.002)和 PGT145(P=0.03)的敏感性显著更高,而对 PGT121 的敏感性低于亚型 C(P=0.0001)。

结论

针对不同传播模式和不同亚型的不同表位的 bNAb 组合可能需要提供最大的覆盖范围。

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