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1型人类免疫缺陷病毒的中和抗体与围产期传播。纽约市围产期HIV传播协作研究组。

Neutralizing antibody and perinatal transmission of human immunodeficiency virus type 1. New York City Perinatal HIV Transmission Collaborative Study Group.

作者信息

Hengel R L, Kennedy M S, Steketee R W, Thea D M, Abrams E J, Lambert G, McDougal J S

机构信息

Department of Medicine, Emory University, Atlanta, Georgia 30303, USA.

出版信息

AIDS Res Hum Retroviruses. 1998 Apr 10;14(6):475-81. doi: 10.1089/aid.1998.14.475.

Abstract

The major immunologic determinants for perinatal transmission of human immunodeficiency virus type 1 (HIV-1) remain largely unknown. The presence of maternal neutralizing antibodies has been proposed as an explanation for why the majority of infants born to untreated HIV-1-infected women do not become infected. Using maternal and infant specimens collected as part of a longitudinal cohort study of perinatal transmission in New York City between 1991 and 1995, we successfully obtained primary viral isolates from 10 of 20 perinatally nontransmitting (NTR) women, 14 of 20 perinatally transmitting (TR) women, and 13 of 13 of their HIV-1-infected infants. Neutralizing antibody titers were then determined using a titer reduction assay. TR and NTR women did not differ in their ability to neutralize autologous virus or laboratory strains LAI and MN. Infant viruses were not less sensitive to neutralization by maternal sera than autologous viruses. Similarly, TR and NTR isolates were neutralized equally well using a reference serum with broad neutralizing ability. Finally, a heteroduplex tracking assay (HTA) was used to analyze the degree of viral homology within 13 TR maternal-infant pairs. In eight pairs, maternal and infant isolates were highly homologous. In five pairs, lesser degrees of homology were observed, consistent with perinatal transmission of a minor species. However, these isolates were no more or less resistant to maternal sera than were homologous isolates. Thus we found no association between the presence of neutralizing antibody in maternal sera as measured by a titer reduction neutralization (inactivation) assay and perinatal transmission of HIV-1.

摘要

人类免疫缺陷病毒1型(HIV-1)围产期传播的主要免疫决定因素在很大程度上仍不清楚。母体中和抗体的存在被认为可以解释为什么大多数未接受治疗的HIV-1感染女性所生的婴儿没有被感染。利用1991年至1995年在纽约市进行的围产期传播纵向队列研究中收集的母体和婴儿标本,我们成功地从20名围产期未传播(NTR)女性中的10名、20名围产期传播(TR)女性中的14名以及她们13名HIV-1感染婴儿中的13名获得了原始病毒分离株。然后使用滴度降低试验测定中和抗体滴度。TR和NTR女性在中和自身病毒或实验室菌株LAI和MN的能力上没有差异。婴儿病毒对母体血清中和的敏感性并不低于自身病毒。同样,使用具有广泛中和能力的参考血清对TR和NTR分离株进行中和的效果相同。最后,使用异源双链追踪分析(HTA)来分析13对TR母婴对中病毒的同源程度。在8对中,母体和婴儿分离株高度同源。在5对中,观察到较低程度的同源性,这与次要毒株的围产期传播一致。然而,这些分离株对母体血清的抗性并不比同源分离株更强或更弱。因此,我们发现通过滴度降低中和(灭活)试验测定的母体血清中中和抗体的存在与HIV-1的围产期传播之间没有关联。

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