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人类免疫缺陷病毒1型母婴传播:与早产或低抗gp120的关联。

Mother-to-infant transmission of human immunodeficiency virus type 1: association with prematurity or low anti-gp120.

作者信息

Goedert J J, Mendez H, Drummond J E, Robert-Guroff M, Minkoff H L, Holman S, Stevens R, Rubinstein A, Blattner W A, Willoughby A

机构信息

Viral Epidemiology Section, National Cancer Institute, Bethesda, Maryland.

出版信息

Lancet. 1989 Dec 9;2(8676):1351-4. doi: 10.1016/s0140-6736(89)91965-x.

DOI:10.1016/s0140-6736(89)91965-x
PMID:2574302
Abstract

In a prospective study of pregnant women infected with human immunodeficiency virus type 1 (HIV-1) in Brooklyn, New York, USA, 16 (29%) of 55 evaluable infants were infected with HIV-1. 9 infants had paediatric acquired immunodeficiency syndrome, 6 had less severe clinical manifestations of HIV-1 infection, and 1 was symptom-free but was seropositive for HIV-1 beyond 15 months of age. The 10 infants born at 37 weeks of gestation or earlier were at higher risk of HIV-1 infection than infants born at 38 weeks of gestation or later (60% vs 22%) but the median age at appearance of disease was approximately 5 months in both groups. The HIV-1 transmission rate was not associated with predelivery levels of maternal T cells, anti-p24, or neutralising antibodies but it was higher, among full-term infants, for those with mothers in the lowest third of the distribution of anti-gp120 levels (53%). On immunoblot, transmitting mothers lacked a gp120 band but not other bands. Protection was not associated with antibody to recombinant peptides from the hypervariable region of the major neutralising gp120 epitope, and the anti-gp120 endpoint dilution titre was similar in transmitting and non-transmitting mothers. Mothers of uninfected full-term infants appear to confer immunological protection against HIV-1 infection of their offspring by way of a high-affinity antibody to a gp120 epitope, whose specificity has importance for vaccine development and possibly perinatal immunotherapy.

摘要

在美国纽约布鲁克林区进行的一项针对感染1型人类免疫缺陷病毒(HIV-1)的孕妇的前瞻性研究中,55名可评估婴儿中有16名(29%)感染了HIV-1。9名婴儿患有儿童获得性免疫缺陷综合征,6名有HIV-1感染的较轻临床表现,1名无症状但在15个月龄后HIV-1血清学呈阳性。孕37周或更早出生的10名婴儿比孕38周或更晚出生的婴儿感染HIV-1的风险更高(60%对22%),但两组出现疾病的中位年龄均约为5个月。HIV-1传播率与产前母体T细胞、抗p24或中和抗体水平无关,但在足月儿中,母亲抗gp120水平处于分布最低三分之一的婴儿传播率更高(53%)。在免疫印迹分析中,传播HIV-1的母亲缺乏gp120条带但其他条带正常。保护作用与针对主要中和gp120表位高变区重组肽的抗体无关,传播和未传播HIV-1的母亲的抗gp120终点稀释滴度相似。未感染足月儿的母亲似乎通过针对gp120表位的高亲和力抗体为其后代提供针对HIV-1感染的免疫保护,该抗体的特异性对疫苗开发以及可能的围产期免疫治疗具有重要意义。

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