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孕妇针对gp120 V3环肽的抗体与围产期HIV-1传播之间缺乏相关性。纽约市围产期HIV传播协作研究。

Lack of correlation between maternal antibodies to V3 loop peptides of gp120 and perinatal HIV-1 transmission. The NYC Perinatal HIV Transmission Collaborative Study.

作者信息

Parekh B S, Shaffer N, Pau C P, Abrams E, Thomas P, Pollack H, Bamji M, Kaul A, Schochetman G, Rogers M

机构信息

Division of HIV/AIDS, Centers for Disease Control, Atlanta, Georgia 30333.

出版信息

AIDS. 1991 Oct;5(10):1179-84. doi: 10.1097/00002030-199110000-00004.

Abstract

Recent reports have suggested that maternal antibodies to specific epitopes of the variable region 3 (V3 loop) of gp120 of HIV-1 might protect against perinatal transmission. In an attempt to confirm these findings, sera from 34 HIV-1-seropositive mothers, representing 13 episodes of mother-to-infant transmission and 23 episodes of non-transmission (two mothers had two pregnancies each during the study period), were tested for the presence of antibodies to various regions of the gp120 V3 loop. Synthetic peptides were generated from HIV-1MN. Of the four peptides tested by enzyme-linked immunosorbent assay (ELISA), only antibody to the C53 peptide (Env310-322, principal neutralizing determinant) was present in maternal sera. Antibody to the C53 sequence was present in 11 specimens from transmitting mothers and 21 from non-transmitting mothers (84.6 and 91.3%, respectively, P = 0.6). No reactivity was detected against the C51, C57, or C58 peptide sequences, located on the sides of the V3 loop. In an antigen-limited ELISA, only two specimens from transmitting mothers and two specimens from non-transmitting mothers had detectable 'high-affinity' antibodies to C53 at low antigen concentrations (15.4 and 8.7%, respectively; P = 0.6). Our results do not support previous reports that epitope-specific antibodies to the V3 loop peptides protect against perinatal transmission. Further research is required to determine whether any specific maternal humoral response might influence HIV-1 perinatal transmission.

摘要

最近的报告表明,针对人类免疫缺陷病毒1型(HIV-1)gp120可变区3(V3环)特定表位的母体抗体可能预防围产期传播。为了证实这些发现,对34名HIV-1血清阳性母亲的血清进行了检测,这些母亲代表了13例母婴传播和23例非传播情况(两名母亲在研究期间各有两次怀孕),以检测针对gp120 V3环各个区域的抗体。合成肽由HIV-1MN产生。通过酶联免疫吸附测定(ELISA)检测的四种肽中,母体血清中仅存在针对C53肽(Env310-322,主要中和决定簇)的抗体。来自传播母亲的11份标本和来自非传播母亲的21份标本中存在针对C53序列的抗体(分别为84.6%和91.3%,P = 0.6)。未检测到针对位于V3环两侧的C51、C57或C58肽序列的反应性。在抗原有限的ELISA中,仅来自传播母亲的两份标本和来自非传播母亲的两份标本在低抗原浓度下具有可检测到的针对C53的“高亲和力”抗体(分别为15.4%和8.7%;P = 0.6)。我们的结果不支持先前的报告,即针对V3环肽的表位特异性抗体可预防围产期传播。需要进一步研究以确定任何特定的母体体液反应是否可能影响HIV-1围产期传播。

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