围产期艾滋病毒传播的事实和争议。

Immunodeficiency reviews Pub Date : 1992-01-01
J F Delfraissy, S Blanche, C Rouzioux, M J Mayaux
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引用次数: 0

摘要

1992年,儿童感染艾滋病毒主要是由于纵向或围产期传播,即从母亲传染给胎儿和新生儿。这在非洲是一个特别严重的公共卫生问题,在一些郊区,受感染的育龄妇女比例高达20%。在过去几年中,确立了三个要点。(i)在欧洲和北美,围产期传播率在15%至25%之间,在各种前瞻性队列中似乎随着时间的推移保持相对稳定。㈡为确定早期诊断婴儿感染艾滋病毒的最佳方法作出了相当大的努力。目前,通过聚合酶链反应进行病毒培养和HIV DNA基因扩增是最有希望在生命最初6个月内进行早期诊断的方法。(三)最后,受感染婴儿的病程有很好的特点,主要有两种形式————早期和严重疾病或缓慢进行性感染:此外,现在的随访足以证实,在15个月时检测呈阴性的儿童确实未受感染。然而,在一些重要领域缺乏知识。这些因素包括传播的确切时间(在子宫内、分娩期间或产后)、每个时期传播的相对频率、所涉及的机制(特别是胎盘的作用),以及最后,母体、胎儿和病毒因素的影响。必须迅速找到答案,以便开发预防疗法,确定可能有更大传播病毒风险的妇女,开发可靠的产前诊断测试,最后能够更好地向艾滋病毒血清检测呈阳性的妇女通报相关风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Perinatal HIV transmission facts and controversies.

In 1992, HIV infection in children is essentially due to vertical or perinatal transmission, i.e. from the mother to the fetus and neonates. This is a particularly serious public-health problem in Africa where the percentage of infected women of child bearing age is as high as 20% in some suburban areas. During the last few years, three important points have been established. (i) In Europe and North America, the rate of perinatal transmission is between 15 and 25% and appears to have remained relatively stable with time in various prospective cohorts. (ii) Considerable efforts have been directed at defining the optimal methods for early diagnosis of HIV infection in the infants. At present viral cultures and gene amplification of HIV DNA by polymerase chain reaction are the most promising procedures for early diagnosis within the first 6 months of life. (iii) Finally, the course of the disease in the infected infant has been well characterised, it takes two main forms--that of an early and severe disease or that of a slowly progressive infection: In addition, follow-up is now sufficient to confirm that children with negative tests at 15 months are indeed uninfected. However, knowledge is lacking in a number of essential areas. These include the exact timing of transmission (in utero, during delivery or post-partum), the relative frequency of transmission during each period, the mechanism(s) involved (particularly the role of the placenta), and, finally, the influence of maternal, fetal and viral factors. Answers must be found rapidly in order to develop preventive therapy, to identify women who may have an increased risk of transmitting the virus, to develop a reliable antenatal diagnostic test and, finally, to be in a better position to inform HIV-seropositive women of the relative risks.

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