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发展中国家的人类免疫缺陷病毒疫苗研发:疗效试验可行吗?

Human immunodeficiency virus vaccine development in developing countries: are efficacy trials feasible?

作者信息

Excler J L, Beyrer C

机构信息

U.S. Military HIV Research Program, HIV Vaccine Development Program, Rockville, Maryland 20850, USA.

出版信息

J Hum Virol. 2000 Jul-Aug;3(4):193-214.

Abstract

The implementation of human immunodeficiency virus (HIV) vaccine efficacy trials in developing countries represents an unprecedented series of challenges for the medical and scientific communities, health authorities, policy makers, and the populations of diverse countries. Such trials require great attention, dedication, and information at the earliest possible time from many groups in these communities, as well as the clear and full collaboration of all the national and international institutions and agencies involved. This article discusses suggestions and makes recommendations regarding multiple hurdles to trial implementation, including access to appropriate populations, incidence and natural history of HRV type 1 (HIV-1) infection, definition of efficacy endpoints, and logistical, ethical, regulatory, political, and media issues. The conduct of phase I and II trials in developing countries will be a critical step for appropriate vaccine selection and in helping to identify the country- and community-specific issues and the needs for further implementation. Some countries have already established their own national HIV vaccine development plans. Additional operational and action plans with special emphasis on efficacy trial implementation would be strongly recommended after country-specific preparedness workshops and constitution of national or regional task forces.

摘要

在发展中国家开展人类免疫缺陷病毒(HIV)疫苗效力试验,对医学界、科学界、卫生当局、政策制定者以及不同国家的民众而言,是一系列前所未有的挑战。此类试验需要这些群体中的许多团体尽早给予高度关注、全身心投入并提供信息,同时需要所有相关的国家和国际机构及部门进行明确且充分的协作。本文讨论了有关试验实施的多重障碍的建议并提出了相关建议,包括接触合适的人群、1型人免疫缺陷病毒(HIV-1)感染的发病率和自然史、效力终点的定义以及后勤、伦理、监管、政治和媒体问题。在发展中国家开展I期和II期试验,对于选择合适的疫苗以及帮助确定特定国家和社区的问题及进一步实施的需求而言,将是关键的一步。一些国家已经制定了自己的国家HIV疫苗研发计划。在举办针对特定国家的筹备研讨会并组建国家或区域特别工作组之后,强烈建议制定特别强调效力试验实施的额外运营和行动计划。

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