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活病毒和细菌载体在疫苗中的潜在应用。世界卫生组织会议,日内瓦,1989年6月19日至22日。

Potential use of live viral and bacterial vectors for vaccines. WHO meeting, Geneva, 19-22 June, 1989.

出版信息

Vaccine. 1990 Oct;8(5):425-37. doi: 10.1016/0264-410x(90)90241-d.

Abstract

The use of vaccinia virus vector for the delivery of antigens was first described by Moss and Paoletti and their colleagues in 1982. Such vaccines could be of particular value in developing countries because they would be cheap, stable, easy to administer and provide long-lasting immunity. WHO recognized the potential value of such a delivery system by convening two meetings, one at the National Institutes of Health, USA in November 1984 and the second at WHO headquarters, Geneva, Switzerland in September 1985, to discuss the possibility of using such products, particularly with regard to their safety. Since that time, other vehicles which could be useful for the delivery of antigens have been described. These include Escherichia coli, Salmonella typhimurium, BCG, all other poxviruses, adenovirus, herpesvirus and poliovirus. At its meeting in July 1988, the Scientific Advisory Group of Experts of the Programme for Vaccine Development (SAGE) concluded that it was appropriate to discuss the general topic of live vectors and proceeded to arrange a meeting to discuss the present position and to prepare a report on the following key issues: requirements for safety and efficacy; immunological factors which may influence efficacy; medical constraints on use. The present report results from a meeting held in Geneva from 19 to 22 June 1989.

摘要

痘苗病毒载体用于递送抗原最早是由莫斯和保莱蒂及其同事在1982年描述的。这类疫苗在发展中国家可能具有特殊价值,因为它们价格低廉、稳定性好、易于接种且能提供持久免疫力。世界卫生组织认识到这种递送系统的潜在价值,为此召开了两次会议,一次于1984年11月在美国国立卫生研究院召开,另一次于1985年9月在瑞士日内瓦的世界卫生组织总部召开,以讨论使用这类产品的可能性,特别是其安全性。自那时以来,已描述了其他可用于递送抗原的载体。这些包括大肠杆菌、鼠伤寒沙门氏菌、卡介苗、所有其他痘病毒、腺病毒、疱疹病毒和脊髓灰质炎病毒。疫苗开发计划科学咨询专家组(SAGE)在其1988年7月的会议上得出结论,讨论活载体这一总体议题是合适的,并着手安排一次会议来讨论当前状况,并就以下关键问题编写一份报告:安全性和有效性要求;可能影响有效性的免疫学因素;使用方面的医学限制。本报告源自1989年6月19日至22日在日内瓦举行的一次会议。

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