Building collaborative networks for HIV/AIDS vaccine development: the AVIP experience.

Springer seminars in immunopathology Pub Date : 2006-11-01 Epub Date: 2006-09-16 DOI:10.1007/s00281-006-0026-3
Flavia Ferrantelli, Stefano Buttò, Aurelio Cafaro, Britta Wahren, Barbara Ensoli
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引用次数: 7

Abstract

The need for an effective HIV/AIDS vaccine is imperative to halt a pandemic that involves more than 40 million individuals worldwide as of 2005 and is causing enormous socio-economic losses, especially in developing countries (DC). The overall failure of more than two decades of HIV vaccine research justifies the demands for a concerted effort for the rapid development of new and efficacious vaccines against HIV/AIDS. In this context, building international collaborative networks is a must for speeding up scientific research and optimizing the use of funding in a synergistic fashion, as resources for HIV/AIDS are limited and do not involve most of the biggest Pharmas that are more interested in drug discovery. The AIDS Vaccine Integrated Project (AVIP) consortium is an example of synergistic partnership of international European Union and DC experts with a common research goal. AVIP is a European Commission-funded (FP-6), consortium-based, 5-year program directed to the fast development of new HIV/AIDS vaccine candidates to be tested in phase I clinical trials in Europe for future advancement to phase II/III testing in DC. To ensure their rapid development, AVIP novel combined vaccines include both regulatory and structural HIV antigens, which have already been tested, as single components, in phase I clinical trials. In particular, such combination vaccines may be superior to earlier vaccine candidates, the vast majority of which are based only on either structural or regulatory HIV products. In fact, the generation of immune responses to both types of viral antigens expressed either early (regulatory products) or late (structural products) during the viral life cycle can maximize immune targeting of both primary or chronic viral infection. Further, the rational design of combined vaccines allows exploitation of immunomodulatory functions of HIV regulatory proteins, which can improve immunity against structural vaccine components. The building of the AVIP consortium and its scientific strategy will be reviewed in this paper as an example of the establishment of a consortium regulated by a specific intellectual property agreement.

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建立艾滋病毒/艾滋病疫苗开发的合作网络:AVIP的经验。
必须有一种有效的艾滋病毒/艾滋病疫苗,才能制止这一流行病,截至2005年,全世界有4 000多万人感染这一流行病,并造成巨大的社会经济损失,特别是在发展中国家。20多年来艾滋病毒疫苗研究的全面失败证明,有必要作出协调一致的努力,迅速开发新的有效的艾滋病毒/艾滋病疫苗。在这种情况下,建立国际合作网络是加快科学研究和以协同方式优化资金使用的必要条件,因为用于艾滋病毒/艾滋病的资源是有限的,而且大多数对药物发现更感兴趣的大型制药公司都没有参与。艾滋病疫苗综合项目(avp)联盟是国际欧洲联盟和DC专家为共同研究目标建立协同伙伴关系的一个例子。avp是欧盟委员会资助的(FP-6)、以联盟为基础的5年计划,旨在快速开发新的艾滋病毒/艾滋病候选疫苗,在欧洲进行I期临床试验,以便将来推进到DC的II/III期试验。为了确保它们的快速开发,新型AVIP联合疫苗包括了已经在I期临床试验中作为单一成分进行了测试的调节性和结构性艾滋病毒抗原。特别是,这种联合疫苗可能优于早期的候选疫苗,其中绝大多数仅基于结构性或调节性艾滋病毒产品。事实上,在病毒生命周期中,对两种类型的病毒抗原的早期表达(调节产物)或晚期表达(结构产物)产生免疫应答,可以最大限度地提高对原发性或慢性病毒感染的免疫靶向。此外,合理设计联合疫苗可以利用HIV调节蛋白的免疫调节功能,从而提高对结构性疫苗成分的免疫力。本文将以特定知识产权协议规制下的联盟建立为例,回顾avp联盟的建立及其科学战略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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