The human immunodeficiency virus preventive vaccine research at the French National Agency for acquired immunodeficiency syndrome research

被引:4
|
作者
Fischer, E [1 ]
Rieux, W [1 ]
Guillet, JG [1 ]
Kazatchkine, M [1 ]
机构
[1] Agence Natl Rech SIDA, F-75013 Paris, France
来源
MEMORIAS DO INSTITUTO OSWALDO CRUZ | 2005年 / 100卷 / 01期
关键词
human immunodeficiency virus; vaccine trials; lipopeptides; network;
D O I
10.1590/S0074-02762005000100015
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
The human immunodeficiency virus/acquired immunodeficiency syndrome (HIV/AIDS) epidemic is of unprecedented gravity and is spreading rapidly, notably in the most disadvantaged regions of the world. The search for a preventive vaccine is thus an absolute priority. For over 10 years the French National Agency for AIDS research (ANRS) has been committed to an original program combining basic science and clinical research. The HIV preventive vaccine research program run by the ANRS covers upstream research for the definition of immunogens, animal models, and clinical research to evaluate candidate vaccines. Most researchers in 2004 believe that it should be possible to obtain partial vaccine protection through the induction of a strong and multiepitopic cellular response. Since 1992, the ANRS has set up 15 phases I and II clinical trials in order to evaluate the safety and the capacity of the candidate vaccines for inducing cellular immune responses. The tested candidate vaccines were increasingly complex recombinant canarypox viruses (Alvac) containing sequences coding for certain viral proteins, utilized alone or combined with other immunogens (whole or truncated envelope proteins). ANRS has also been developing an original strategy based on the utilization of lipopeptides. These comprise synthetic fragments of viral proteins associated with lipids that facilitate the induction of a cellular immune response. These approaches promptly allowed the assessment of a prime-boost strategy combining a viral vector and lipopeptides.
引用
收藏
页码:79 / 84
页数:6
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