Experimental vaccines against measles in a world of changing epidemiology

被引:25
作者
Pütz, MM
Bouche, FB
de Swart, RL
Muller, CP
机构
[1] Lab Natl Sante, Dept Immunol, L-1950 Luxembourg, Luxembourg
[2] Univ Tubingen, Fak Chem & Pharm, D-72076 Tubingen, Germany
[3] Erasmus MC, Inst Virol, NL-3000 DR Rotterdam, Netherlands
[4] Univ Tubingen, Fak Med, D-72076 Tubingen, Germany
关键词
live attenuated vaccine; measles virus; recombinant protein; synthetic peptide; bacterial vector; viral vector; epidemiology;
D O I
10.1016/S0020-7519(03)00062-6
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
Vaccination with the current live attenuated measles vaccine is one of the most successful and cost-effective medical interventions. However, as a result of persisting maternal antibodies and immaturity of the infant immune system, this vaccine is poorly immunogenic in children <9 months old. Immunity against the live vaccine is less robust than natural immunity and protection less durable. There may also be some concern about (vaccine) virus spread during the final stage of an eventual measles eradication program. Opinions may differ with respect to the potential threat that some of these concerns may be to the World Health Organisation goal of measles elimination, but there is a consensus that the development of new measles vaccines cannot wait. Candidate vaccines are based on vital or bacterial vectors expressing recombinant viral proteins, naked DNA, immune stimulating complexes or synthetic peptides mimicking neutralising epitopes. While some of these candidate vaccines have proven their efficacy in monkey studies, aerosol formulated live attenuated measles vaccine are evaluated in clinical trials. (C) 2003 Australian Society for Parasitology Inc. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:525 / 545
页数:21
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