Pathways and strategies for developing a malaria blood-stage vaccine

被引:127
作者
Good, MF [1 ]
Kaslow, DC
Miller, LH
机构
[1] Queensland Inst Med Res, Cooperat Res Ctr Vaccine Technol, Brisbane, Qld 4029, Australia
[2] NIAID, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
关键词
immune mechanisms; MSP-1; pathogenesis;
D O I
10.1146/annurev.immunol.16.1.57
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In the past 10 years, our knowledge of the malaria parasite has increased enormously: identification and analysis of parasite antigens, demonstration of protection of monkeys and mice following immunization with these antigens, and better understanding of the mechanisms of immunity to malaria and the pathogenesis of disease in malaria. Powerful new adjuvants have been developed, some of which-it is hoped-will be suitable for human use. Recently, a successful human trial of a vaccine aimed at sporozoites (the stage inoculated by mosquitoes) was completed. However, it is the red blood cell stage of the parasite that causes disease, and it is against this stage-in which the parasite grows at an exponential rate-that it has proven very difficult to induce a protective immune response by vaccination. This review focuses on recent exciting developments toward a blood-stage vaccine. We analyze the major obstacles to vaccine development and outline a strategy involving public-and industry-funded research that should result in development of a vaccine.
引用
收藏
页码:57 / 87
页数:31
相关论文
共 95 条
[31]   COMPLEMENT-FIXING IGG1 CONSTITUTES A NEW SUBCLASS OF MOUSE IGG [J].
EY, PL ;
PROWSE, SJ ;
JENKIN, CR .
NATURE, 1979, 281 (5731) :492-493
[32]   Plasmodium falciparum-specific T cell clones from non-exposed and exposed donors are highly diverse in TCR beta chain V segment usage [J].
Fell, AH ;
Silins, SL ;
Baumgarth, N ;
Good, MF .
INTERNATIONAL IMMUNOLOGY, 1996, 8 (12) :1877-1887
[33]  
FRANKE ED, 1997, UNPUB SUBDOMINANT CD
[34]   PLASMODIUM-YOELII - ANTIBODY AND THE MAINTENANCE OF IMMUNITY IN BALB-C MICE [J].
FREEMAN, RR ;
PARISH, CR .
EXPERIMENTAL PARASITOLOGY, 1981, 52 (01) :18-24
[35]  
GOOD M F, 1990, Peptide Research, V3, P110
[36]   IMMUNOLOGICAL RESPONSES FROM NON-EXPOSED DONORS TO MALARIA ANTIGENS - IMPLICATIONS FOR IMMUNITY AND PATHOLOGY [J].
GOOD, MF .
IMMUNOLOGY LETTERS, 1994, 41 (2-3) :123-125
[37]   THE T-CELL RESPONSE TO THE MALARIA CIRCUMSPOROZOITE PROTEIN - AN IMMUNOLOGICAL APPROACH TO VACCINE DEVELOPMENT [J].
GOOD, MF ;
BERZOFSKY, JA ;
MILLER, LH .
ANNUAL REVIEW OF IMMUNOLOGY, 1988, 6 :663-688
[38]   IMMUNITY TO PLASMODIUM-CHABAUDI-ADAMI IN THE B-CELL-DEFICIENT MOUSE [J].
GRUN, JL ;
WEIDANZ, WP .
NATURE, 1981, 290 (5802) :143-145
[39]   SAFETY AND IMMUNOGENICITY IN MAN OF A SYNTHETIC PEPTIDE MALARIA VACCINE AGAINST PLASMODIUM-FALCIPARUM SPOROZOITES [J].
HERRINGTON, DA ;
CLYDE, DF ;
LOSONSKY, G ;
CORTESIA, M ;
MURPHY, JR ;
DAVIS, J ;
BAQAR, S ;
FELIX, AM ;
HEIMER, EP ;
GILLESSEN, D ;
NARDIN, E ;
NUSSENZWEIG, RS ;
NUSSENZWEIG, V ;
HOLLINGDALE, MR ;
LEVINE, MM .
NATURE, 1987, 328 (6127) :257-259
[40]   MOLECULAR ANALYSIS OF THE ASSOCIATION OF HLA-B53 AND RESISTANCE TO SEVERE MALARIA [J].
HILL, AVS ;
ELVIN, J ;
WILLIS, AC ;
AIDOO, M ;
ALLSOPP, CEM ;
GOTCH, FM ;
GAO, XM ;
TAKIGUCHI, M ;
GREENWOOD, BM ;
TOWNSEND, ARM ;
MCMICHAEL, AJ ;
WHITTLE, HC .
NATURE, 1992, 360 (6403) :434-439