Animal models paving the way for clinical trials of attenuated Salmonella enterica serovar Typhi live oral vaccines and live vectors

被引:89
作者
Pasetti, MF [1 ]
Levine, MM [1 ]
Sztein, MB [1 ]
机构
[1] Univ Maryland, Sch Med, Ctr Vaccine Dev, Baltimore, MD 21201 USA
关键词
Salmonella; live vector vaccines; animal models;
D O I
10.1016/S0264-410X(02)00472-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Attenuated Salmonella enterica serovar Typhi (S. Typhi) strains can serve as safe and effective oral vaccines to prevent typhoid fever and as live vectors to deliver foreign antigens to the immune system, either by the bacteria expressing antigens through prokaryotic expression plasmids or by delivering foreign genes carried on eukaryotic expression systems (DNA vaccines). The practical utility of such live vector vaccines relies on achieving a proper balance between minimizing the vaccine's reactogenicity and maximizing its immunogenicity. To advance to clinical trials, vaccine candidates need to be pre-clinically evaluated in relevant animal models that attempt to predict what their safety and immunogenicity profile will be when administered to humans. Since S. Typhi is a human-restricted pathogen, a major obstacle that has impeded the progress of vaccine development has been the shortcomings of the animal models available to assess vaccine candidates. In this review, we summarize the usefulness of animal models in the assessment of the degree of attenuation and immunogenicity of novel attenuated S. Typhi strains as vaccine candidates for the prevention of typhoid fever and as live vectors in humans. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:401 / 418
页数:18
相关论文
共 241 条
[71]   Recombinant attenuated bacteria for the delivery of subunit vaccines [J].
Gentschev, I ;
Dietrich, G ;
Spreng, S ;
Kolb-Mäurer, A ;
Brinkmann, V ;
Grode, L ;
Hess, J ;
Kaufmann, SHE ;
Goebel, W .
VACCINE, 2001, 19 (17-19) :2621-2628
[72]  
Gentschev I, 1997, Behring Inst Mitt, P103
[73]  
GERICHTER C. B., 1960, JOUR HYG, V58, P307
[74]   IMMUNITY IN EXPERIMENTAL SALMONELLOSIS .2. BASIS FOR AVIRULENCE AND PROTECTIVE CAPACITY OF GAL-E MUTANTS OF SALMONELLA-TYPHIMURIUM [J].
GERMANIER, R ;
FURER, E .
INFECTION AND IMMUNITY, 1971, 4 (06) :663-+
[75]  
Gherardi MM, 2000, FEMS IMMUNOL MED MIC, V29, P81
[76]   ANATOMICAL AND IMMUNOLOGICAL RESPONSES OF RABBIT GALLBLADDERS TO BACTERIAL-INFECTIONS [J].
GILMAN, RH ;
YOUNG, C ;
BULGER, R ;
HORNICK, RB ;
GREENBERG, B .
INFECTION AND IMMUNITY, 1982, 36 (01) :407-416
[77]   Expression, extracellular secretion, and immunogenicity of the Plasmodium falciparum sporozoite surface protein 2 in Salmonella vaccine strains [J].
Gómez-Duarte, OG ;
Pasetti, MF ;
Santiago, A ;
Sztein, MB ;
Hoffman, SL ;
Levine, MM .
INFECTION AND IMMUNITY, 2001, 69 (02) :1192-1198
[78]   Protection of mice against gastric colonization by Helicobacter pylori by single oral dose immunization with attenuated Salmonella typhimurium producing urease subunits A and B [J].
Gómez-Duarte, OG ;
Lucas, B ;
Yan, ZX ;
Panthel, K ;
Haas, R ;
Meyer, TF .
VACCINE, 1998, 16 (05) :460-471
[79]   SALMONELLA-TYPHI VACCINE STRAIN CVD-908 EXPRESSING THE CIRCUMSPOROZOITE PROTEIN OF PLASMODIUM-FALCIPARUM - STRAIN CONSTRUCTION AND SAFETY AND IMMUNOGENICITY IN HUMANS [J].
GONZALEZ, C ;
HONE, D ;
NORIEGA, FR ;
TACKET, CO ;
DAVIS, JR ;
LOSONSKY, G ;
NATARO, JP ;
HOFFMAN, S ;
MALIK, A ;
NARDIN, E ;
SZTEIN, MB ;
HEPPNER, DG ;
FOUTS, TR ;
ISIBASI, A ;
LEVINE, MM .
JOURNAL OF INFECTIOUS DISEASES, 1994, 169 (04) :927-931
[80]   Bacteria as gene delivery vectors for mammalian cells - Commentary [J].
Grillot-Courvalin, C ;
Goussard, S ;
Courvalin, P .
CURRENT OPINION IN BIOTECHNOLOGY, 1999, 10 (05) :477-481