Cestode vaccines: origins, current status and future prospects

被引:86
作者
Lightowlers, M. W. [1 ]
机构
[1] Univ Melbourne, Ctr Vet Clin, Werribee, Vic 3030, Australia
基金
英国惠康基金;
关键词
cysticercosis; hydatidosis; echinococcosis; Taenia; Echinococcus; vaccine; orphan vaccine;
D O I
10.1017/S003118200600179X
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
Recombinant vaccines have been developed which are highly effective in preventing infection with Taenia ovis in sheep, Taenia saginata in cattle, Taenia solium in pigs and Echinococcus granulosus in livestock animals. T. ovis and T. saginata are economically significant parasites and the commercial success or otherwise of vaccines against them will rely on their economic value. E. granulosus and T. solium are zoonotic parasites that cause cystic hydatid disease and neurocysticercosis, respectively, in humans. Vaccines against these parasites have been developed to assist with the control of transmission of the human diseases rather than for prevention of infections in livestock per se. Regions of high prevalence for cystic hydatid disease and neurocysticercosis occur primarily in the developing world. As a consequence, vaccines against them are of little or no commercially interest-they are Orphan Vaccines. Lack of commercial interest in these vaccines has made public sector support for their development necessary well beyond the research phase trough into completion of commercial scale-up and other more commercially-related assessments. Practical use of the vaccines will require commercial-scale production according to international manufacturing standards. Identifying partners and support in this endeavour is now of prime importance in efforts to achieve the potential of these vaccines as new tools for the control of cystic hydatid disease and neurocysticercosis.
引用
收藏
页码:S27 / S42
页数:16
相关论文
共 93 条
[1]  
Batson A, 2002, Dev Biol (Basel), V110, P15
[2]  
BIGGS MW, 1965, CANCER RES, V25, P1888
[3]  
Boa M, 2003, ACTA TROP, V87, P7, DOI [10.1016/S0001-706X(03)00068-8, 10.1016/S0001-706X(03)00117-7]
[4]   STUDIES ON STAGE-SPECIFIC IMMUNITY AGAINST TAENIA-TAENIAEFORMIS METACESTODES IN MICE [J].
BOGH, HO ;
RICKARD, MD ;
LIGHTOWLERS, MW .
PARASITE IMMUNOLOGY, 1988, 10 (03) :255-264
[5]   STAGE-SPECIFIC IMMUNITY TO TAENIA-TAENIAEFORMIS INFECTION IN MICE - A HISTOLOGICAL STUDY OF THE COURSE OF INFECTION IN MICE VACCINATED WITH EITHER ONCOSPHERE OR METACESTODE ANTIGENS [J].
BOGH, HO ;
LIGHTOWLERS, MW ;
SULLIVAN, ND ;
MITCHELL, GF ;
RICKARD, MD .
PARASITE IMMUNOLOGY, 1990, 12 (02) :153-162
[6]   Use of disability adjusted life years in the estimation of the disease burden of echinococcosis for a high endemic region of the Tibetan plateau [J].
Budke, CM ;
Qiu, JM ;
Zinsstag, J ;
Wang, QA ;
Torgerson, PR .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2004, 71 (01) :56-64
[7]   Active immunization of albino rats with protein fractions from Taenia taeniaeformis and its larval form Cysticercus fasciolaris [J].
Campbell, D .
AMERICAN JOURNAL OF HYGIENE, 1936, 23 (01) :104-113
[8]   Methods for assessing the burden of parasitic zoonoses: echinococcosis and cysticercosis [J].
Carabin, H ;
Budke, CM ;
Cowan, LD ;
Willingham, AL ;
Torgerson, PR .
TRENDS IN PARASITOLOGY, 2005, 21 (07) :327-333
[9]   Parasite vaccine development: Large-scale recovery of immunogenic Taenia ovis fusion protein GST-45W(B/X) from Escherichia coli inclusion bodies [J].
Dempster, RP ;
Robinson, CM ;
Harrison, GBL .
PARASITOLOGY RESEARCH, 1996, 82 (04) :291-296
[10]   MATERNAL TRANSFER OF PROTECTION FROM ECHINOCOCCUS-GRANULOSUS INFECTION IN SHEEP [J].
DEMPSTER, RP ;
HARRISON, GBL ;
BERRIDGE, MV .
RESEARCH IN VETERINARY SCIENCE, 1995, 58 (03) :197-202