Progress in the development of Fasciola hepatica vaccine using recombinant fatty acid binding protein with the adjuvant adaptation system ADAD

被引:36
作者
Lopez-Aban, J.
Casanueva, P.
Nogal, J.
Arias, M.
Morrondo, P.
Diez-Banos, P.
Hillyer, G. V.
Martinez-Fernandez, A. R.
Muro, A.
机构
[1] Univ Salamanca, Fac Farm, Parasitol Lab, E-37007 Salamanca, Spain
[2] Univ Complutense Madrid, Fac Farm, Parasitol Lab, E-28040 Madrid, Spain
[3] Univ Santiago de Compostela, Dept Anim Pathol, Fac Vet, Lugo 27002, Spain
[4] Univ Puerto Rico, Sch Med, Dept Pathol & Lab Med, San Juan, PR 00936 USA
关键词
Fasciola hepatica; FABP; immunomodulator; vaccine; Polypodium leucotomos;
D O I
10.1016/j.vetpar.2006.12.017
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
Fatty acid binding proteins (FABP) have been designed as a potential vaccine against fasciolosis. In this work, the immunoprophylaxis of the recombinant Fh15 FABP from E hepatica (Fh15) in adjuvant/immunomodulator ADAD system was evaluated using mice and sheep challenged with E hepatica. The ADAD system combines the Fh15 antigen with an immunomodulator (hydroalcoholic extract of Polypodium leucotomos; PAL) and/or an adjuvant (saponins of Quillaja saponaria; Qs) in a water/oil emulsion (30/70) with a non-mineral oil (Montanide). All the infected control mice died by 41-48 days postinfection. The mice vaccinated with ADAD only with PAL + Fh15 present a survival rate of 40-50% and those vaccinated with ADAD containing PAL + Qs + Fh15 had a survival rate of 50-62.5%. IgG1 antibodies were lower in surviving mice in comparison with non-surviving mice. The sheep vaccinated with ADAD PAL + Qs + Fh15 showed lower fluke recovery (43%), less hepatic lesions and higher post-infection daily weight gain than F hepatica infected control animals. Thus, the ADAD system using recombinant fatty acid binding proteins from F hepatica could be a good option to develop vaccines against E hepatica. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:287 / 296
页数:10
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