DNA-based vaccines protect against zoonotic schistosomiasis in water buffalo

被引:109
作者
Da'Dara, Akram A. [1 ]
Li, Yuesheng S. [2 ,3 ]
Xiong, Tie [2 ]
Zhou, Jie [2 ]
Williams, Gail M. [4 ]
McManus, Donald R. [3 ]
Feng, Zheng [5 ]
Yu, Xin L. [2 ]
Gray, Darren J. [4 ]
Harn, Donald A. [1 ]
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[2] WHO Collaborating Ctr Res & Control Schistosomias, Hunan Inst Parasite Dis, Yueyang 414000, Hunan, Peoples R China
[3] Queensland Inst Med Res, Div Infect Dis & Immunol, Mol Parasitol Lab, Brisbane, Qld 4029, Australia
[4] Univ Queensland, Sch Populat Hlth, Herston, Qld 4006, Australia
[5] Chinese Ctr Control & Prevent, Natl Inst Parasit Dis, Shanghai 200025, Peoples R China
基金
英国惠康基金;
关键词
Schistosoma japonicum; DNA vaccine; water buffaloes; SjCTPI-Hsp70; SjC23-Hsp70; IL-12;
D O I
10.1016/j.vaccine.2008.04.080
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Schistosomiasis japonica is an endemic, zoonotic disease of major public health importance in China where water buffaloes account for approximately 75% of disease transmission. Interventions that reduce schistosome infection in water buffaloes will enhance their health simultaneously reducing disease transmission to humans. While chemotherapy has proved successful, it requires continued time consuming and expensive mass treatments. A more sustainable option would be development of vaccines that reduce transmission of S. japonicum from bovines to replace bovine chemotherapy. We performed two randomized double blind trials in water buffaloes to determine if DNA vaccines encoding triose-phosphate isomerase (SjCTPI), or the tetraspanin 23 kDa integral membrane protein (SjC23), alone or fused to bovine heat shock protein 70 (Hsp70) could induce a level of immunity conducive to long-term sustainable control. Groups of water buffaloes (15/group) received three intramuscular injections, 4 weeks apart. Booster immunizations were co-administered with a plasmid DNA encoding IL-12. Four weeks after the last injection, water buffaloes were challenged with 1000 cercariae, and vaccine efficacy analyzed 8 weeks later. Water buffaloes vaccinated with SjCTPI-Hsp70 or SjCTPI plasmids had worm burdens reduced by 51.2% and 41.5%, respectively. Importantly, fecal miracidial hatching was reduced by 52.1% and 33.2% respectively compared to control vaccinated water buffaloes. Vaccination with SjC23-Hsp70 and SjC23 plasmids reduced worm burdens by 50.9% and 45.5%, respectively, and fecal miracidial hatching by 52.0% and 47.4%. A mathematical model of schistosome transmission predicts that schistosome vaccines capable of reducing water buffaloes' fecal egg output by 45%, alone or in conjunction with praziquantel treatment, will lead to a significant reduction in transmission of schistosomiasis. Both DNA vaccines tested here exceed this hypothetical level. Indeed, mathematical modeling of SjCTPI-Hsp70 and SjC23-Hsp70 alone and in conjunction with human chemotherapy showed a significant reduction in transmission almost to the point of elimination. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3617 / 3625
页数:9
相关论文
共 63 条
[1]   HSP70 stimulates cytokine production through a CD14-dependant pathway, demonstrating its dual role as a chaperone and cytokine [J].
Asea, A ;
Kraeft, SK ;
Kurt-Jones, EA ;
Stevenson, MA ;
Chen, LB ;
Finberg, RW ;
Koo, GC ;
Calderwood, SK .
NATURE MEDICINE, 2000, 6 (04) :435-442
[2]   ANTIBODY-RESPONSE OF SCHISTOSOMA-MANSONI-INFECTED HUMAN-SUBJECTS TO THE RECOMBINANT P-28-GLUTATHIONE-S-TRANSFERASE AND TO SYNTHETIC PEPTIDES [J].
AURIAULT, C ;
GRASMASSE, H ;
PIERCE, RJ ;
BUTTERWORTH, AE ;
WOLOWCZUK, I ;
CAPRON, M ;
OUMA, JH ;
BALLOUL, JM ;
KHALIFE, J ;
NEYRINCK, JL ;
TARTAR, A ;
KOECH, D ;
CAPRON, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (09) :1918-1924
[3]   CD91 is a common receptor for heat shock proteins gp96, hsp90, hsp70, and calreticulin [J].
Basu, S ;
Binder, RJ ;
Ramalingam, T ;
Srivastava, PK .
IMMUNITY, 2001, 14 (03) :303-313
[4]   Vaccine-linked chemotherapy: can schistosomiasis control benefit from an integrated approach? [J].
Bergquist, NR ;
Leonardo, LR ;
Mitchell, GF .
TRENDS IN PARASITOLOGY, 2005, 21 (03) :112-117
[5]   CD91: a receptor for heat shock protein gp96 [J].
Binder, RJ ;
Han, DK ;
Srivastava, PK .
NATURE IMMUNOLOGY, 2000, 1 (02) :151-155
[6]   Adjuvanticity of α2-macroglobulin, an independent ligand for the heat shock protein receptor CD91 [J].
Binder, RJ ;
Karimeddini, D ;
Srivastava, PK .
JOURNAL OF IMMUNOLOGY, 2001, 166 (08) :4968-4972
[7]  
Chen XY, 2005, B WORLD HEALTH ORGAN, V83, P43
[8]   Schistosomiasis [J].
Chitsulo, L ;
Loverde, R ;
Engels, D ;
Barakat, R ;
Colley, D ;
Cioli, D ;
Engels, D ;
Feldmeier, H ;
Loverde, P ;
Olds, GR ;
Ourna, J ;
Rabello, A ;
Savioli, L ;
Traore, M ;
Vennerwald, B .
NATURE REVIEWS MICROBIOLOGY, 2004, 2 (01) :12-13
[9]   A DNA-prime/protein-boost vaccination regimen enhances Th2 immune responses but not protection following Schistosoma mansoni infection [J].
DA'Dara, AA ;
Skelly, PJ ;
Walker, CM ;
Harn, DA .
PARASITE IMMUNOLOGY, 2003, 25 (8-9) :429-437
[10]   Comparative efficacy of the Schistosoma mansoni nucleic acid vaccine, Sm23, following microseeding or gene gun delivery [J].
Da'dara, AA ;
Skelly, PJ ;
Fatakdawala, M ;
Visovatti, S ;
Eriksson, E ;
Harn, DA .
PARASITE IMMUNOLOGY, 2002, 24 (04) :179-187