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Schistosoma japonicum triose-phosphate isomerase plasmid DNA vaccine protects pigs against challenge infection

Published online by Cambridge University Press:  12 September 2005

Y. ZHU
Affiliation:
Jiangsu Institute of Parasitic Diseases, Wuxi, Jiangsu 214064 P.R. China
J. SI
Affiliation:
Jiangsu Institute of Parasitic Diseases, Wuxi, Jiangsu 214064 P.R. China
D. A. HARN
Affiliation:
Department of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, USA
M. XU
Affiliation:
Jiangsu Institute of Parasitic Diseases, Wuxi, Jiangsu 214064 P.R. China
J. REN
Affiliation:
Jiangsu Institute of Parasitic Diseases, Wuxi, Jiangsu 214064 P.R. China
C. YU
Affiliation:
Jiangsu Institute of Parasitic Diseases, Wuxi, Jiangsu 214064 P.R. China
Y. LIANG
Affiliation:
Jiangsu Institute of Parasitic Diseases, Wuxi, Jiangsu 214064 P.R. China
X. YIN
Affiliation:
Jiangsu Institute of Parasitic Diseases, Wuxi, Jiangsu 214064 P.R. China
W. HE
Affiliation:
Jiangsu Institute of Parasitic Diseases, Wuxi, Jiangsu 214064 P.R. China
G. CAO
Affiliation:
Jiangsu Institute of Parasitic Diseases, Wuxi, Jiangsu 214064 P.R. China

Abstract

The protective efficacy of a Schistosoma japonicum, Chinese strain, triose-phosphate isomerase (TPI) plasmid DNA vaccine was examined in naïve pigs. Pigs were vaccinated with the TPI DNA-plasmid alone, or in conjunction with IL-12 as pcDNA3.1-P35, pcDNA3.1-P40 plasmids via intramuscular injection. Control pigs were immunized with equivalent amounts of pcDNA3.1. Pigs were immunized 3 times at 21-day intervals and challenged 30 days after the final boost. Forty-five days post-challenge, pigs were sacrificed and perfused to compare adult worm burdens, female worm burdens, liver egg burdens and granuloma size. We found that pigs vaccinated with SjCTPI DNA alone had adult worm burdens reduced by 48·3% and that a further decrease in adult worm burdens was not seen in the group vaccinated with SjCTPI DNA in conjunction with IL-12 (46·2% reduction). The SjCTPI DNA vaccines had a more pronounced effect on reducing female worm burdens i.e. 53·6% SjCTPI alone and 59·6% for SjCTPI+IL-12. Vaccination with SjCTPI-DNA reduced liver eggs by 49·4% and this response was significantly enhanced by the addition of IL-12 (65·8% reduction in liver eggs). In addition to the dramatic protective effects seen in vaccinated pigs, we also noted that granuloma size was reduced by 42% in both groups. Thus, vaccination of pigs and other large animals in China with SjCTPI DNA vaccine will likely reduce transmission by reducing adult worm burdens and worm egg output and simultaneously reduce hepatic egg-associated pathology.

Type
Research Article
Copyright
© 2005 Cambridge University Press

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References

REFERENCES

Bergquist, N. R. ( 1995). Controlling schistosomiasis by vaccination: a realistic option? Parasitology Today 11, 191194.Google Scholar
Chitsulo, L., Engels, D., Montressor, A. and Savioli, L. ( 2000). The global status of schistosomiasis and its control. Acta Tropica 77, 4151.CrossRefGoogle Scholar
Department of Diseases Control ( 2001). Minsistry of Health Handbook on Schistosomiasis Control (3rd Edn). Shanghai Science and Technology Press, Shanghai.
Harn, D. A., Gu, W., Oligino, L. D., Mitsuyama, M., Gebremicheal, A. and Richter, D. ( 1992). A protective monoclonal antibody specifically recognizes and alters the catalytic activity of schistosome triose-phosphate isomerase. Journal of Immunology 148, 562567.Google Scholar
Harn, D. A., Mitsuyama, M., Huguenel, E. D., Oligino, L. and David, J. R. ( 1985). Identification by monoclonal antibody of a major (28 kDa) surface membrane antigen of Schistosoma mansoni. Molecular and Biochemical Parasitology 16, 345354.CrossRefGoogle Scholar
Jin, P. ( 1993). Statistical Method for Medicine (1st Edn). Shanghai Medical University Press, Shanghai.
Office of Endemic Diseases Control ( 1998). Ministry of Health, Expert Advisory Committee on Schistosomiasis Ministry of Health, Institute of Parasitic Diseases, Chinese Academy of Preventive Medicine. Epidemic Status of Schistosomiasis in China – A Nation-wide Sampling Survey in 1995. Nanjing University Press, Nanjing.
Robinson, H. L. and Torres, C. T. ( 1997). DNA vaccine. Immunology 9, 271283.Google Scholar
Yoshimoto, T., Kojima, K., Funakoshi, T., Endo, Y., Fujita, T. and Nariuchi, H. ( 1996). Molecular cloning and characterization of murine IL-12 genes. Journal of Immunology 156, 10821088.Google Scholar
Yu, C., Zhu, Y., Yin, X. and Si, J. ( 1997). Gene cloning and sequencing of triose-phosphate isomerase of Schistosoma japonicum Chinese strain (SjCTPI). Chinese Journal of Schistosomiasis Control 9, 321325.Google Scholar
Yu, C., Zhu, Y., Yin, X., Xu, Y., He, W. and Guang, X. ( 1999). The protective effect of recombinant triose phosphate isomerase (rTPI) of Schistosoma japonicum Chinese strain in immunized mice. Chinese Journal of Schistosomiasis Control 11, 267269.Google Scholar
Zhu, Y., Si, J., Harn, D. A., Yu, C., He, W., Hua, W., Yin, X., Liang, Y., Xu, M. and Xu, Y. ( 2002). The protective immunity produced in C57BL/6 mice of DNA vaccine encoding Schistosoma japonicum chinese strain triose-phosphate isomerase. Southeast Asian Journal of Tropical Medicine and Public Health 33, 207213.Google Scholar
Zhu, Y., Si, J., Harn, D. A., Yu, C., Liang, Y., Ren, J., Yin, X. and He, W. ( 2004). The protective immunity of a DNA vaccine encoding Schistosoma japonicum Chinese strain triose-phosphate isomerase in infected BALB/C mice. Southeast Asian Journal of Tropical Medicine and Public Health 35, 518522.Google Scholar