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Opisthorchis viverrini: Partial success in adoptively transferring immunity with spleen cells and serum in the hamster

Published online by Cambridge University Press:  05 June 2009

D. J. Flavell
Affiliation:
Division of Nuclear Medicine, Faculty of Medicine, Siriraj Hospital, Bangkok, Thailand
K. Pattanapanyasat
Affiliation:
Division of Nuclear Medicine, Faculty of Medicine, Siriraj Hospital, Bangkok, Thailand
Sopsamornu U. Flavell
Affiliation:
Department of Clinical Microbiology, Faculty of Medical Technology, Siriraj Hospital, Bangkok, Thailand

Abstract

Three groups of golden Syrian hamsters received intraperitoneally either, (1) 1 × 107 spleen cells, (2) 0.5 ml. serum or, (3) 1 × 107 spleen cells plus 0.5 ml. serum, from donors infected 6 weeks previously with 25 Opisthorchis viverrini metacercariae, one day before and at the same time as challenge with 25 metacercariae. Three groups of control animals received the same quantities of spleen cells, serum or an admixture of both from normal non-infected donors in the same manner followed by challenge with 25 metacercariae.

Animals were killed six weeks after challenge, livers and extrahepatic biliary systems carefully removed, and liver worm burdens estimated. Additionally, parasitic egg counts were performed on pooled faeces samples collected one hour prior to death.

Animals receiving spleen cells, serum, or an admixture of both, from normal non-infected donors had mean worm burdens of 11.44, 12.00 and 12.66, respectively. Animals receiving spleen cells, serum, or both, from infected donors had mean worm burdens of 9.88, 7.77 and 12.00, respectively. There were no significant differences in mean worm burdens between control and experimental groups. However, a substanial reduction in parasitic faecal egg counts and subsequently mean egg production per worm was observed in all 3 groups of animals receiving spleen cells, serum, or both, from infected donors when compared to their respective control group.

These findings are discussed in relation to adoptive transfer studies performed with other helminths and their possible relevance to naturally acquired immunity is commented on.

Type
Research Papers
Copyright
Copyright © Cambridge University Press 1980

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References

REFERENCES

Armour, J. and Dargie, J. D., (1974) Immunity to Fasciola hepatica in the rat. Sucessful transfer of immunity by lymphoid cells and serum. Experimental Parasitology, 35, 381388.CrossRefGoogle Scholar
Bhamarapravati, N., Thammavit, W. and Vajrasthira, S. (1978) Liver changes in hamsters infected with a liver fluke of man, Opisthorchis viverrini. American Journal of Tropical Medicine and Hygiene, 27, 787794.CrossRefGoogle ScholarPubMed
Butterworth, A. E., Remold, H. G. and Houbin, V. (1977) Antibody-dependent eosinophil-mediated damage to 51 CR/-labelled schistosomula of Schstosoma mansoni. Mediation by IgG and inhibition by antigen-antibody complexes. Journal of Immunology, 118, 22302236.CrossRefGoogle Scholar
Eriksen, L. and Flagstad, T. (1974) Fasciola hepatica: Influence of extra-hepatic adult fluke on infections and immunity in rats. Experimental Parasitology, 35, 411417.CrossRefGoogle Scholar
Evans, H., Bourgeois, C. H., Comer, D. H. and Keschamras, N. (1971) Biliary tract changes in opisthorchiasis. American Journal of Tropical Medicine and Hygiene, 20, 667671.CrossRefGoogle ScholarPubMed
Flavell, D. J., Goepel, J., Potter, C. W. and Carr, I. (1978) Cellular immunity to encephalitogenic factor as measured by macrophage migration inhibition during tumour induction and growth. British Journal of Cancer, 38, 818826.CrossRefGoogle Scholar
Flavell, D. J., Pattanapanyasat, K., Lucas, S. B. and Vongsangnak, V. (1980). Opisthorchis viverrini: Liver changes in golden hamsters maintained on high and low protein diets. Acta Tropica, (in press).Google Scholar
Gibson, J. B. and Sun, T. (1971) Clonorchiasis. In Pathology of Protozoal and Helminthic Diseases with Clinical Correlation. pp 546565 (Marcial-Rojas, P. A. ed). Williams and Wilkins: Baltimore.Google Scholar
Goose, J. and McGregor, M. (1973) Naturally acquired immunity to Fasciola hepatica in the rat. British Veterinary Journal, 129, xlix–lii.CrossRefGoogle ScholarPubMed
Harinasuta, C. and Vajrasthira, S. (1960) Opisthorchiasis in Thailand. Annals of Tropical Medicine and Parasitology, 54, 100105.CrossRefGoogle ScholarPubMed
Hou, P. C. (1955) The Pathology of Clonorchis sinensis infestation of the liver. Journal of Pathology and Bacteriology, 70, 5364.Google ScholarPubMed
Hou, P. C. (1956) The relationship between primary carcinoma of the liver and infestation with Clonorchis sinensis. Journal of Pathology and Bacteriology, 72, 239246.Google ScholarPubMed
Keller, R. and Kiest, R. (1972) Protective immunity to Nippostrongylus brasiliensis in the rat. Central role of the lymphocyte in worm expulsion. Immunology, 22, 767773.Google ScholarPubMed
Koompirochana, C., Sonakul, D., Chinda, K. and Stitnimankarn, T. (1978) Opisthorchiasis: A clinical pathologic study of 154 autopsy cases. South-East Asian Journal of Tropical Medicine and Public Health, 9, 6064.Google Scholar
Nelson, G. S., Teesdale, C. and Highton, R. B. (1962) In CIBA Foundation Symposium on Bilharziasis. pp. 127149. (Wostenholme, G. E. W. and O'Connor, M. eds). Churchill: London.CrossRefGoogle Scholar
Pelley, R. P. and Hillyer, G. V. (1978) Demonstration of a common antigen between Schistosoma mansoni and Fasciola hepatica. American Journal of Tropical Medicine and Hygiene., 27, 11921194.CrossRefGoogle ScholarPubMed
Purtilo, D. T. (1976) Clonorchiasis and hepatic neoplasms. Tropical and Geographical Medicine, 28, 2127.Google ScholarPubMed
Sher, A., McIntyre, S. and Lichtenberg, F. (1977) Schistosoma mansoni: Kinetics and class specificity of hypergammaglobulinaemia induced during murine infection. Experimental Parasitology, 41, 415422.CrossRefGoogle ScholarPubMed
Sonakul, D., Koompirochana, C., Chinda, K. and Stitnimankarn, T. (1978) Hepatic carcinoma with opisthorchiasis. South-East Asian Journal of Tropical Medicine and Public Health, 9, 215219.Google ScholarPubMed
Soulsby, E. J. L. (1965) Textbook of Veterinary Clinical Parasitology. Blackwell Scientific Publications: Oxford.Google Scholar
Sun, T. (1969a) The in vitro action of antisera on the adults of Clonorchis sinensis. Transactions of the Royal Society of Tropical Medicine and Hygiene, 63, 582590.CrossRefGoogle ScholarPubMed
Sun, T. (1969b) The non-antigenicity of the intact ova of Clonorchis sinensis. Journal of Medical Microbiology, 2, 582590.CrossRefGoogle ScholarPubMed
Sun, T., Chou, S. T. and Gibson, J. B. (1968) Route of entry of Clonorchis sinensis to the mamalian liver. Experimental parasitology, 22, 346351.CrossRefGoogle Scholar
Sun, T. and Gibson, J. B. (1969a) Metabolic products of adult Clonorchis sinensis: Their composition and antigenic potential. Journal of Helminthology, 43, 395402.CrossRefGoogle ScholarPubMed
Sun, T. and Gibson, J. B. (1969b) The sites of antigen formation in different developmental stages of Clonorchis sinensis. Japanese Journal of Medical Science and Biology, 22, 263271.CrossRefGoogle ScholarPubMed
Webbe, G., James, C., Nelson, G. S., Ismail, M. and Shaw, J. R. (1979) Cross resistance between Schistosoma haematobium and S. mansoni in the baboon. Transactions of the Royal Society of Tropical Medicine and Hygiene, 73, 4254.CrossRefGoogle ScholarPubMed
Wykoff, D. E., Harinasuta, C., Juttijadata, P. and Winn, M. M. (1965) Opisthorchis viverrini in Thailand—The life cycle and comparison with O. felineus. Journal of Parasitology, 51, 207214.CrossRefGoogle ScholarPubMed