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Effects of adoptive transfer of immune spleen cells on worm growth and microfilaraemia in Brugia pahangi infection in Mongolian gerbils

Published online by Cambridge University Press:  05 June 2009

A.I. Khan
Affiliation:
Department of Parasitology, Miyazaki Medical College, Kiyotake, Miyazaki 889-16, Japan
Y. Horii
Affiliation:
Department of Veterinary Internal Medicine, Faculty of Agriculture, Miyazaki University, Gakuen-Kibanadai, Miyazaki 889-21, Japan
N. Ishikawa
Affiliation:
Department of Parasitology, Miyazaki Medical College, Kiyotake, Miyazaki 889-16, Japan

Abstract

Protective immunity against Brugia pahangi was examined after adoptive transfer of immune spleen cells. Spleen cells obtained from gerbils at 8 weeks post-infection (p.i.) with 100 infective larvae (L3) of B. pahangi were transferred into naive recipients, and then 24 h later, they were infected with 100 L3 of B. pahangi. The recipients given normal spleen cells and infected by the same manner served as controls. Microfilarial counts in the circulation were monitored at designated times after infection and worm burden and the size of individual female worm were determined at 16 weeks p.i. to evaluate the effects of adoptive immunization. In addition, eosinophil responses and serum antibody titres were examined during the course of infection. In the control group, microfilariae first appeared in circulation at 9 weeks p.i. and continuously increased in number throughout the course examined. In contrast, microfilaraemia was almost completely suppressed in the group given immune spleen cells. Although worm burden was comparable between the two groups, the average size of female adult worms recovered from the adoptively immunized group was significantlysmaller than that from the control group. Eosinophil response was hastened and enhanced by adoptive transfer of immune spleen cells in the early stage of infection. Parasite- specific antibody response was also hastened by adoptive immunization. These results suggest that immune spleen cells could confer protective immunity mainly directed against adult B. pahangi.

Type
Research Papers
Copyright
Copyright © Cambridge University Press 1995

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References

Ash, L.R. & Riley, J.M. (1970a) Development of Brugia pahangi in the jird, Meriones unguiculatus, with notes on infections in other rodents. Journal of Parasitology 56, 962968.CrossRefGoogle ScholarPubMed
Ash, L.R. & Riley, J.M. (1970b) Development of subperiodic Brugia malayi in the jird, Meriones unguiculatus, with notes on infections in other rodents. Journal of Parasitology 56, 969973.CrossRefGoogle ScholarPubMed
Chandrashekar, R., Rao, U.R. & Subrahmanyam, D. (1985) Serum dependent cell mediated immune reactions to Brugia pahangi infected larvae. Parasite Immunology 7, 633641.CrossRefGoogle Scholar
Chusattayanond, W. & Denham, D.A. (1984) Induction of host resistance to Brugia pahangi in jirds (Meriones unguiculatus) protected by chemoprophylaxis. Journal of Helminthology 58, 245249.CrossRefGoogle ScholarPubMed
Chusattayanond, W. & Denham, D.A. (1986) Attempted vaccination of jirds (Meriones unguiculatus) against Brugia pahangi with radiation attenuated infective larvae. Journal of Helminthology 60, 149155.CrossRefGoogle ScholarPubMed
Clark, l.A. & Howell, M.J. (1990) Protozoan parasites of erythrocytes and macrophages. pp. 146167 in Behnke, J.M. (Ed.) Immunity and pathology - the consequences of parasitic infection in mammals. London, Taylor & Francis.Google Scholar
Dean, D.A. (1983) Schistosoma and related genera: acquired resistance in mice. Experimental Parasitology 55, 1104.CrossRefGoogle ScholarPubMed
Denham, D.A., Suswillo, R.R. & Chusattayanond, W. (1984) Parasitological obsrevations on Meriones unguiculatus singly or multiply infected with Brugia pahangi. Parasitology 88, 295301.Google Scholar
Hamann, K.J., Gleich, G.J., Checkel, J.L., Loegering, D.A., McCall, J.W. & Barker, R.L. (1990) In vitro killing of microfilariae of Brugia pahangi and Brugia malayi by eosinophil granule proteins. Journal of Immunology 144, 31663173.Google Scholar
Hayashi, Y., Nogami, S., Nakamura, M., Shirasaka, A. & Noda, K. (1984) Passive transfer of protective immunity against Brugia malayi in BALB/c mice. Japanese Journal of Experimental Medicine 54, 183187.Google ScholarPubMed
Horii, Y., Nakanishi, H., Mori, A., Ueda, M., Kurokawa, K., Zaitsu, M., Oda, T. & Fujita, K. (1992) Induction of protective immunity to Brugia pahangi in jirds by drug-abbreviated infection. Journal of Helminthology 66, 147154.CrossRefGoogle ScholarPubMed
Ikeda, T. & Oikawa, Y. (1991) Paragonimus ohirai: immunobiochemical characterization on the tegumental glycocalyx of excysted juvenile recognised by a monoclonal antibody. Experimental Parasitology 72, 252261.CrossRefGoogle ScholarPubMed
Johnson, P., Mackenzie, C.D., Suswillo, R.R. & Denham, D.A. (1981) Serum mediated adherence of feline granulocyte to microfilariae of Brugia pahangi in vitro: variations with parasitic maturation. Parasite Immunology 3, 6980.Google Scholar
Klei, T.R., Enright, F.M., McDonough, K.C. & Coleman, S.U. (1988) Brugia pahangi: granulomatous lesion development in jirds following single and multiple infections. Experimental Parasitology 66, 132139.CrossRefGoogle ScholarPubMed
Lammie, P.J. & Katz, S.P. (1983a) Immunoregulation in experimental filariasis. I. In vitro supression of mitogen induced blastogenesis by adherent cells from jirds chronically infected with Brugia pahangi. Journal of Immunology 130, 13821385.Google Scholar
Lammie, P.J. & Katz, S.P. (1983b) Immunoregulation in experimental filariasis. II. Responses to parasite and nonparasite antigens in jirds with Brugia pahangi. Journal of Immunology 130, 13861389.CrossRefGoogle ScholarPubMed
Lammie, P.J. & Katz, S.P. (1984) Immunoregulation in experimental filariasis. III. Demonstration and characterization of antigenicspecific supressor cells in the spleen of Brugia pahangi-infected jirds. Immunology 52, 211219.Google Scholar
Lucius, R., Ruppel, A. & Diesfield, H.J. (1986) Dipetalonema vitae: resistance in Meriones unguiculatus with multiple infections of stage-3 larvae. Experimental Parasitology 62, 237246.CrossRefGoogle Scholar
Maruyama, H., Kobayashi, T., Tsuchiya, K., Horii, Y & Nawa, Y. (1994) Sensitive enzyme-linked immunosorbent assay (ELISA) method to measure parasite-specific antibodies of Mongolian gerbils. Japanese Journal of Parasitology 43,351357.Google Scholar
Nakanishi, H., Horii, Y., Fujita, K., Terashima, K., Ueda, M. & Kurokawa, K. (1987) Differences of eosinophil response among three species of rodents, rat, jird and mouse, during the course of Brugia pahangi infection. Tropical Medicine 29, 6164.Google Scholar
Yates, J.A. & Higashi, G.I. (1985) Brugia malayi: vaccination of jirds with 60cobalt-attenuated infective stage larvae protects against homologous challenge. American Journal of Tropical Medicine and Hygiene 34, 11321137.CrossRefGoogle ScholarPubMed
Yates, J.A. & Higashi, G.I. (1986) Ultrastructural observations on the fate of Brugia malayi injirds previously vaccinated with irradiated infective stage larvae. American Journal of Tropical Medicine and Hygiene 35, 982987.CrossRefGoogle ScholarPubMed