Hostname: page-component-586b7cd67f-dlnhk Total loading time: 0 Render date: 2024-11-22T23:42:13.042Z Has data issue: false hasContentIssue false

Lymphoreticular responses to metacestodes: Taenia multiceps (Cestoda) can modify interaction between accessory cells and responder cells during lymphocyte activation

Published online by Cambridge University Press:  06 April 2009

N. K. Rakha
Affiliation:
Departments of Veterinary Pathology, University of Liverpool, P.O. Box 147, Liverpool L69 3BX
J. B. Dixon
Affiliation:
Departments of Veterinary Pathology, University of Liverpool, P.O. Box 147, Liverpool L69 3BX
G. C. Skerritt
Affiliation:
Veterinary Preclinical Sciences, University of Liverpool, P.O. Box 147, Liverpool L69 3BX
S. D. Carter
Affiliation:
Departments of Veterinary Pathology, University of Liverpool, P.O. Box 147, Liverpool L69 3BX
P. Jenkins
Affiliation:
Departments of Veterinary Pathology, University of Liverpool, P.O. Box 147, Liverpool L69 3BX
S. Marshall-Clarke
Affiliation:
Human Anatomy and Cell Biology, University of Liverpool, P.O. Box 147, Liverpool L69 3BX

Summary

This study was designed to test the accessory function of macrophages after activation with products of Taenia multiceps coenuri. Activation was carried out by intraperitoneal injection of mice with coenurus fluid or protoscolex culture supernatant, and function was assessed by adding these macrophages in progressively increasing numbers to macrophage-depleted lymphocyte cultures transforming under the influence of plant mitogens or coenurus-fluid mitogen. In contrast to normal macrophages, which have a progressively enhancing action on the above reactions, parasite-activated macro-phages at similar concentrations were progressively inhibitory. However, low concentrations of the activated macrophages enhanced mitosis as well as, or better than, normal. Lymph node cells from injected mice showed abnormal response to macrophage-derived signals. In particular there was subnormal reaction to macrophages in the presence of coenurus mitogen. These results suggest that T. multiceps coenuri may survive in the host because of their ability to reduce effective interaction between lymphocytes and accessory cells.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1991

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Ali-KHAN, Z. (1978). Pathological changes in the lymphoreticular tissues of Swiss mice infected with Echinococcus granulosus cysts. Zeitschrift für Parasitenkunde 58, 4754.CrossRefGoogle ScholarPubMed
Allan, D., Jenkins, P., Connor, R. J. & Dixon, J. B. (1981). A study of immunoregulation of Balb/c mice by Echinococcus granulosus equinus during prolonged infection. Parasite Immunology 3, 137–42.CrossRefGoogle ScholarPubMed
Cox, D. A., Dixon, J. B. & Marshall-Clarke, S. (1986). Transformation induced by Echinococcus granulosus protoscoleces in unprimed mouse spleen cells: identity and MHC restriction of participating cell types. Immunology 57, 461–6.Google ScholarPubMed
Dixon, J. B., Jenkins, P. & Allan, D. (1982). Immune recognition of Echinococcus granulosus. 1. Parasite-activated, primary transformation by normal murine lymph node cells. Parasite Immunology 4, 3345.CrossRefGoogle ScholarPubMed
Jenkins, P., Dixon, J. B., Rakha, N. K. & Carter, S. D. (1990). Regulation of macrophage-mediated larvicidal activity in Echinococcus granulosus and Mesocestoides corti (Cestoda) infection in mice. Parasitology 100, 309–15.CrossRefGoogle ScholarPubMed
Judson, D. G., Dixon, J. B., Clarkson, M. J. & Pritchard, J. (1985). Ovine hydatidosis: some immunological characteristics of the seronegative host. Parasitology 91, 349–57.CrossRefGoogle ScholarPubMed
Judson, D. G., Dixon, J. B. & Skerritt, G. C. (1987). Occurrence and biochemical characteristics of cestode lymphocyte mitogens. Parasitology 94, 151–60.CrossRefGoogle ScholarPubMed
Judson, D. G., Dixon, J. B., Skerritt, G. C. & Stallbaumer, M. (1984). Mitogenic effect of Coenurus cerebralis cyst fluid. Research in Veterinary Science 37, 128.CrossRefGoogle ScholarPubMed
Miller, B. M., Staugaitis, S. M., Tourtellotte, W. W., Shapshak, P., Goldberg., M., Heiner, D. & Weil, M. (1985). Intra-blood-brain barrier IgG synthesis in cerebral cysticercosis. Archives of Neurology 42, 782–4.CrossRefGoogle ScholarPubMed
Osada, T., Noro, N., Kuroda, Y. & Ikai, A. (1987). Murine T-cell proliferation can be specifically augmented by macrophages fed with specific antigen: alpha-2-macroglobulin conjugate. Biochemical and Biophysical Research Communications 146, 2631.CrossRefGoogle ScholarPubMed
Riley, E. M. & Dixon, J. B. (1987). Experimental Echinococcus granulosus infection in mice: immunocytochemical analysis of lymphocyte populations in local lymphoid organs during early infection. Parasitology 94, 523–32.CrossRefGoogle Scholar
Riley, E. M., Dixon, J. B., Kelly, D. F. & Cox, D. A. (1985). The immune response to Echinococcus granulosus: sequential histological observations of lymphoreticular and connective tissues during early murine infection. Journal of Comparative Pathology 95, 93100.CrossRefGoogle ScholarPubMed
Ross, G., Dixon, J. B. & Veevers, A. (1987). Variation in the lymphocyte transformation assay: slope analysis of cell dose–response curves. Journal of Immunological Methods 98, 189193.CrossRefGoogle ScholarPubMed
Skerritt, G. C. & Stallbaumer, M. F. (1984). Diagnosis and treatment of coenurosis (gid) in sheep. Veterinary Record 115, 399403.CrossRefGoogle Scholar