Abstract
Parasite-specific humoral and cell-mediated immune responses were investigated in highly susceptible (AKR and C57B1/6J) and relatively resistant (C57B1/10) mice undergoing secondary alveolar echinococcosis (infection with Echinococcus multilocularis metacestode). The parasite-specific proliferative immune response of lymph node cells upon in vitro antigen stimulation remained weak in all three mouse strains. By day 30 p.i., CD4+ lymphoblast cells dominated the total population of blast cells in all three mouse strains. There was, however, an unexpectedly high proportion of CD8+ blast cells; by day 90 p.i., a marked proportional increase in CD8+ cells was seen in susceptible (AKR and C57B1/6J), but not in resistant (C57B1/10) mice. Susceptible, but not resistant mice exhibited a significantly decreased responsiveness of lymph node cells to concanavalin A (Con A) stimulation on day 90 p.i. Analysis of the humoral immune response by ELISA showed that resistance in C57B1/10 mice was associated with the ability of the host to synthesize antibodies to Em2 of the IgG3 and IgG1 isotype. Em2 is a lectin-binding carbohydrate antigen of the laminated layer. In susceptible AKR and C57B1/6J mice, low levels of anti-Em2 antibodies of the IgG2a isotype were detected. Anti-Em2 antibodies of the IgG3/IgG1 isotype, however, were absent. Differences in subclass-specific IgG responses were confirmed by immunoblot analyses. Our findings suggest that differences in antigen recognition (with respect to subsets of humoral and cellular immune components), probably controlled by non-H-2 gene(s), coupled to immune suppression modulated by CD8+ cells and/or respective cytokines, may determine susceptibility or resistance in experimental infection with E. multilocularis.
Full text
PDF







Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bresson-Hadni S., Liance M., Meyer J. P., Houin R., Bresson J. L., Vuitton D. A. Cellular immunity in experimental Echinococcus multilocularis infection. II. Sequential and comparative phenotypic study of the periparasitic mononuclear cells in resistant and sensitive mice. Clin Exp Immunol. 1990 Nov;82(2):378–383. doi: 10.1111/j.1365-2249.1990.tb05457.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bresson-Hadni S., Vuitton D. A., Lenys D., Liance M., Racadot E., Miguet J. P. Cellular immune response in Echinococcus multilocularis infection in humans. I. Lymphocyte reactivity to Echinococcus antigens in patients with alveolar echinococcosis. Clin Exp Immunol. 1989 Oct;78(1):61–66. [PMC free article] [PubMed] [Google Scholar]
- Callard R. E., Turner M. W. Cytokines and Ig switching: evolutionary divergence between mice and humans. Immunol Today. 1990 Jun;11(6):200–203. doi: 10.1016/0167-5699(90)90082-k. [DOI] [PubMed] [Google Scholar]
- Dao M. L. An improved method of antigen detection on nitrocellulose: in situ staining of alkaline phosphatase conjugated antibody. J Immunol Methods. 1985 Oct 10;82(2):225–231. doi: 10.1016/0022-1759(85)90354-0. [DOI] [PubMed] [Google Scholar]
- Deplazes P., Gottstein B. A monoclonal antibody against Echinococcus multilocularis Em2 antigen. Parasitology. 1991 Aug;103(Pt 1):41–49. doi: 10.1017/s0031182000059278. [DOI] [PubMed] [Google Scholar]
- Eckert J., Pohlenz J. Zur Wirkung von Mebendazol auf Metazestoden von Mesocestoides corti und Echinococcus multilocularis. Tropenmed Parasitol. 1976 Sep;27(3):247–262. [PubMed] [Google Scholar]
- Gottstein B., Deplazes P., Aubert M. Echinococcus multilocularis: immunological study on the "Em2-positive" laminated layer during in vitro and in vivo post-oncospheral and larval development. Parasitol Res. 1992;78(4):291–297. doi: 10.1007/BF00937086. [DOI] [PubMed] [Google Scholar]
- Gottstein B., Eckert J., Fey H. Serological differentiation between Echinococcus granulosus and E. multilocularis infections in man. Z Parasitenkd. 1983;69(3):347–356. doi: 10.1007/BF00927876. [DOI] [PubMed] [Google Scholar]
- Gottstein B., Eckert J., Woodtli W. Determination of parasite-specific immunoglobulins using the ELISA in patients with echinococcosis treated with mebendazole. Z Parasitenkd. 1984;70(3):385–389. doi: 10.1007/BF00927825. [DOI] [PubMed] [Google Scholar]
- Gottstein B., Jacquier P., Bresson-Hadni S., Eckert J. Improved primary immunodiagnosis of alveolar echinococcosis in humans by an enzyme-linked immunosorbent assay using the Em2plus antigen. J Clin Microbiol. 1993 Feb;31(2):373–376. doi: 10.1128/jcm.31.2.373-376.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gottstein B., Mesarina B., Tanner I., Ammann R. W., Wilson J. F., Eckert J., Lanier A. Specific cellular and humoral immune responses in patients with different long-term courses of alveolar echinococcosis (infection with Echinococcus multilocularis). Am J Trop Med Hyg. 1991 Dec;45(6):734–742. doi: 10.4269/ajtmh.1991.45.734. [DOI] [PubMed] [Google Scholar]
- Gottstein B., Müller N., Cryz S. J., Jr, Vogel M., Tanner I., Seebeck T. Humoral and cellular immune response in mice and dogs induced by a recombinant Echinococcus multilocularis antigen produced by a Salmonella typhimurium vaccine strain. Parasite Immunol. 1990 Mar;12(2):163–174. doi: 10.1111/j.1365-3024.1990.tb00945.x. [DOI] [PubMed] [Google Scholar]
- Gottstein B., Müller N., Cryz S. J., Jr, Vogel M., Tanner I., Seebeck T. Humoral and cellular immune response in mice and dogs induced by a recombinant Echinococcus multilocularis antigen produced by a Salmonella typhimurium vaccine strain. Parasite Immunol. 1990 Mar;12(2):163–174. doi: 10.1111/j.1365-3024.1990.tb00945.x. [DOI] [PubMed] [Google Scholar]
- Gottstein B., Nash T. E. Antigenic variation in Giardia lamblia: infection of congenitally athymic nude and scid mice. Parasite Immunol. 1991 Nov;13(6):649–659. doi: 10.1111/j.1365-3024.1991.tb00560.x. [DOI] [PubMed] [Google Scholar]
- Gottstein B. Purification and characterization of a specific antigen from Echinococcus multilocularis. Parasite Immunol. 1985 May;7(3):201–212. doi: 10.1111/j.1365-3024.1985.tb00070.x. [DOI] [PubMed] [Google Scholar]
- Gottstein B., Tsang V. C., Schantz P. M. Demonstration of species-specific and cross-reactive components of Taenia solium metacestode antigens. Am J Trop Med Hyg. 1986 Mar;35(2):308–313. doi: 10.4269/ajtmh.1986.35.308. [DOI] [PubMed] [Google Scholar]
- Gottstein B., Tschudi K., Eckert J., Ammann R. Em2-ELISA for the follow-up of alveolar echinococcosis after complete surgical resection of liver lesions. Trans R Soc Trop Med Hyg. 1989 May-Jun;83(3):389–393. doi: 10.1016/0035-9203(89)90512-9. [DOI] [PubMed] [Google Scholar]
- Kilejian A., Schwabe C. W. Studies on the polysaccharides of the Echinococcus granulosus cyst, with observations on a possible mechanism for laminated membrane formation. Comp Biochem Physiol B. 1971 Sep 15;40(1):25–36. doi: 10.1016/0305-0491(71)90058-7. [DOI] [PubMed] [Google Scholar]
- Kizaki T., Ishige M., Bingyan W., Kumagai M., Day N. K., Good R. A., Onoé K. Interleukin-1-dependent mitogenic responses induced by protoscoleces of Echinococcus multilocularis in murine lymphocytes. J Leukoc Biol. 1993 Mar;53(3):233–239. doi: 10.1002/jlb.53.3.233. [DOI] [PubMed] [Google Scholar]
- Kizaki T., Kobayashi S., Ogasawara K., Day N. K., Good R. A., Onoé K. Immune suppression induced by protoscoleces of Echinococcus multilocularis in mice. Evidence for the presence of CD8dull suppressor cells in spleens of mice intraperitoneally infected with E. multilocularis. J Immunol. 1991 Sep 1;147(5):1659–1666. [PubMed] [Google Scholar]
- Kroeze W. K., Tanner C. E. Echinococcus multilocularis: susceptibility and responses to infection in inbred mice. Int J Parasitol. 1987 Apr;17(4):873–883. doi: 10.1016/0020-7519(87)90003-8. [DOI] [PubMed] [Google Scholar]
- Lanier A. P., Trujillo D. E., Schantz P. M., Wilson J. F., Gottstein B., McMahon B. J. Comparison of serologic tests for the diagnosis and follow-up of alveolar hydatid disease. Am J Trop Med Hyg. 1987 Nov;37(3):609–615. doi: 10.4269/ajtmh.1987.37.609. [DOI] [PubMed] [Google Scholar]
- Liance M., Bresson-Hadni S., Meyer J. P., Houin R., Vuitton D. A. Cellular immunity in experimental Echinococcus multilocularis infection. I. Sequential and comparative study of specific in vivo delayed-type hypersensitivity against E. multilocularis antigens in resistant and sensitive mice. Clin Exp Immunol. 1990 Nov;82(2):373–377. doi: 10.1111/j.1365-2249.1990.tb05456.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Liance M., Vuitton D. A., Guerret-Stocker S., Carbillet J. P., Grimaud J. A., Houin R. Experimental alveolar echinococcosis. Suitability of a murine model of intrahepatic infection by Echinococcus multilocularis for immunological studies. Experientia. 1984 Dec 15;40(12):1436–1439. doi: 10.1007/BF01951932. [DOI] [PubMed] [Google Scholar]
- Playford M. C., Ooi H. K., Ito M., Kamiya M. Lymphocyte engraftment conveys immunity and alters parasite development in scid mice infected with Echinococcus multilocularis. Parasitol Res. 1993;79(4):261–268. doi: 10.1007/BF00932179. [DOI] [PubMed] [Google Scholar]
- Rakha N. K., Dixon J. B., Carter S. D., Craig P. S., Jenkins P., Folkard S. Echinococcus multilocularis antigens modify accessory cell function of macrophages. Immunology. 1991 Dec;74(4):652–656. [PMC free article] [PubMed] [Google Scholar]
- Rausch R. L., Wilson J. F., Schantz P. M., McMahon B. J. Spontaneous death of Echinococcus multilocularis: cases diagnosed serologically (by Em2 ELISA) and clinical significance. Am J Trop Med Hyg. 1987 May;36(3):576–585. doi: 10.4269/ajtmh.1987.36.576. [DOI] [PubMed] [Google Scholar]
- Vuitton D. A., Bresson-Hadni S., Laroche L., Kaiserlian D., Guerret-Stocker S., Bresson J. L., Gillet M. Cellular immune response in Echinococcus multilocularis infection in humans. II. Natural killer cell activity and cell subpopulations in the blood and in the periparasitic granuloma of patients with alveolar echinococcosis. Clin Exp Immunol. 1989 Oct;78(1):67–74. [PMC free article] [PubMed] [Google Scholar]


