Inhibition of mucosal IgA and inflammatory response provoked by Trichinella spiralis during subsequent Heligmosomoides polygyrus infection in BALB/c mice

Acta Parasitologica

Volumn 46, Issue 2, 2001, Pages 138-147

  Doligalska, Maria ^a   Mijal, Joanna ^a   Laskowska, Marzena ^a  

^a UNIVERSITY OF WARSAW   (Poland)

Author keywords

Eosinophils; Heligmosomoides polygyrus; IL 5; Mast cells; sIgA; Trichinella spiralis

Indexed keywords

EID: 0346978025     PISSN: 12302821     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (49)

1. Abu-Ghazaleh R.I., Fujisawa T., Mestecky J., Kyle R.A., Gleich G.J. 1989. IgA-induced eosinophil degranulation. Journal of Immunology, 142, 2393-2400.
2. Beagley K.W., Eldridge J.H., Kiyono H., Everson M.P., Koopman W.J., Honjo T., McGhee J.R. 1988. Recombinant murine IL-5 induces high rate IgA synthesis in cycling IgA-positive Peyer's patch B cells. Journal of Immunology, 141, 2035-2042.
3. Behnke J.M., Cabaj W., Wakelin D. 1992. Susceptibility of adult Heligmosomoides polygyrus to intestinal inflammatory responses induced by heterologous infection. International Journal for Parasitology, 22, 75-86.
4. Behnke J.M., Wahid F.N., Grencis R.K., Else K.J., Ben-Smith A., Goyal P.K. 1993. Immunological relationships during primary infection with Heligmosomoides polygyrus (Nematospiroides dubius); down regulation of specific cytokine secretion (IL-9 and IL-10) correlates with poor mastocytosis and chronic survival of adult worms. Parasite Immunology, 15, 415-421.
5. Bell R.G. 1998. The generation and expression of immunity to Trichinella spiralis in laboratory rodents. Advances in Parasitology, 41, 149-217.
6. Bell R.G., McGreagor D.D., Despommier D.D. 1979. Trichinella spiralis: mediation of the intestinal component of protective immunity in the rat by multiple phase-specific antiparasitic responses. Experimental Parasitology, 47, 140-157.
7. Ben-Smith A., Wahid F.N., Lammas D.A., Behnke J.M. 1999. The relationship between circulating and intestinal Heligmosomoides polygyrus-specific IgG1 and IgA and resistance to primary infection. Parasite Immunology, 21, 383-395.
8. Campbell W.C. 1965. Immunizing effect of enteral and entero-parenteral infections of Trichinella spiralis in mice. Journal of Parasitology, 51, 185-194.
9. Coffman R.L., Lebman D.A., Shrader B. 1989a. Transforming growth factor beta specifically enhanced IgA production by lipopolysaccharide-stimulated murine B lymphocytes. Journal of Experimental Medicine, 170, 1039-1044.
10. Coffman R.L., Seymour B.W.P., Hudak S., Jackson J., Rennick D. 1989b. Antibody to interleukin-5 inhibits helminth-induced eosinophilia in mice. Science, 245, 308-310.
11. Dehlawi M.S., Wakelin D. 1988. Suppression of mucosal mastocytosis by Nematospiroides dubius results from an adult worm-mediated effect upon host lymphocytes. Parasite Immunology, 10, 85-95.
12. Dehlawi M.S., Wakelin D., Behnke J.M. 1987. Suppression of mucosal mastocytosis by infection with the intestinal nematode Nematospiroides dubius. Parasite Immunology, 9, 187-194.
13. De Vos T., Danell G., Dick T.A. 1992. Trichinella spiralis: dose dependence and kinetics of the mucosal immune responses in mice. Experimental Parasitology, 75, 99-111.
14. Doligalska M., Mijal J. 2000. IgG1 and IgG2a responses specific to Trichinella spiralis during subsequent infection with Heligmosomoides polygyrus in BALB/c mice. Acta Parasitologica, 45, 115-120.
15. Donaldson L.E, Schmitt E., Huntley J.F., Newlands G.F.J., Grencis R.K. 1996. A critical role for stem cell factor and c-kit in host protective immunity to an intestinal helminth. International Immunology, 8, 559-567.
16. Else K.J., Finkelman F.D. 1998. Intestinal nematode parasites, cytokines and effector mechanisms. International Journal for Parasitology, 28, 1145-1158.
17. Else K.J., Grencis R.K. 1991. Cellular immune response to murine nematode Trichuris muris. 1. Differential cytokine production during acute or chronic infection. Immunology, 11, 508-513.
18. Finkelman F.D., Shea-Donohue T., Goldhill J., Sullivan C.A., Morris S.C., Madden K.B., Gause W.C., Urban J.F.Jr. 1997. Cytokine regulation of host defence against parasitic gastrointestinal nematodes: Lessons from studies with rodent models. Annual Reviews in Immunology, 15, 505-533.
19. Furgal A., Litwin J. 1993. A simple method for demonstration of eosinophils in frozen sections. Folia Histochemica et Cytobiologica, 31, 197-199.
20. Grencis R.K. 1997. Th2-mediated host protective immunity to intestinal nematode infections. Philosophical Transactions of the Royal Society of London, B, 352, 1377-1384.
21. Grencis R.K., Hultner L., Else K.J. 1991. Host protective immunity to Trichinella spiralis in mice: activation of Th cell subsets and lymphokine secretion in mice expressing different response phenotypes. Immunology, 74, 329-332.
22. Hagan P., Wakelin D. 1982. Nematospiroides dubius: Effect of infection on lymphocyte responses to Trichinella spiralis in mice. Experimental Parasitology, 54, 157-165.
23. + lamina propria T-cell lines: phenotypic and functional characterization. Immunology, 75, 66-73.
24. Husband A.J., Kramer D.R., Bao S., Sutherland R.M., Beagley K.W. 1996. Regulation of mucosal IgA response in vivo: cytokines and adjuvants. Veterinary Immunology and Immunopathology, 54, 179-186.
25. Kopf M., Le Gros G., Bachmann M., Lamers M.C., Bluethmann H., Kohler G. 1993. Disruption of the murine IL-4 gene blocks Th2 cytokine responses. Nature, 362, 245-248.
26. Lin Y., Shockett P., Stavnezer J. 1991. Regulation of the antibody class switch to IgA. Immunology Research, 10, 376-380.
27. + T lymphocytes: effects of anti-L3T4 treatment on the gastrointestinal immune system. International Immunology, 3, 793-805.
28. Molinari J.A., Ebersole J.L., Cypess R.H. 1978. Specific antibody levels in the serum of Heliginosomoides polygyrus-infected mice. Journal of Parasitology, 64, 233-238.
29. Morton H.C., Van Egmond M., Van de Winkel J.G. 1996. Structure and function of human IgA Fc receptors (Fc alpha R). Critical Reviews in Immunology, 16, 423-440.
30. Murray P.D., McKenzie D.T., Swain S.L., Kaganoff M.F. 1987. Interleukin 5 and interleukin 4 produced by Peyer's patch T cells selectively enhance immunoglobulin A expression. Journal of Immunology, 139, 2669-2674.
31. + Th2 cells producing IL-6 and IL-10 are associated with mucosal immunoglobulin A responses. Infection and Immunity, 64, 1516-1525.
32. Pond L., Wassom D.L., Hayes C.E. 1989. Evidence for differential induction of helper T cell subsets during Trichinella spiralis infection. Journal of Immunology, 143, 4232-4237.
33. Pritchard D.I., Ali N.M.H., Behnke J.M. 1984a. Analysis of the mechanism of immunodepression following heterologous antigenic stimulation during concurrent infection with Nematospiroides dubius. Immunology, 51, 633-642.
34. Pritchard D.I., Behnke J.M., Williams D.J.L. 1984b. Primary infection sera and IgG1 do not block host-protective immunity to Nematospiroides dubius. Immunology, 51, 73-81.
35. Pritchard D.I., Williams D.J.L., Behnke J.M., Lee T.D.G. 1983. The role of IgG1 hypergammaglobulinemia in immunity to the gastrointestinal nematode Nematospiroides dubius. The immunochemical purification, antigen-specificity and in vivo anti-parasite effect of IgG1 from immune serum. Immunology, 49, 353-365.
36. Ramsay A.J., Leong K.H., Boyle D., Ruby J., Ramshaw L.A. 1994. Enhancement of mucosal IgA responses by interleukins 5 and 6 encoded in recombinant vaccine vectors. Reproduction, Fertility and Development, 6, 389-392.
37. Robinson M., Gustad T.R., Erickson M.R. 1997. Immunological interaction between Trichinella spiralis and Heligmosomoides polygyrus: Cross reactivity between muscle larvae and antibodies raised to unrelated antigens. International Journal for Parasitology, 27, 865-872.
38. Robinson M., Gustad T.R., Wei F.-Y., David C.S., Storey N. 1994. Adult worm homogenate of the nematode parasite Heligmosomoides polygyrus induces proliferation of native T lymphocytes without MHC restriction. Cellular Immunology, 158, 157-166.
39. Shi H.N., Koski K.G., Stevenson M., Scott M. 1997. Zinc deficiency and energy restriction modify immune responses in mice during both primary and challenge infection with Heligmosomoides polygyrus (Nematoda). Parasite Immunology, 19, 363-373.
40. Spalding D.M., Griffin J.A. 1986. Different pathways of differentiation of pre-B cell lines are induced by dendritic cells and T cell from different lymphoid tissues. Cell, 44, 507-512.
41. Svetic A., Madden K.B., Zhou X.D., Lu P., Katona I.M., Finkelman F.D., Urban J.F., Gause W.C. 1993. A primary intestinal helminthic infection rapidly induces a gut-associated elevation of Th2-associated cytokines and IL-3. Journal of Immunology, 150, 3434-3441.
42. Takahashi Y. 1997. Antigens of Trichinella spiralis. Parasitology Today, 13, 104-106.
43. + T cells regulate the IgE response and protective immunity in mice. Experimental Parasitology, 73, 500-511.
44. Urban J.F.Jr., Katona I.M., Paul W.E., Finkelman F.D. 1991b. Interleukin 4 is important in protective immunity to a gastrointestinal nematode infection in mice. Proceedings of the National Academy of Sciences, USA, 88, 5513-5517.
45. Vajdy M., Kosco-Vilbros M.H., Kopf M., Kohler G., Lycke N. 1995. Impaired mucosal immune responses in interleukin 4 targeted mice. Journal of Experimental Medicine, 181, 41-53.
46. Wahid F.N., Behnke J.M., Grencis R.K., Else K.J., Ben-Smith A.W. 1994. Immunological relationships during primary infection with Heligmosomoides polygyrus: Th2 cytokines and primary response phenotype. Parasitology, 108, 461-471.
47. Wakatsaki Y., Strober W. 1993. Effect of downregulation of germline transcripts on immunoglobulin A isotype differentiation. Journal of Experimental Medicine, 178, 129-138.
48. Wedi B., Raap U., Lewrick H., Kapp A. 1998. IL-4-induced apoptosis in peripheral blood eosinophils. Journal of Allergy and Clinical Immunology, 102, 1013-1020.
49. Yamamoto M., Fujihashi K., Beagley K.W., McGhee J.R., Kiyono H. 1993. Cytokine synthesis by intestinal intraepithelial lymphocytes. Both gamma/delta T cell receptor-positive and alpha/beta T cell receptor-positive T cells in the G1 phase of cell cycle produce IFN-gamma and IL-5. Journal of Immunology, 150, 106-114.