Apoptosis: A mechanism of immunoregulation during human schistosomiasis mansoni

Parasite Immunology

Volumn 22, Issue 6, 2000, Pages 267-277

  Carneiro Santos, Patricia ^a,b,e   Martins Filho, Olindo ^b   Alves Oliveira, Lucia F ^c   Silveira, Alda M S ^a,c   Coura Filho, Pedro ^b   Viana, Iramaya R C ^b   Wilson, Robert A ^d   Correa Oliveira, Rodrigo ^a,b  

^a FEDERAL UNIVERSITY OF MINAS GERAIS   (Brazil)

^b INSTITUTO OSWALDO CRUZ   (Brazil)

^c UNIVERSIDADE VALE DO RIO DOCE   (Brazil)

^d UNIVERSITY OF YORK   (United Kingdom)

^e UNIVERSITY OF GLASGOW   (United Kingdom)

Author keywords

Apoptosis; Human schistosomiasis mansoni; Soluble egg antigen; Soluble lung antigen preparation

Indexed keywords

ANTIGEN; CYTOKINE;

ADOLESCENT; ADULT; AGED; APOPTOSIS; ARTICLE; CELL POPULATION; CLINICAL ARTICLE; CLINICAL FEATURE; EGG; ENTEROPATHY; FEMALE; FLOW CYTOMETRY; HEPATOMEGALY; HEPATOSPLENOMEGALY; HUMAN; HUMAN CELL; IMMUNOREGULATION; MALE; PORTAL HYPERTENSION; PRIORITY JOURNAL; SCHISTOSOMA MANSONI; SCHISTOSOMIASIS; SCHOOL CHILD; T LYMPHOCYTE; WORM;

ADOLESCENT; ADULT; AGED; ANIMALS; ANTIGENS, HELMINTH; APOPTOSIS; B-LYMPHOCYTES; CELLS, CULTURED; CHILD; CYTOKINES; FECES; FEMALE; HUMANS; LEUKOCYTES, MONONUCLEAR; MALE; MIDDLE AGED; SCHISTOSOMA MANSONI; SCHISTOSOMIASIS MANSONI; T-LYMPHOCYTE SUBSETS;

SCHISTOSOMA MANSONI; SCHISTOSOMIASIS MANSONI; TREMATODA;

EID: 0034112342     PISSN: 01419838     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-3024.2000.00294.x     Document Type: Article

References (42)

1. Ameisen J.C., Estaquier J. & Idziorek T. (1994) From AIDS to parasite infection: pathogen-mediated subversion of programmed cell death as a mechanism for immune dysregulation. Immunological Reviews 142, 9-51
2. Boros D.L. (1989) Immunopathology of Schistosoma mansoni infection. Clinical Microbiological Review 2, 250-269
3. Coligan J.E., Kruisbeek A.M., Margulies D.H. et al. (1995). Common Immunologic techniques. In Current Protocols in Immunology
4. Colley D.G., Cook J.A., Freeman G.L. et al. (1977) Immune responses during human schistosomiasis mansoni. I. In vitro lymphocyte blastogenic responses to heterogeneous antigen preparations from schistosome eggs, worms and cercariae. International Archives of Allergy and Applied Immunology 53, 420-433
5. Colley D.G., Garcia A.A., Lambertucci J.R. et al. (1986) Immune responses during human schistosomiasis XII. Differential responsiveness in patients with hepatosplenic disease. American Journal of Tropical Medicine and Hygiene 35, 793-802
6. Colley D.G., Lewis F.A. & Todd C.W. (1979) Adoptive suppression of granuloma formation by T lymphocytes and by cells sensitive to cyclophosphamide. Cell Immunology 46, 192-200
7. Del Prete G., De Carli M., Almerigogna F. et al. (1993) Human IL-10 is produced by both type 1 helper (Th1) and type 2 helper (Th2) T cell clones and inhibits their antigen-specific proliferation and cytokine production. Journal of Immunology 150, 353-360
8. Ding L., Linsley P.S., Huang L.Y., Germain R.N. & Shevach M. (1993) IL-10 inhibits macrophage costimulatory activity by selectively inhibiting the up-regulation of B7 expression. Journal of Immunology 151, 1224-1234
9. Doughty B.L., Goes A.M., Parra J.C. et al. (1989) Anti-idiotypic T cells in human schistosomiasis. Immunological Investigations 18, 373-388
10. Estaquier J., Marguerite M., Sahuc F. et al. (1997) Interleukin-10-mediated T cell apoptosis during the T helper type 2 cytokine response in murine Schistosoma mansoni parasite infection. European Cytokine Network 8, 153-160
11. Falcao P.L., Malaquias L.C., Martins-Filho O.A. et al. (1998) Human schistosomiasis mansoni: IL-10 modulates the in vitro granuloma formation. Parasite Immunology 20, 447-454
12. Fiorentino D.F., Zlotinik A., Vieira P. et al. (1991) IL-10 acts on the antigen-presenting cell to inhibit cytokine production by Th1 cells. Journal of Immunology 146, 3444-3451
13. Flores Villanueva P.O., Chikunguwo S.M., Harris T.S. et al. (1993) Role of IL-10 on antigen-presenting cell function for schistosomal egg-specific monoclonal T helper cell responses in vitro and in vivo. Journal of Immunology 151, 3192-3198
14. Fraker P.M., King L.E., Lill-Elghanian D. et al. (1995) Quantification of apototic events in pure and heterogeneous populations of cells using the flow cytometer. Methods in Cell Biology 46, 57-76
15. Gazzinelli G. & Colley D.G. (1992) Human immune responses during schistosomiasis mansoni. Reviews of Society of Brasileira Medicine Tropical 25, 125-134
16. Gazzinelli G., Katz N., Rocha R.S. & Colley D.G. (1983) Immune response during human schistosomiasis mansoni X. Production and standartization of an antigen-induced mitogenic activity by peripheral blood mononuclear cells from treated but not active cases of schistosomiasis. Journal of Immunology 130, 2891-2895
17. Gazzinelli G., Lambertucci J.R. & Katz N. (1985) Immune response during human schistosomiasis. XI. Immunologic status of patients with acute infections and after treatment. Journal of Immunology 135, 2121-2126
18. Gazzinelli G., Montesano M.A., Correa-Oliveira R. et al. (1987) Immune response in different clinical groups of schistosomiasis patients. Memoires of the Institute Oswaldo Cruz 82, 95-100
19. Goes A.M., Rezende S.A., Gazzinelli G. & Doughty B.L. (1994) Granulomatous hypersensitivity to Schistosoma mansoni egg antigens in human schistosomiasis. IV. A role for prostaglandin-induced inhibition of in vitro granuloma formation. Parasite Immunology 16, 11-18
20. Goes A.M., Rocha R.S., Gazzinelli G. & Doughty B.L. (1989) Production and characterization of human monoclonal antibodies against Schistosoma mansoni. Parasite Immunology 11, 695-711
21. Hernandez H.J., Wang Y. & Stadecker M.J. (1997) In infection with Schistosoma mansoni, B cells are required for T helper type 2 cell responses but not for granuloma formation. Journal of Immunology 158, 4832-4837
22. + cell-mediated granulomatous pathology in schistosomiasis is downregulated by a B cell-dependent mechanism requiring Fc receptor signaling. Journal of Experimental Medicine 187, 619-629
23. Katz N., Chaves A. & Pellegrino J. (1972) A single device for quantitative stool thick smear technique in schistosomiasis mansoni. Revista Do Instituto de Medicina Tropical de Sao Paulo 14, 397-400
24. + T cell death by apoptosis in experimental Chagas' disease. Journal of Immunology 154, 744-752
25. Lowry O.H., Rosebrough N.J., Farr A.L. et al. (1951) Protein measurement with the Folin phenol reagent. Journal of Biological Chemistry 193, 265-275
26. Malaquias L.C.C., Falcao-Valença P., Silveira A.M.S. et al. (1997) Cytokine regulation of human response to Schistosama mansoni: I. Analysis of the role of IL-4, 5, 10 on the peripheral blood mononuclear cells responses. Scandinavian Journal of Immunology 46, 393-398
27. Martins-Filho O.A., Dutra W.O., Freeman G.L. et al. (1997) Flow cytometric study of blood leukocytes in clinical forms of human schistosomiasis. Scandinavian Journal of Immunology 46, 304-311
28. Montesano M.A., Lima M.S., Correa-Oliveira R. et al. (1989) Immune responses during human schistosomiasis mansoni XVI. Idiotypic differences in antibody preparations from patients with different clinical forms offection. Journal of Immunology 142, 2501-2506
29. Mountford A.P., Harrop R. & Wilson R.A. (1995) Antigens derived from lung-stage larvae of Schistosoma mansoni are efficient stimulators of proliferation and gama interferon secretion by lymphocytes from mice vaccinated with attenuated larvae. Infection and Immunity 63, 1980-1986
30. Nicoletti I., Migliorati G., Pagliacci M.C. et al. (1991) A rapid and simple method for measuring thymocyte apoptosis by propidium iodide staining and flow cytometry. Journal of Immunological Methods 139, 271-279
31. O'Brien M.C. & Bolton W.E. (1995) Comparison of cell viability probes compatible with fixation and permeabilization for combined surface and intracellular staining in flow cytometry. Cytometry 19, 243-255
32. Ottesen E.A. (1979) Modulation of the host immune response in human schistosomiasis I. Adherent suppressor cells that inhibit lymphocytes proliferative responses to parasite antigens. Journal of Immunology 123, 1639-1645
33. Parra J.C., Gazzinelli G., Goes A.M. et al. (1991) Granulomatous hypersensivity to Schistosoma mansoni egg antigens in human schistosomiasis II. In vitro granuloma modulation induced by polyclonal idiotypic antibodies. Journal of Immunology 147, 3949-3954
34. Parra J.C., Lima M.C., Gazzinelli G. et al. (1988) Immune responses during human schistosomiasis mansoni XV. Anti-idiotypic T cells can recognize and respond to anti-SEA idiotypes directly. Journal of Immunology 140, 2401-2405
35. Pedras-Vasconcelos J.A. & Pearce E.J. (1996) Type 1, CD8+ T cell responses during infection with the helminth Schistosoma mansoni. Journal of Immunology 157, 3046-3053
36. Ramalho-Pinto F.J., Gazzinelli G., Howells R.E. et al. (1974) Schistosoma mansoni: defined system for stepwise transformation of cercariae to schistosoma in vitro. Experimental Parasitology 36, 360
37. Rocklin R.E., Brown A.P., Warren K.S. et al. (1980) Factors that modify the cellular-immune response in patients infected by Schistosoma mansoni. Journal of Immunology 125, 1916-1923
38. Salgame P., Abrams J.S., Clayberger C. et al. (1991) Differing lymphokine profiles of functional subsets of human CD4 and CD8 T cell clones. Science 254, 279-282
39. Samuelson J.C., Caulfield J.P. & David J.R. (1980) Schistosoma mansoni: post-transformational surface changes in schistosomula grown in vitro and in mice. Experimental Parasitology 50, 369-383
40. Todd C., Goodgame R.W. & Colley D.G. (1979) Immune responses during human schistosomiasis mansoni V. Suppression of schistosomiasis antigen specific lymphocyte blastogenesis by adherent/phagocytic cells. Journal of Immunology 122, 1440-1446
41. Velupillai P. & Harn D.A. (1994) Oligosaccharide-specific induction of interleukin 10 production by B220+ cells from schistosome-infected mice: a mechanism for regulation of CD4+ T-cell subsets. Proceedings of the National Academy of Sciences of the USA 91, 18-22
42. World Health Organization. (1992). Progress in Research-Tropical Diseases. WHO, Geneva