Home » Volumes » Volume 18 April/June 1985 » Imunidade humoral e celular em indivíduos curados de leishmaniose visceral

Imunidade humoral e celular em indivíduos curados de leishmaniose visceral

Roberto Badaró; Edgar M. Carvalho; Maria de La Glória Orge Orge; Rodolfo S. Teixeira; Heonir Rocha

DOI: 10.1590/S0037-86821985000200003


RESUMO

Foi realizada avaliação imunológica em 48 indivíduos com históriapregressa de leishmaniose visceral (L. V)eem seis pacientes durante a fase aguda da doença e após o tratamento. Títulos significativos de anticorpos determinados pela técnica de imunofluorescência e/ou ELISA foram observados em 32 (67%) dos 48 casos. A avaliação da resposta imune humoral e celular nos seis pacientes durante a fase ativa da doença demonstrou títulos elevados de anticorpos (média 9536 ± 7169) e resposta línfoproliferativa ausente (323 ± 24). Após o tratamento (3 e 6 meses) os títulos de anticorpos só caíram em três dos seis pacientes, ao passo que linfócitos passaram a responder “in vítro” a antígenos de leíshmânía (11909 ± 5637). Estes dados demonstram que os indivíduos que adquirem leishmaniose visceral não são geneticamente incapacitados de responder a antígeno de leíshmânía equea persistência de títulos elevados de anticorpos anos após o tratamento, sugere que o parasita permaneça no hospedeiro após a cura clínica da doença.

Palavras-chave: Leishmaniose visceral. Calazar. Sorologia. Imunidade celular. Imunidade humoral.


ABSTRACT

Immunological studies were done in 48 subjects with a past history of visceral leishmaniasis and in 6 patients during the active phase of the disease and shortly after treatment. Antibody titers determined by immunofluorescence antibody test (IFA) or ELISA were positive in 32 (67%) of the 48 persons that had visceral leishmaniasis in the past. The mean antibody titer by the IFA in the 6 patients with active visceral leishmaniasis was 9536 ± 7169 and thymidine uptake in the lymphocyte blastogenesis assay was 323 ± 24. After treatment (3 and 6 months) antibody titers had fallen only in 3 of the 6 patients and a restoration of the lymphocyte proliferative response wasobserved (11909 ±5637). These data demonstrated that there is no genetic inability of the host who acquire visceral leishmaniasis to develop a cellular immune response to leishmania antigen. Moreover, the longterm persistence of high antibody titers following therapy suggests that the parasite may stay in the host for long time even after apparent clinical cure of the infection.

Keywords: Leishmaniasis. Visceral leishmaniasis. Kala-azar. Humoral immunity. Cellular immunity.


 

 

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REFERÊNCIAS BIBLIOGRÁFICAS

1. Andrade TM, Teixeira R, Andrade JAF, Pereira C, Carvalho EM. Hipersensibilidade de tipo retardado na leishmaniose visceral. Revista do Instituto de Medicina Tropical de Sào Paulo 24: 298-302, 1982.         [ Links ]

2. Anthony R, CristensenHA, Johnson CM. Micro enzyme linked immunosorbent assay (ELISA) for serodiagnosis of new world leishmaniasis. The American Journal of Tropical Medicine and Hygiene 29: 190-194,1980.         [ Links ]

3. Badaró R, Orge MGO, Lorenço R, Teixeira R. ELISA na Leishmaniose Visceral Americana: Avaliação da sensibilidade e especificidade do teste. IX Reunião Anual de Pesquisa Básica em Doença de Chagas. Caxambu p. 44, 1982.         [ Links ]

4. Badaró R, Reed SG, Carvalho EM. Immunofluorescent antibody test in American Visceral Leishmaniasis: sensitivity and specificity of different morphological forms of two leishmania species. The American Journal of Tropical Medicine and Hygiene 32: 480-484, 1983.         [ Links ]

5. Bina JC, Prata A. An attempt to control schistosomiasis in an endemic area by the use of hycanthone as a chemotherapeutic agent. Revista da Sociedade Brasileira de Medicina Tropical 8: 217-224, 1974.         [ Links ]

6. Bryceson ADM, Turk JL. The effect of prolonged treatment with anti-lymphocyte serum on the course of infection with BCG and Leishmania enrietti in the guinea pig. The Journal of Pathology 104: 153-165, 1971.         [ Links ]

7. Camargo ME, Rebonato C. Cross reactivity inimmunofluorescence test for trypanosoma and leishmania anti- bodies. A simple inhibition procedure to ensure specific results. The American Journal of Tropical Medicine and Hygiene 18: 500-505, 1969.         [ Links ]

8. Camargo ME, Ferreira AE, Mineo JR, Takigute CK, Nakahara OS. Immunoglobulin G and immunoglobulin M enzyme-linked immunosorbent assay and defined toxoplasmosis serologic patterns. Infection and Immunity 21: 55-58, 1978.         [ Links ]

9. Carvalho EM, Teixeira RS, Johnson WD. Cell mediated immunity in American Visceral Leishmaniasis. Reversible immunosuppression during acute infection. Infection and Immunity 22: 649-656, 1981.         [ Links ]

10. Carvalho EM, Andrews BS, Martinelli R, Dutra M, Rocha H. Circulating immune complexes and rheumatoid factor in visceral leishmaniasis and schistosomiasis. The American Journal of Tropical Medicine and Hygiene 32: 61-68, 1983.         [ Links ]

11. Duxbury RE, Sadun EH. Fluorescent antibody test for the serodiagnosis of Visceral Leishmaniasis. The American Journal of Tropical Medicine and Hygiene 13: 525- 529, 1964.         [ Links ]

12. Haldar JP, Ghose S, Saha KC, Ghose AC. Cell mediated immune response in Indian Kala-azar and Post Kala- azar dermal leishmaniasis. Infection and Immunity 42: 702-707, 1983.         [ Links ]

13. Ho M. Leeuwenberg J, Mbugua G, Wamachi A, Voller A. An enzyme-linked immunosorbent assay (ELISA) for fteld diagnosis of Visceral Leishmaniasis. The American Journal of Tropical Medicine and Hygiene 32: 943- 946, 1983.         [ Links ]

14. Hommel M, Peters W, Ranque J, Duilirci M, Lonatte G. The micro-ELISA technique in the serodiagnosis of Visceral Leishmaniasis. Annals of Tropical Medicine and Parasitology 72: 213-218, 1978.         [ Links ]

15. Horwitz DA, Garret MA. Distinctive functional properties of human blood L lymphocytes. A comparison with T lymphocytes, B lymphocytes and monocytes. The Journal oflmmunology 118: 1712-1721, 1977.         [ Links ]

16. Howard JG, Hale G, Liew FY. Genetically determined response mechanisms to cutaneous leishmaniasis. The Transactions of the Royal Society of Tropical Medicine and Hygiene 76: 152-154, 1982.         [ Links ]

17. Jaffe CL, Grimaldi GJr, Bennet E, McMahon-Pratt D. Characterization of the New Worlds leishinania stocks by means of monoclonal antibodies. IV L. donovani complex. X Reunião Anual de Pesquisa Básica em Doença de Chagas, Caxambu p. 16, 1983.         [ Links ]

18. Jones TC, Yeh S, Hirsch JG. The interaction between Toxoplasma gondii and mammalian cells. I Mechanisms of entry and intracellular fate of the parasite. The Journal of Experimental Medicine 136: 1157-1172, 1972.         [ Links ]

19. Kharazmi A, Rezai HR Fani M, Behforrouz CC. Evidence for the presence of circulating immune complexes in serum and C3b and C3d on red cells of Kala- azar patients. The Transactions of the Royal Society of Tropical Medicine and Hygiene 76: 793-796, 1982.         [ Links ]

20. Lowry DH, Rosebrough MJ, Farr AL, Randall RJ. Protein measurement with folin phenol reagent. Journal ofBiological Chemistry 193: 265-275, 1951.         [ Links ]

21. Maguire JH, Mott KF, Hoff R, Guimarães A, Franca JT, Almeida de Souza JA, Ramos NB, Sherlock IA. A three year follow-up study of infection with Trypanosoma cruzi and eletrocardiografic abnormalities in a rural community in northeast Brazil. The American Journal of Tropical Medicine and Hygiene 31: 42-47, 1982.         [ Links ]

22. Murray HW, Masur H, Keithly JS. Cell mediated immune response in experimental visceral leishmaniasis. I. Correlation between resistance to Leishmania donovani and lymphokine generating capacity. The Journal of Immunology 129: 344-350, 1982.         [ Links ]

23. Naot Y, Remington JS. An Enzyme linked immunosorbent assay for detection of IgM antibodies to Toxoplasma gondii: Use for diagnosis of acute acquired toxoplasmosis. The Journal of Infectious Diseases 142:757-766, 1980.         [ Links ]

24. Preston PM, Carter RL, Leuchars E, Davies AJS, Dumonde DC. Experimental cutaneous leishmaniasis. III. Effects of thymectomy on the course of infection of CBA mice with Leishmania tropica. Clinical and Experimental Immunology 10: 337-357, 1972.         [ Links ]

25. Rezai HR, Behjorouz N, Amirhakimi G, Kohanteh J. Immunofluorescence and counter immuno eletrophoresis in the diagnosis of Kala-azar. The Transactions of the Royal Society of Tropical Medicine and Hygiene 71: 149-151, 1977.         [ Links ]

26. Rezai HR, Ardehali SM, Amirhakimi G, Kharazmi A. Immunological features of Kala-azar. The American Journal of Tropical Medicine and Hygiene 27: 1079- 1083, 1978.         [ Links ]

27. Rezai HR Farrel J, Solsby EL. Immunological response ofL. donovani infection in mice and significance of the T cell in resistance to experimental leishmaniasis. Clinical and Experimental Immunology 40: 508-514, 1980.         [ Links ]

28. Shaw JJ, Voller A. The detection of circulating antibody to Kala-azar by means of immunofluorescent techniques. The Transactions of the Royal Society of Tropical Medicine and Hygiene 58: 342-352, 1964.         [ Links ]

29. Sherlock IA, Almeida SP. Observações sobre calazar em Jacobina-1. Histórico e dados preliminares. Revista Brasileira de Malariologia e Doenças Tropicais 21:523- 534, 1969.         [ Links ]

30. Skow CB, Towhy DW. Cellular immunity to Leishmania donovani. II. Evidence for synergism between thymocytes and lymphocyte cells in reconstitution of acquired resistance to L. donovani in mice. The Journal of Immunology 113: 2012-2019, 1974.         [ Links ]

31. Teixeira R. Experiências vividas com a leishmaniose visceral 1954-1980 (Aspectos epidemiológicos, sorológicos e evolutivos). Tese para Professor Titular, Universidade Federal da Bahia, Salvador, 1980.         [ Links ]

 

 

 Endereço para correspondência:
Hospital Prof. Edgard Santos
Laboratório de Imunologia
40.000
Salvador – Bahia – Brasil.

 

 

Recebido para publicação em 24/10/84.

 

 

Trabalho realizado no Laboratório de Imunologia do Hospital Prof. Edgard Santos com o apoio do CNPq (nos 40.3685/82, 40.3695/82) e do National Institute of Health (nP AI 16282).