Literature DB >> 3179584

Visceral leishmaniasis: a disease associated with inability of lymphocytes to activate macrophages to kill leishmania.

E M Carvalho1, O A Bacellar, S Reed, A Barral, H Rocha.   

Abstract

1. The production of lymphokines capable of activating macrophages to kill leishmania was evaluated in seven visceral leishmaniasis patients. 2. Macrophages from healthy donors cultivated in vitro with supernatants from lymphocyte cultures of visceral leishmaniasis patients were infected with L. d. chagasi or L. m. amazonensis. After infection the number of amastigotes per 100 cells was counted. 3. The supernatant from visceral leishmaniasis lymphocytes did not significantly reduce the number of intracellular amastigotes of L. donovani chagasi (89 +/- 27%) in relation to controls (culture containing medium alone). In contrast, supernatants of mucocutaneous lymphocyte cultures decreased the percentage of infection to 26 +/- 11%. The supernatant of antigen-stimulated lymphocyte cultures from visceral leishmaniasis patients also did not inhibit L. mexicana amazonensis growth. The supernatant of visceral leishmaniasis lymphocytes stimulated with PHA reduced the number of intracellular amastigotes to 62 +/- 23% in relation to controls. 4. The inability of lymphocytes from visceral leishmaniasis patients to proliferate when stimulated with leishmania antigens and to activate macrophages to kill leishmania may represent a fundamental defect and lead to the acquisition of the disease.

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Year:  1988        PMID: 3179584

Source DB:  PubMed          Journal:  Braz J Med Biol Res        ISSN: 0100-879X            Impact factor:   2.590


  8 in total

1.  New challenges in the epidemiology and treatment of visceral leishmaniasis in periurban areas.

Authors:  Kathryn M Dupnik; Eliana L Nascimento; Joao F Rodrigues-Neto; Tatjana Keesen; Maria Zélia Fernandes; Iraci Duarte; Selma M B Jeronimo
Journal:  Drug Dev Res       Date:  2011-09       Impact factor: 4.360

2.  Functional and phenotypic changes in human lymphocytes after coincubation with Leishmania donovani in vitro.

Authors:  L Hviid; A L Sørensen; A Kharazmi; T G Theander
Journal:  Infect Immun       Date:  1990-10       Impact factor: 3.441

3.  Immune response measured in human volunteers vaccinated with autoclaved Leishmania major vaccine mixed with low dose of BCG.

Authors:  M Mahmoodi; A Khamesipour; Y Dowlati; S Rafati; A Z Momeni; M Emamjomeh; H Hejazi; F Modabber
Journal:  Clin Exp Immunol       Date:  2003-11       Impact factor: 4.330

4.  Differential effects of antigens from L. braziliensis isolates from disseminated and cutaneous leishmaniasis on in vitro cytokine production.

Authors:  Paulo T G Leopoldo; Paulo R L Machado; Roque P Almeida; Albert Schriefer; Angela Giudice; Amélia Ribeiro de Jesus; John L Ho; Luiz Henrique Guimarães; Olívia Bacellar; Edgar M Carvalho
Journal:  BMC Infect Dis       Date:  2006-04-25       Impact factor: 3.090

5.  Soluble CD40 Ligand in Sera of Subjects Exposed to Leishmania infantum Infection Reduces the Parasite Load in Macrophages.

Authors:  Fabrícia Alvisi de Oliveira; Aline Silva Barreto; Lays G S Bomfim; Talita Rebeca S Leite; Priscila Lima Dos Santos; Roque Pacheco de Almeida; Ângela Maria da Silva; Malcolm S Duthie; Steven G Reed; Tatiana Rodrigues de Moura; Amélia Ribeiro de Jesus
Journal:  PLoS One       Date:  2015-10-21       Impact factor: 3.240

6.  Transcriptional Profiling in Experimental Visceral Leishmaniasis Reveals a Broad Splenic Inflammatory Environment that Conditions Macrophages toward a Disease-Promoting Phenotype.

Authors:  Fanping Kong; Omar A Saldarriaga; Heidi Spratt; E Yaneth Osorio; Bruno L Travi; Bruce A Luxon; Peter C Melby
Journal:  PLoS Pathog       Date:  2017-01-31       Impact factor: 6.823

7.  Leishmania infantum (syn. L. chagasi) parasites affect the release of soluble CD14 by infected macrophages.

Authors:  Michelle Barreto Gomes Melo; Luana Celina Seraphim Cunha; Cárcia Santana Passos Barreto; Fabrícia Alvisi de Oliveira Mendonça; Micheli Luize Barbosa Santos; Danielle Sacramento; Amélia Ribeiro de Jesus; Roque Pacheco Almeida; Priscila Lima Dos Santos
Journal:  Parasitol Res       Date:  2021-08-05       Impact factor: 2.289

8.  High levels of soluble CD40 ligand and matrix metalloproteinase-9 in serum are associated with favorable clinical evolution in human visceral leishmaniasis.

Authors:  Fabrícia Alvisi de Oliveira; Carla Vanessa Oliveira Silva; Nayra Prata Damascena; Rodrigo Oliveira Passos; Malcolm S Duthie; Jeffrey A Guderian; Ajay Bhatia; Tatiana Rodrigues de Moura; Steven G Reed; Roque Pacheco de Almeida; Amélia Ribeiro de Jesus
Journal:  BMC Infect Dis       Date:  2013-07-19       Impact factor: 3.090

  8 in total

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