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Characterization of human infection by Leishmania spp. in the Northwest of Argentina: immune response, double infection with Trypanosoma cruzi and species of Leishmania involved

Published online by Cambridge University Press:  17 February 2003

F. M. FRANK
Affiliation:
Cátedra de Inmunología, Instituto de Estudios de la Inmunidad Humoral (IDEHU), CONICET-UBA, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín 956 4to P, 1113 Buenos Aires, Argentina
M. M. FERNÁNDEZ
Affiliation:
Cátedra de Inmunología, Instituto de Estudios de la Inmunidad Humoral (IDEHU), CONICET-UBA, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín 956 4to P, 1113 Buenos Aires, Argentina
N. J. TARANTO
Affiliation:
Laboratorio de Enfermedades Tropicales, Cátedra de Microbiología y Parasitología, Sede Regional Orán, Universidad Nacional de Salta, Argentina
S. P. CAJAL
Affiliation:
Laboratorio de Enfermedades Tropicales, Cátedra de Microbiología y Parasitología, Sede Regional Orán, Universidad Nacional de Salta, Argentina
R. A. MARGNI
Affiliation:
Cátedra de Inmunología, Instituto de Estudios de la Inmunidad Humoral (IDEHU), CONICET-UBA, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín 956 4to P, 1113 Buenos Aires, Argentina
E. CASTRO
Affiliation:
Laboratório de Parasitologia Molecular, Setor de Ciências Biológicas, Universidade Federal de Paraná, Brasil
V. THOMAZ-SOCCOL
Affiliation:
Laboratório de Parasitologia Molecular, Setor de Ciências Biológicas, Universidade Federal de Paraná, Brasil
E. L. MALCHIODI
Affiliation:
Cátedra de Inmunología, Instituto de Estudios de la Inmunidad Humoral (IDEHU), CONICET-UBA, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín 956 4to P, 1113 Buenos Aires, Argentina

Abstract

The aims of this study were to characterize human American tegumentary leishmaniasis, which includes cutaneous, mucocutaneous and mucosal leishmaniasis, in Northwest Argentina, to determine the prevalence of double infection with Trypanosoma cruzi and to identify the species of Leishmania in this area. Most of the 330 leishmaniasis patients presented cutaneous ulcers (96·1%), 2·4% mucocutaneous and 1·5% the mucosal form (‘espundia’). The aetiological agents, determined by isoenzyme electrophoresis, were identified as Leishmania (Viannia) braziliensis in 16 out of 20 isolates and in the remaining 4 as Leishmania (Leishmania) amazonensis, the first ever-documented in Argentina. Sera analysed by ELISA and IFA using complex antigen from both T. cruzi and L. braziliensis showed a very high percentage of positives (66·3–78·2%). When antigens for specific diagnosis of Chagas' disease were used, 40·9% of the leishmaniasis patients were also found to be infected by T. cruzi. These results indicate that the strong immune response against T. cruzi gave no protection to Leishmania, in spite of the serological cross-reaction between these parasites. In addition, we showed that more than 40% of the patients would be misdiagnosed as chagasic if complex antigens, as epimastigotes or soluble fraction from epimastigotes, were used in IFA or ELISA. This is of paramount importance not only because patients' treatment would be associated to misdiagnosis but the fact that in many countries in Central and South America, a positive test for Chagas' disease means a rejection for those seeking employment.

Type
Research Article
Copyright
2003 Cambridge University Press

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