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Detection of IgG Anti-Leishmania Antigen by Flow Cytometry as a Diagnostic Test for Cutaneous Leishmaniasis

Diagnosis of cutaneous leishmaniasis (CL) relies on clinical presentation, parasite isolation, histopathologic evaluation and positive Montenegro skin test. However, the low amounts of parasites in the lesion of these individuals make parasite isolation and histopatologic diagnosis unreliable, often...

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Autores principales: Pedral-Sampaio, Geraldo, Alves, Jessé S., Schriefer, Albert, Magalhães, Andréa, Meyer, Roberto, Glesby, Marshall J., Carvalho, Edgar M., Carvalho, Lucas P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5021300/
https://www.ncbi.nlm.nih.gov/pubmed/27622535
http://dx.doi.org/10.1371/journal.pone.0162793
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author Pedral-Sampaio, Geraldo
Alves, Jessé S.
Schriefer, Albert
Magalhães, Andréa
Meyer, Roberto
Glesby, Marshall J.
Carvalho, Edgar M.
Carvalho, Lucas P.
author_facet Pedral-Sampaio, Geraldo
Alves, Jessé S.
Schriefer, Albert
Magalhães, Andréa
Meyer, Roberto
Glesby, Marshall J.
Carvalho, Edgar M.
Carvalho, Lucas P.
author_sort Pedral-Sampaio, Geraldo
collection PubMed
description Diagnosis of cutaneous leishmaniasis (CL) relies on clinical presentation, parasite isolation, histopathologic evaluation and positive Montenegro skin test. However, the low amounts of parasites in the lesion of these individuals make parasite isolation and histopatologic diagnosis unreliable, often leading to false-negative results. Also, 15% of people living in endemic areas have sub-clinical infection characterized by positive Montenegro skin test, which may contribute to misdiagnosis. Although the main Leishmania killing mechanism is through cell-mediated immune response, antibodies against Leishmania antigens are found in infected individuals. Here our goal was to develop a new serological technique using polystyrene microspheres sensitized with soluble Leishmania antigens as a tool for the detection of IgG in serum from CL patients by flow cytometry. To validate the assay we carried out a comparative test (ELISA) commonly used as a diagnostic test for parasitic diseases. To determine cross-reactivity we used serum from patients with Chagas disease, caused by a trypanosome that has several proteins with high homology to those of the Leishmania genus. We observed that the flow cytometry technique was more sensitive than the ELISA, but, less specific. Our results show that the flow cytometry serologic test can be used to confirm CL cases in L. braziliensis transmission areas, however, presence of Chagas disease has to be ruled out in these individuals.
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spelling pubmed-50213002016-09-27 Detection of IgG Anti-Leishmania Antigen by Flow Cytometry as a Diagnostic Test for Cutaneous Leishmaniasis Pedral-Sampaio, Geraldo Alves, Jessé S. Schriefer, Albert Magalhães, Andréa Meyer, Roberto Glesby, Marshall J. Carvalho, Edgar M. Carvalho, Lucas P. PLoS One Research Article Diagnosis of cutaneous leishmaniasis (CL) relies on clinical presentation, parasite isolation, histopathologic evaluation and positive Montenegro skin test. However, the low amounts of parasites in the lesion of these individuals make parasite isolation and histopatologic diagnosis unreliable, often leading to false-negative results. Also, 15% of people living in endemic areas have sub-clinical infection characterized by positive Montenegro skin test, which may contribute to misdiagnosis. Although the main Leishmania killing mechanism is through cell-mediated immune response, antibodies against Leishmania antigens are found in infected individuals. Here our goal was to develop a new serological technique using polystyrene microspheres sensitized with soluble Leishmania antigens as a tool for the detection of IgG in serum from CL patients by flow cytometry. To validate the assay we carried out a comparative test (ELISA) commonly used as a diagnostic test for parasitic diseases. To determine cross-reactivity we used serum from patients with Chagas disease, caused by a trypanosome that has several proteins with high homology to those of the Leishmania genus. We observed that the flow cytometry technique was more sensitive than the ELISA, but, less specific. Our results show that the flow cytometry serologic test can be used to confirm CL cases in L. braziliensis transmission areas, however, presence of Chagas disease has to be ruled out in these individuals. Public Library of Science 2016-09-13 /pmc/articles/PMC5021300/ /pubmed/27622535 http://dx.doi.org/10.1371/journal.pone.0162793 Text en © 2016 Pedral-Sampaio et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Pedral-Sampaio, Geraldo
Alves, Jessé S.
Schriefer, Albert
Magalhães, Andréa
Meyer, Roberto
Glesby, Marshall J.
Carvalho, Edgar M.
Carvalho, Lucas P.
Detection of IgG Anti-Leishmania Antigen by Flow Cytometry as a Diagnostic Test for Cutaneous Leishmaniasis
title Detection of IgG Anti-Leishmania Antigen by Flow Cytometry as a Diagnostic Test for Cutaneous Leishmaniasis
title_full Detection of IgG Anti-Leishmania Antigen by Flow Cytometry as a Diagnostic Test for Cutaneous Leishmaniasis
title_fullStr Detection of IgG Anti-Leishmania Antigen by Flow Cytometry as a Diagnostic Test for Cutaneous Leishmaniasis
title_full_unstemmed Detection of IgG Anti-Leishmania Antigen by Flow Cytometry as a Diagnostic Test for Cutaneous Leishmaniasis
title_short Detection of IgG Anti-Leishmania Antigen by Flow Cytometry as a Diagnostic Test for Cutaneous Leishmaniasis
title_sort detection of igg anti-leishmania antigen by flow cytometry as a diagnostic test for cutaneous leishmaniasis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5021300/
https://www.ncbi.nlm.nih.gov/pubmed/27622535
http://dx.doi.org/10.1371/journal.pone.0162793
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