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Infection of dogs by Leishmania infantum elicits a general response of IgG subclasses
Leishmania infantum is the etiological agent of zoonotic visceral leishmaniasis. In endemic areas, canine infections are considered the main source of infection for human populations. Therefore, any control of human leishmaniasis must include the control of canine infections. Chemotherapy of leishma...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7606601/ https://www.ncbi.nlm.nih.gov/pubmed/33139752 http://dx.doi.org/10.1038/s41598-020-75569-6 |
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author | Olías-Molero, A. I. Moreno, I. Corral, M. J. Jiménez-Antón, M. D. Day, M. J. Domínguez, M. Alunda, J. M. |
author_facet | Olías-Molero, A. I. Moreno, I. Corral, M. J. Jiménez-Antón, M. D. Day, M. J. Domínguez, M. Alunda, J. M. |
author_sort | Olías-Molero, A. I. |
collection | PubMed |
description | Leishmania infantum is the etiological agent of zoonotic visceral leishmaniasis. In endemic areas, canine infections are considered the main source of infection for human populations. Therefore, any control of human leishmaniasis must include the control of canine infections. Chemotherapy of leishmaniasis is inadequate and canine immunoprophylaxis has important limitations. Reports on the response of infected dogs are abundant but no clear picture of immune events has emerged. To shed some light on these shortcomings the specific IgG subclass response was followed in 20 Beagle dogs experimentally infected with L. infantum using monoclonal antibodies (MAb) specific for canine IgG(1), IgG(2), IgG(3) and IgG(4), along with ELISA and flow cytometry. Results showed that parasitic infection elicits a general response of all IgG subclasses, with a predominant IgG(1) response and without any evidence of IgG(1)/IgG(2) dichotomy. These findings suggest that the inconsistent results reported previously could be related to the lack of specific reagents and not to the actual differences in the immune response of infected animals. Differential IgG subclass reactivity in ELISA and cytometry and the analysis of the reacting antigens could facilitate the diagnosis and prognosis of the disease and provide a useful tool for adequate therapeutics and vaccine development against leishmaniasis. |
format | Online Article Text |
id | pubmed-7606601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76066012020-11-05 Infection of dogs by Leishmania infantum elicits a general response of IgG subclasses Olías-Molero, A. I. Moreno, I. Corral, M. J. Jiménez-Antón, M. D. Day, M. J. Domínguez, M. Alunda, J. M. Sci Rep Article Leishmania infantum is the etiological agent of zoonotic visceral leishmaniasis. In endemic areas, canine infections are considered the main source of infection for human populations. Therefore, any control of human leishmaniasis must include the control of canine infections. Chemotherapy of leishmaniasis is inadequate and canine immunoprophylaxis has important limitations. Reports on the response of infected dogs are abundant but no clear picture of immune events has emerged. To shed some light on these shortcomings the specific IgG subclass response was followed in 20 Beagle dogs experimentally infected with L. infantum using monoclonal antibodies (MAb) specific for canine IgG(1), IgG(2), IgG(3) and IgG(4), along with ELISA and flow cytometry. Results showed that parasitic infection elicits a general response of all IgG subclasses, with a predominant IgG(1) response and without any evidence of IgG(1)/IgG(2) dichotomy. These findings suggest that the inconsistent results reported previously could be related to the lack of specific reagents and not to the actual differences in the immune response of infected animals. Differential IgG subclass reactivity in ELISA and cytometry and the analysis of the reacting antigens could facilitate the diagnosis and prognosis of the disease and provide a useful tool for adequate therapeutics and vaccine development against leishmaniasis. Nature Publishing Group UK 2020-11-02 /pmc/articles/PMC7606601/ /pubmed/33139752 http://dx.doi.org/10.1038/s41598-020-75569-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Olías-Molero, A. I. Moreno, I. Corral, M. J. Jiménez-Antón, M. D. Day, M. J. Domínguez, M. Alunda, J. M. Infection of dogs by Leishmania infantum elicits a general response of IgG subclasses |
title | Infection of dogs by Leishmania infantum elicits a general response of IgG subclasses |
title_full | Infection of dogs by Leishmania infantum elicits a general response of IgG subclasses |
title_fullStr | Infection of dogs by Leishmania infantum elicits a general response of IgG subclasses |
title_full_unstemmed | Infection of dogs by Leishmania infantum elicits a general response of IgG subclasses |
title_short | Infection of dogs by Leishmania infantum elicits a general response of IgG subclasses |
title_sort | infection of dogs by leishmania infantum elicits a general response of igg subclasses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7606601/ https://www.ncbi.nlm.nih.gov/pubmed/33139752 http://dx.doi.org/10.1038/s41598-020-75569-6 |
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