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Ceruloplasmin, transferrin and apolipoprotein A-II play important role in treatment's follow-up of paracoccidioidomycosis patients

Paracoccidioidomycosis (PCM) is a systemic disease caused by thermodymorphic fungi of the Paracoccidioides brasiliensis complex, (Paracoccidioides spp.). Patients with PCM reveal specific cellular immune impairment. Despite the effective treatment, quiescent fungi can lead to relapse, usually late,...

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Autores principales: Sylvestre, Tatiane Fernanda, Cavalcante, Ricardo de Souza, da Silva, Julhiany de Fátima, Paniago, Anamaria Mello Miranda, Weber, Simone Schneider, Pauletti, Bianca Alves, de Carvalho, Lídia Raquel, dos Santos, Lucilene Delazari, Mendes, Rinaldo Poncio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6201901/
https://www.ncbi.nlm.nih.gov/pubmed/30359420
http://dx.doi.org/10.1371/journal.pone.0206051
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author Sylvestre, Tatiane Fernanda
Cavalcante, Ricardo de Souza
da Silva, Julhiany de Fátima
Paniago, Anamaria Mello Miranda
Weber, Simone Schneider
Pauletti, Bianca Alves
de Carvalho, Lídia Raquel
dos Santos, Lucilene Delazari
Mendes, Rinaldo Poncio
author_facet Sylvestre, Tatiane Fernanda
Cavalcante, Ricardo de Souza
da Silva, Julhiany de Fátima
Paniago, Anamaria Mello Miranda
Weber, Simone Schneider
Pauletti, Bianca Alves
de Carvalho, Lídia Raquel
dos Santos, Lucilene Delazari
Mendes, Rinaldo Poncio
author_sort Sylvestre, Tatiane Fernanda
collection PubMed
description Paracoccidioidomycosis (PCM) is a systemic disease caused by thermodymorphic fungi of the Paracoccidioides brasiliensis complex, (Paracoccidioides spp.). Patients with PCM reveal specific cellular immune impairment. Despite the effective treatment, quiescent fungi can lead to relapse, usually late, the serological diagnosis of which has been deficient. The present study was carried out with the objective of investigating a biomarker for the identification of PCM relapse and another molecule behaving as an immunological recovery biomarker; therefore, it may be used as a cure criterion. In the evolutionary analysis of the proteins identified in PCM patients, comparing those that presented with those that did not reveal relapse, 29 proteins were identified. The interactions observed between the proteins, using transferrin and haptoglobin, as the main binding protein, were strong with all the others. Patient follow-up suggests that cerulosplamin may be a marker of relapse and that transferrin and apolipoprotein A-II may contribute to the evaluation of the treatment efficacy and avoiding a premature decision.
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spelling pubmed-62019012018-11-19 Ceruloplasmin, transferrin and apolipoprotein A-II play important role in treatment's follow-up of paracoccidioidomycosis patients Sylvestre, Tatiane Fernanda Cavalcante, Ricardo de Souza da Silva, Julhiany de Fátima Paniago, Anamaria Mello Miranda Weber, Simone Schneider Pauletti, Bianca Alves de Carvalho, Lídia Raquel dos Santos, Lucilene Delazari Mendes, Rinaldo Poncio PLoS One Research Article Paracoccidioidomycosis (PCM) is a systemic disease caused by thermodymorphic fungi of the Paracoccidioides brasiliensis complex, (Paracoccidioides spp.). Patients with PCM reveal specific cellular immune impairment. Despite the effective treatment, quiescent fungi can lead to relapse, usually late, the serological diagnosis of which has been deficient. The present study was carried out with the objective of investigating a biomarker for the identification of PCM relapse and another molecule behaving as an immunological recovery biomarker; therefore, it may be used as a cure criterion. In the evolutionary analysis of the proteins identified in PCM patients, comparing those that presented with those that did not reveal relapse, 29 proteins were identified. The interactions observed between the proteins, using transferrin and haptoglobin, as the main binding protein, were strong with all the others. Patient follow-up suggests that cerulosplamin may be a marker of relapse and that transferrin and apolipoprotein A-II may contribute to the evaluation of the treatment efficacy and avoiding a premature decision. Public Library of Science 2018-10-25 /pmc/articles/PMC6201901/ /pubmed/30359420 http://dx.doi.org/10.1371/journal.pone.0206051 Text en © 2018 Sylvestre 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
Sylvestre, Tatiane Fernanda
Cavalcante, Ricardo de Souza
da Silva, Julhiany de Fátima
Paniago, Anamaria Mello Miranda
Weber, Simone Schneider
Pauletti, Bianca Alves
de Carvalho, Lídia Raquel
dos Santos, Lucilene Delazari
Mendes, Rinaldo Poncio
Ceruloplasmin, transferrin and apolipoprotein A-II play important role in treatment's follow-up of paracoccidioidomycosis patients
title Ceruloplasmin, transferrin and apolipoprotein A-II play important role in treatment's follow-up of paracoccidioidomycosis patients
title_full Ceruloplasmin, transferrin and apolipoprotein A-II play important role in treatment's follow-up of paracoccidioidomycosis patients
title_fullStr Ceruloplasmin, transferrin and apolipoprotein A-II play important role in treatment's follow-up of paracoccidioidomycosis patients
title_full_unstemmed Ceruloplasmin, transferrin and apolipoprotein A-II play important role in treatment's follow-up of paracoccidioidomycosis patients
title_short Ceruloplasmin, transferrin and apolipoprotein A-II play important role in treatment's follow-up of paracoccidioidomycosis patients
title_sort ceruloplasmin, transferrin and apolipoprotein a-ii play important role in treatment's follow-up of paracoccidioidomycosis patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6201901/
https://www.ncbi.nlm.nih.gov/pubmed/30359420
http://dx.doi.org/10.1371/journal.pone.0206051
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