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Potential Role of CXCL10 in Monitoring Response to Treatment in Leprosy Patients
The treatment of multibacillary cases of leprosy with multidrug therapy (MDT) comprises 12 doses of a combination of rifampicin, dapsone and clofazimine. Previous studies have described the immunological phenotypic pattern in skin lesions in multibacillary patients. Here, we evaluated the effect of...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329534/ https://www.ncbi.nlm.nih.gov/pubmed/34354699 http://dx.doi.org/10.3389/fimmu.2021.662307 |
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author | Ferreira, Helen Mendes, Mayara Abud de Mattos Barbosa, Mayara Garcia de Oliveira, Eliane Barbosa Sales, Anna Maria Moraes, Milton Ozório Sarno, Euzenir Nunes Pinheiro, Roberta Olmo |
author_facet | Ferreira, Helen Mendes, Mayara Abud de Mattos Barbosa, Mayara Garcia de Oliveira, Eliane Barbosa Sales, Anna Maria Moraes, Milton Ozório Sarno, Euzenir Nunes Pinheiro, Roberta Olmo |
author_sort | Ferreira, Helen |
collection | PubMed |
description | The treatment of multibacillary cases of leprosy with multidrug therapy (MDT) comprises 12 doses of a combination of rifampicin, dapsone and clofazimine. Previous studies have described the immunological phenotypic pattern in skin lesions in multibacillary patients. Here, we evaluated the effect of MDT on skin cell phenotype and on the Mycobacterium leprae-specific immune response. An analysis of skin cell phenotype demonstrated a significant decrease in MRS1 (SR-A), CXCL10 (IP-10) and IFNG (IFN-γ) gene and protein expression after MDT release. Patients were randomized according to whether they experienced a reduction in bacillary load after MDT. A reduction in CXCL10 (IP-10) in sera was associated with the absence of a reduction in the bacillary load at release. Although IFN-γ production in response to M. leprae was not affected by MDT, CXCL10 (IP-10) levels in response to M. leprae increased in cells from patients who experienced a reduction in bacillary load after treatment. Together, our results suggest that CXCL10 (IP-10) may be a good marker for monitoring treatment efficacy in multibacillary patients. |
format | Online Article Text |
id | pubmed-8329534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83295342021-08-04 Potential Role of CXCL10 in Monitoring Response to Treatment in Leprosy Patients Ferreira, Helen Mendes, Mayara Abud de Mattos Barbosa, Mayara Garcia de Oliveira, Eliane Barbosa Sales, Anna Maria Moraes, Milton Ozório Sarno, Euzenir Nunes Pinheiro, Roberta Olmo Front Immunol Immunology The treatment of multibacillary cases of leprosy with multidrug therapy (MDT) comprises 12 doses of a combination of rifampicin, dapsone and clofazimine. Previous studies have described the immunological phenotypic pattern in skin lesions in multibacillary patients. Here, we evaluated the effect of MDT on skin cell phenotype and on the Mycobacterium leprae-specific immune response. An analysis of skin cell phenotype demonstrated a significant decrease in MRS1 (SR-A), CXCL10 (IP-10) and IFNG (IFN-γ) gene and protein expression after MDT release. Patients were randomized according to whether they experienced a reduction in bacillary load after MDT. A reduction in CXCL10 (IP-10) in sera was associated with the absence of a reduction in the bacillary load at release. Although IFN-γ production in response to M. leprae was not affected by MDT, CXCL10 (IP-10) levels in response to M. leprae increased in cells from patients who experienced a reduction in bacillary load after treatment. Together, our results suggest that CXCL10 (IP-10) may be a good marker for monitoring treatment efficacy in multibacillary patients. Frontiers Media S.A. 2021-07-20 /pmc/articles/PMC8329534/ /pubmed/34354699 http://dx.doi.org/10.3389/fimmu.2021.662307 Text en Copyright © 2021 Ferreira, Mendes, de Mattos Barbosa, de Oliveira, Sales, Moraes, Sarno and Pinheiro https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Ferreira, Helen Mendes, Mayara Abud de Mattos Barbosa, Mayara Garcia de Oliveira, Eliane Barbosa Sales, Anna Maria Moraes, Milton Ozório Sarno, Euzenir Nunes Pinheiro, Roberta Olmo Potential Role of CXCL10 in Monitoring Response to Treatment in Leprosy Patients |
title | Potential Role of CXCL10 in Monitoring Response to Treatment in Leprosy Patients |
title_full | Potential Role of CXCL10 in Monitoring Response to Treatment in Leprosy Patients |
title_fullStr | Potential Role of CXCL10 in Monitoring Response to Treatment in Leprosy Patients |
title_full_unstemmed | Potential Role of CXCL10 in Monitoring Response to Treatment in Leprosy Patients |
title_short | Potential Role of CXCL10 in Monitoring Response to Treatment in Leprosy Patients |
title_sort | potential role of cxcl10 in monitoring response to treatment in leprosy patients |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329534/ https://www.ncbi.nlm.nih.gov/pubmed/34354699 http://dx.doi.org/10.3389/fimmu.2021.662307 |
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