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The role of mucosal-associated invariant T cells in visceral leishmaniasis
Mucosal-associated invariant T (MAIT) cells are restricted by MR1 and are known to protect against bacterial and viral infections. Our understanding of the role of MAIT cells in parasitic infections, such as visceral leishmaniasis (VL) caused by protozoan parasites of Leishmania donovani, is limited...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9521739/ https://www.ncbi.nlm.nih.gov/pubmed/36189274 http://dx.doi.org/10.3389/fimmu.2022.926446 |
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author | Moreira, Marcela de Lima Borges-Fernandes, Luana Oliveira Pascoal-Xavier, Marcelo Antônio Ribeiro, Ágata Lopes Pereira, Victória Hellena Silva Pediongco, Troi Araújo, Márcio Sobreira da Silva Teixeira-Carvalho, Andréa de Carvalho, Andrea Lucchesi Mourão, Maria Vitória Assumpção Campos, Flávia Alves Borges, Marineide Carneiro, Mariângela Chen, Zhenjun Saunders, Eleanor McConville, Malcolm Tsuji, Moriya McCluskey, James Martins-Filho, Olindo Assis Eckle, Sidonia Barbara Guiomar Coelho-dos-Reis, Jordana Grazziela Alves Peruhype-Magalhães, Vanessa |
author_facet | Moreira, Marcela de Lima Borges-Fernandes, Luana Oliveira Pascoal-Xavier, Marcelo Antônio Ribeiro, Ágata Lopes Pereira, Victória Hellena Silva Pediongco, Troi Araújo, Márcio Sobreira da Silva Teixeira-Carvalho, Andréa de Carvalho, Andrea Lucchesi Mourão, Maria Vitória Assumpção Campos, Flávia Alves Borges, Marineide Carneiro, Mariângela Chen, Zhenjun Saunders, Eleanor McConville, Malcolm Tsuji, Moriya McCluskey, James Martins-Filho, Olindo Assis Eckle, Sidonia Barbara Guiomar Coelho-dos-Reis, Jordana Grazziela Alves Peruhype-Magalhães, Vanessa |
author_sort | Moreira, Marcela de Lima |
collection | PubMed |
description | Mucosal-associated invariant T (MAIT) cells are restricted by MR1 and are known to protect against bacterial and viral infections. Our understanding of the role of MAIT cells in parasitic infections, such as visceral leishmaniasis (VL) caused by protozoan parasites of Leishmania donovani, is limited. This study showed that in response to L. infantum, human peripheral blood MAIT cells from children with leishmaniasis produced TNF and IFN-γ in an MR1-dependent manner. The overall frequency of MAIT cells was inversely correlated with alanine aminotransferase levels, a specific marker of liver damage strongly associated with severe hepatic involvement in VL. In addition, there was a positive correlation between total protein levels and the frequency of IL-17A(+) CD8(+) MAIT cells, whereby reduced total protein levels are a marker of liver and kidney damage. Furthermore, the frequencies of IFN-γ(+) and IL-10(+) MAIT cells were inversely correlated with hemoglobin levels, a marker of severe anemia. In asymptomatic individuals and VL patients after treatment, MAIT cells also produced IL-17A, a cytokine signature associated with resistance to visceral leishmaniasis, suggesting that MAIT cells play important role in protecting against VL. In summary, these results broaden our understanding of MAIT-cell immunity to include protection against parasitic infections, with implications for MAIT-cell-based therapeutics and vaccines. At last, this study paves the way for the investigation of putative MAIT cell antigens that could exist in the context of Leishmania infection. |
format | Online Article Text |
id | pubmed-9521739 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95217392022-09-30 The role of mucosal-associated invariant T cells in visceral leishmaniasis Moreira, Marcela de Lima Borges-Fernandes, Luana Oliveira Pascoal-Xavier, Marcelo Antônio Ribeiro, Ágata Lopes Pereira, Victória Hellena Silva Pediongco, Troi Araújo, Márcio Sobreira da Silva Teixeira-Carvalho, Andréa de Carvalho, Andrea Lucchesi Mourão, Maria Vitória Assumpção Campos, Flávia Alves Borges, Marineide Carneiro, Mariângela Chen, Zhenjun Saunders, Eleanor McConville, Malcolm Tsuji, Moriya McCluskey, James Martins-Filho, Olindo Assis Eckle, Sidonia Barbara Guiomar Coelho-dos-Reis, Jordana Grazziela Alves Peruhype-Magalhães, Vanessa Front Immunol Immunology Mucosal-associated invariant T (MAIT) cells are restricted by MR1 and are known to protect against bacterial and viral infections. Our understanding of the role of MAIT cells in parasitic infections, such as visceral leishmaniasis (VL) caused by protozoan parasites of Leishmania donovani, is limited. This study showed that in response to L. infantum, human peripheral blood MAIT cells from children with leishmaniasis produced TNF and IFN-γ in an MR1-dependent manner. The overall frequency of MAIT cells was inversely correlated with alanine aminotransferase levels, a specific marker of liver damage strongly associated with severe hepatic involvement in VL. In addition, there was a positive correlation between total protein levels and the frequency of IL-17A(+) CD8(+) MAIT cells, whereby reduced total protein levels are a marker of liver and kidney damage. Furthermore, the frequencies of IFN-γ(+) and IL-10(+) MAIT cells were inversely correlated with hemoglobin levels, a marker of severe anemia. In asymptomatic individuals and VL patients after treatment, MAIT cells also produced IL-17A, a cytokine signature associated with resistance to visceral leishmaniasis, suggesting that MAIT cells play important role in protecting against VL. In summary, these results broaden our understanding of MAIT-cell immunity to include protection against parasitic infections, with implications for MAIT-cell-based therapeutics and vaccines. At last, this study paves the way for the investigation of putative MAIT cell antigens that could exist in the context of Leishmania infection. Frontiers Media S.A. 2022-09-15 /pmc/articles/PMC9521739/ /pubmed/36189274 http://dx.doi.org/10.3389/fimmu.2022.926446 Text en Copyright © 2022 Moreira, Borges-Fernandes, Pascoal-Xavier, Ribeiro, Pereira, Pediongco, Araújo, Teixeira-Carvalho, de Carvalho, Mourão, Campos, Borges, Carneiro, Chen, Saunders, McConville, Tsuji, McCluskey, Martins-Filho, Eckle, Coelho-dos-Reis and Peruhype-Magalhães 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 Moreira, Marcela de Lima Borges-Fernandes, Luana Oliveira Pascoal-Xavier, Marcelo Antônio Ribeiro, Ágata Lopes Pereira, Victória Hellena Silva Pediongco, Troi Araújo, Márcio Sobreira da Silva Teixeira-Carvalho, Andréa de Carvalho, Andrea Lucchesi Mourão, Maria Vitória Assumpção Campos, Flávia Alves Borges, Marineide Carneiro, Mariângela Chen, Zhenjun Saunders, Eleanor McConville, Malcolm Tsuji, Moriya McCluskey, James Martins-Filho, Olindo Assis Eckle, Sidonia Barbara Guiomar Coelho-dos-Reis, Jordana Grazziela Alves Peruhype-Magalhães, Vanessa The role of mucosal-associated invariant T cells in visceral leishmaniasis |
title | The role of mucosal-associated invariant T cells in visceral leishmaniasis |
title_full | The role of mucosal-associated invariant T cells in visceral leishmaniasis |
title_fullStr | The role of mucosal-associated invariant T cells in visceral leishmaniasis |
title_full_unstemmed | The role of mucosal-associated invariant T cells in visceral leishmaniasis |
title_short | The role of mucosal-associated invariant T cells in visceral leishmaniasis |
title_sort | role of mucosal-associated invariant t cells in visceral leishmaniasis |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9521739/ https://www.ncbi.nlm.nih.gov/pubmed/36189274 http://dx.doi.org/10.3389/fimmu.2022.926446 |
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