Your browser doesn't support javascript.
loading
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.
Afiliação
  • Moreira ML; René Rachou Institute, Oswaldo Cruz Foundation (FIOCRUZ-MINAS), Belo Horizonte, Minas Gerais, Brazil.
  • Borges-Fernandes LO; Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia.
  • Pascoal-Xavier MA; René Rachou Institute, Oswaldo Cruz Foundation (FIOCRUZ-MINAS), Belo Horizonte, Minas Gerais, Brazil.
  • Ribeiro ÁL; René Rachou Institute, Oswaldo Cruz Foundation (FIOCRUZ-MINAS), Belo Horizonte, Minas Gerais, Brazil.
  • Pereira VHS; School of Medicine, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
  • Pediongco T; René Rachou Institute, Oswaldo Cruz Foundation (FIOCRUZ-MINAS), Belo Horizonte, Minas Gerais, Brazil.
  • Araújo MSDS; René Rachou Institute, Oswaldo Cruz Foundation (FIOCRUZ-MINAS), Belo Horizonte, Minas Gerais, Brazil.
  • Teixeira-Carvalho A; Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia.
  • de Carvalho AL; René Rachou Institute, Oswaldo Cruz Foundation (FIOCRUZ-MINAS), Belo Horizonte, Minas Gerais, Brazil.
  • Mourão MVA; René Rachou Institute, Oswaldo Cruz Foundation (FIOCRUZ-MINAS), Belo Horizonte, Minas Gerais, Brazil.
  • Campos FA; João Paulo II Children's Hospital, Fundação Hospitalar do Estado de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
  • Borges M; João Paulo II Children's Hospital, Fundação Hospitalar do Estado de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
  • Carneiro M; João Paulo II Children's Hospital, Fundação Hospitalar do Estado de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
  • Chen Z; João Paulo II Children's Hospital, Fundação Hospitalar do Estado de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
  • Saunders E; Parasitology Department, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
  • McConville M; Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia.
  • Tsuji M; Department of Biochemistry and Molecular Biology, The University of Melbourne, Melbourne, VIC, Australia.
  • McCluskey J; Department of Biochemistry and Molecular Biology, The University of Melbourne, Melbourne, VIC, Australia.
  • Martins-Filho OA; Aaron Diamond AIDS Research Center, Department of Medicine, Columbia University Irving Medical Center, New York, NY, United States.
  • Eckle SBG; Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia.
  • Coelho-Dos-Reis JGA; René Rachou Institute, Oswaldo Cruz Foundation (FIOCRUZ-MINAS), Belo Horizonte, Minas Gerais, Brazil.
  • Peruhype-Magalhães V; Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia.
Front Immunol ; 13: 926446, 2022.
Article em En | MEDLINE | ID: mdl-36189274
ABSTRACT
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.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células T Invariantes Associadas à Mucosa / Leishmaniose Visceral Tipo de estudo: Risk_factors_studies Limite: Child / Humans Idioma: En Revista: Front Immunol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células T Invariantes Associadas à Mucosa / Leishmaniose Visceral Tipo de estudo: Risk_factors_studies Limite: Child / Humans Idioma: En Revista: Front Immunol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Brasil