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TRAV1-2+ CD8+ T-cells including oligoconal expansions of MAIT cells are enriched in the airways in human tuberculosis.
Wong, Emily B; Gold, Marielle C; Meermeier, Erin W; Xulu, Bongiwe Z; Khuzwayo, Sharon; Sullivan, Zuri A; Mahyari, Eisa; Rogers, Zoe; Kløverpris, Hénrik; Sharma, Prabhat K; Worley, Aneta H; Lalloo, Umesh; Baijnath, Prinita; Ambaram, Anish; Naidoo, Leon; Suleman, Moosa; Madansein, Rajhmun; McLaren, James E; Ladell, Kristin; Miners, Kelly L; Price, David A; Behar, Samuel M; Nielsen, Morten; Kasprowicz, Victoria O; Leslie, Alasdair; Bishai, William R; Ndung'u, Thumbi; Lewinsohn, David M.
Afiliação
  • Wong EB; 1Africa Health Research Institute, KwaZulu-Natal, South Africa.
  • Gold MC; 2Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA USA.
  • Meermeier EW; 3Harvard Medical School, Boston, MA USA.
  • Xulu BZ; 4Division of Infection and Immunity, University College London, London, UK.
  • Khuzwayo S; 5Department of Pulmonary & Critical Care Medicine, Oregon Health & Science University, Portland, OR USA.
  • Sullivan ZA; 6VA Portland Health Care System, Portland, OR USA.
  • Mahyari E; 7Department of Molecular Microbiology & Immunology, Oregon Health & Science University, Portland, OR USA.
  • Rogers Z; 5Department of Pulmonary & Critical Care Medicine, Oregon Health & Science University, Portland, OR USA.
  • Kløverpris H; 1Africa Health Research Institute, KwaZulu-Natal, South Africa.
  • Sharma PK; 1Africa Health Research Institute, KwaZulu-Natal, South Africa.
  • Worley AH; 1Africa Health Research Institute, KwaZulu-Natal, South Africa.
  • Lalloo U; 8Division of Bioinformatics and Computational Biology (BCB), Department of Medical Informatics and Clinical Epidemiology (DMICE), Oregon Health & Science University, Portland, OR USA.
  • Baijnath P; 1Africa Health Research Institute, KwaZulu-Natal, South Africa.
  • Ambaram A; 1Africa Health Research Institute, KwaZulu-Natal, South Africa.
  • Naidoo L; 4Division of Infection and Immunity, University College London, London, UK.
  • Suleman M; 9Institute for Immunology and Microbiology, University of Copenhagen, Copenhagen, Denmark.
  • Madansein R; 6VA Portland Health Care System, Portland, OR USA.
  • McLaren JE; 6VA Portland Health Care System, Portland, OR USA.
  • Ladell K; 10Durban University of Technology, Durban, South Africa.
  • Miners KL; 10Durban University of Technology, Durban, South Africa.
  • Price DA; Department of Pulmonology, Inkosi Albert Luthuli Hospital, Durban, South Africa.
  • Behar SM; Department of Pulmonology, Inkosi Albert Luthuli Hospital, Durban, South Africa.
  • Nielsen M; Department of Pulmonology, Inkosi Albert Luthuli Hospital, Durban, South Africa.
  • Kasprowicz VO; Department of Pulmonology, Inkosi Albert Luthuli Hospital, Durban, South Africa.
  • Leslie A; 12Department of Pulmonology & Critical Care, Nelson R. Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa.
  • Bishai WR; 13Department of Cardiothoracic Surgery, Nelson R. Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa.
  • Ndung'u T; 14Centre for AIDS Programme of Research in South Africa (CAPRISA), Durban, South Africa.
  • Lewinsohn DM; 15Institute of Infection & Immunity, Cardiff University School of Medicine, Cardiff, Wales UK.
Commun Biol ; 2: 203, 2019.
Article em En | MEDLINE | ID: mdl-31231693
Mucosal-associated invariant T (MAIT) cells typically express a TRAV1-2+ semi-invariant TCRα that enables recognition of bacterial, mycobacterial, and fungal riboflavin metabolites presented by MR1. MAIT cells are associated with immune control of bacterial and mycobacterial infections in murine models. Here, we report that a population of pro-inflammatory TRAV1-2+ CD8+ T cells are present in the airways and lungs of healthy individuals and are enriched in bronchoalveolar fluid of patients with active pulmonary tuberculosis (TB). High-throughput T cell receptor analysis reveals oligoclonal expansions of canonical and donor-unique TRAV1-2+ MAIT-consistent TCRα sequences within this population. Some of these cells demonstrate MR1-restricted mycobacterial reactivity and phenotypes suggestive of MAIT cell identity. These findings demonstrate enrichment of TRAV1-2+ CD8+ T cells with MAIT or MAIT-like features in the airways during active TB and suggest a role for these cells in the human pulmonary immune response to Mycobacterium tuberculosis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tuberculose Pulmonar / Linfócitos T CD8-Positivos / Células T Invariantes Associadas à Mucosa Tipo de estudo: Prognostic_studies Limite: Animals / Humans País/Região como assunto: Africa / America do norte Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tuberculose Pulmonar / Linfócitos T CD8-Positivos / Células T Invariantes Associadas à Mucosa Tipo de estudo: Prognostic_studies Limite: Animals / Humans País/Região como assunto: Africa / America do norte Idioma: En Ano de publicação: 2019 Tipo de documento: Article