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MAIT cell-MR1 reactivity is highly conserved across multiple divergent species.
Edmans, Matthew D; Connelley, Timothy K; Morgan, Sophie; Pediongco, Troi J; Jayaraman, Siddharth; Juno, Jennifer A; Meehan, Bronwyn S; Dewar, Phoebe M; Maze, Emmanuel A; Roos, Eduard O; Paudyal, Basudev; Mak, Jeffrey Y W; Liu, Ligong; Fairlie, David P; Wang, Huimeng; Corbett, Alexandra J; McCluskey, James; Benedictus, Lindert; Tchilian, Elma; Klenerman, Paul; Eckle, Sidonia B G.
Affiliation
  • Edmans MD; Department of Enhanced Host Responses, The Pirbright Institute, Pirbright, United Kingdom; Peter Medawar Building for Pathogen Research, University of Oxford, Oxford, United Kingdom. Electronic address: matthew.edmans@ndm.ox.ac.uk.
  • Connelley TK; Division of Infection and Immunity, The Roslin Institute, The University of Edinburgh, Roslin, United Kingdom.
  • Morgan S; Department of Enhanced Host Responses, The Pirbright Institute, Pirbright, United Kingdom.
  • Pediongco TJ; Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Melbourne, Victoria, Australia.
  • Jayaraman S; Division of Infection and Immunity, The Roslin Institute, The University of Edinburgh, Roslin, United Kingdom.
  • Juno JA; Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Melbourne, Victoria, Australia.
  • Meehan BS; Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Melbourne, Victoria, Australia.
  • Dewar PM; Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Melbourne, Victoria, Australia.
  • Maze EA; Department of Enhanced Host Responses, The Pirbright Institute, Pirbright, United Kingdom.
  • Roos EO; Department of Enhanced Host Responses, The Pirbright Institute, Pirbright, United Kingdom.
  • Paudyal B; Department of Enhanced Host Responses, The Pirbright Institute, Pirbright, United Kingdom.
  • Mak JYW; Centre for Chemistry and Drug Discovery, Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland, Australia; Australian Research Council Centre of Excellence for Innovations in Peptide and Protein Science, Institute for Molecular Bioscience, The University of Queenslan
  • Liu L; Centre for Chemistry and Drug Discovery, Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland, Australia.
  • Fairlie DP; Centre for Chemistry and Drug Discovery, Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland, Australia; Australian Research Council Centre of Excellence for Innovations in Peptide and Protein Science, Institute for Molecular Bioscience, The University of Queenslan
  • Wang H; Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Melbourne, Victoria, Australia; State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Disease, Guangzhou Medical University, Guangzhou, China.
  • Corbett AJ; Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Melbourne, Victoria, Australia.
  • McCluskey J; Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Melbourne, Victoria, Australia.
  • Benedictus L; Division of Infection and Immunity, The Roslin Institute, The University of Edinburgh, Roslin, United Kingdom; Faculty of Veterinary Medicine, Department of Population Health Sciences, Utrecht University, Utrecht, The Netherlands.
  • Tchilian E; Department of Enhanced Host Responses, The Pirbright Institute, Pirbright, United Kingdom.
  • Klenerman P; Peter Medawar Building for Pathogen Research, University of Oxford, Oxford, United Kingdom.
  • Eckle SBG; Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Melbourne, Victoria, Australia. Electronic address: seckle@unimelb.edu.au.
J Biol Chem ; 300(6): 107338, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38705391
ABSTRACT
Mucosal-associated invariant T (MAIT) cells are a subset of unconventional T cells that recognize small molecule metabolites presented by major histocompatibility complex class I related protein 1 (MR1), via an αß T cell receptor (TCR). MAIT TCRs feature an essentially invariant TCR α-chain, which is highly conserved between mammals. Similarly, MR1 is the most highly conserved major histocompatibility complex-I-like molecule. This extreme conservation, including the mode of interaction between the MAIT TCR and MR1, has been shown to allow for species-mismatched reactivities unique in T cell biology, thereby allowing the use of selected species-mismatched MR1-antigen (MR1-Ag) tetramers in comparative immunology studies. However, the pattern of cross-reactivity of species-mismatched MR1-Ag tetramers in identifying MAIT cells in diverse species has not been formally assessed. We developed novel cattle and pig MR1-Ag tetramers and utilized these alongside previously developed human, mouse, and pig-tailed macaque MR1-Ag tetramers to characterize cross-species tetramer reactivities. MR1-Ag tetramers from each species identified T cell populations in distantly related species with specificity that was comparable to species-matched MR1-Ag tetramers. However, there were subtle differences in staining characteristics with practical implications for the accurate identification of MAIT cells. Pig MR1 is sufficiently conserved across species that pig MR1-Ag tetramers identified MAIT cells from the other species. However, MAIT cells in pigs were at the limits of phenotypic detection. In the absence of sheep MR1-Ag tetramers, a MAIT cell population in sheep blood was identified phenotypically, utilizing species-mismatched MR1-Ag tetramers. Collectively, our results validate the use and define the limitations of species-mismatched MR1-Ag tetramers in comparative immunology studies.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Species Specificity / Histocompatibility Antigens Class I / Minor Histocompatibility Antigens / Mucosal-Associated Invariant T Cells Limits: Animals / Humans Language: En Journal: J Biol Chem Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Species Specificity / Histocompatibility Antigens Class I / Minor Histocompatibility Antigens / Mucosal-Associated Invariant T Cells Limits: Animals / Humans Language: En Journal: J Biol Chem Year: 2024 Document type: Article
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