MR1 recycling and blockade of endosomal trafficking reveal distinguishable antigen presentation pathways between Mycobacterium tuberculosis infection and exogenously delivered antigens

[1]  E. Adams,et al.  MR1 displays the microbial metabolome driving selective MR1-restricted T cell receptor usage , 2018, Science Immunology.

[2]  J. McCluskey,et al.  Mucosal‐associated invariant T cell receptor recognition of small molecules presented by MR1 , 2018, Immunology and cell biology.

[3]  E. Karamooz,et al.  MAIT cells and microbial immunity , 2018, Immunology and cell biology.

[4]  M. Flodström-Tullberg,et al.  Severely Impaired Control of Bacterial Infections in a Patient With Cystic Fibrosis Defective in Mucosal-Associated Invariant T Cells. , 2018, Chest.

[5]  J. Villadangos,et al.  How MR1 Presents a Pathogen Metabolic Signature to Mucosal-Associated Invariant T (MAIT) Cells. , 2017, Trends in immunology.

[6]  M. McCormick,et al.  Syntaxin 4 mediates endosome recycling for lytic granule exocytosis in cytotoxic T‐lymphocytes , 2017, Traffic.

[7]  V. Narang,et al.  Functionally diverse human T cells recognize non-microbial antigens presented by MR1 , 2017, eLife.

[8]  D. Speiser,et al.  Heterogeneity assessment of functional T cell avidity , 2017, Scientific Reports.

[9]  J. McCluskey,et al.  Drugs and drug-like molecules can modulate the function of mucosal-associated invariant T cells , 2017, Nature Immunology.

[10]  T. Hawn,et al.  A Polymorphism in Human MR1 is Associated with mRNA Expression and Susceptibility to Tuberculosis , 2016, Genes and Immunity.

[11]  A. Sewell,et al.  Human TRAV1-2-negative MR1-restricted T cells detect S. pyogenes and alternatives to MAIT riboflavin-based antigens , 2016, Nature Communications.

[12]  J. Blander The comings and goings of MHC class I molecules herald a new dawn in cross‐presentation , 2016, Immunological reviews.

[13]  A. Sewell,et al.  Engineering of Isogenic Cells Deficient for MR1 with a CRISPR/Cas9 Lentiviral System: Tools To Study Microbial Antigen Processing and Presentation to Human MR1-Restricted T Cells , 2016, The Journal of Immunology.

[14]  J. McCluskey,et al.  The intracellular pathway for the presentation of vitamin B–related antigens by the antigen-presenting molecule MR1 , 2016, Nature Immunology.

[15]  P. Klenerman,et al.  TLR signaling in human antigen‐presenting cells regulates MR1‐dependent activation of MAIT cells , 2016, European journal of immunology.

[16]  E. Karamooz,et al.  Endosomal MR1 Trafficking Plays a Key Role in Presentation of Mycobacterium tuberculosis Ligands to MAIT Cells , 2016, PLoS pathogens.

[17]  R. Tampé,et al.  TLR Signals Induce Phagosomal MHC-I Delivery from the Endosomal Recycling Compartment to Allow Cross-Presentation , 2014, Cell.

[18]  James McCluskey,et al.  A molecular basis underpinning the T cell receptor heterogeneity of mucosal-associated invariant T cells , 2014, The Journal of experimental medicine.

[19]  O. Lund,et al.  MR1-restricted MAIT cells display ligand discrimination and pathogen selectivity through distinct T cell receptor usage , 2014, The Journal of experimental medicine.

[20]  D. Lewinsohn,et al.  Human Lung Epithelial Cells Contain Mycobacterium tuberculosis in a Late Endosomal Vacuole and Are Efficiently Recognized by CD8+ T Cells , 2014, PloS one.

[21]  D. Sinderen,et al.  T-cell activation by transitory neo-antigens derived from distinct microbial pathways , 2014, Nature.

[22]  James McCluskey,et al.  Recognition of vitamin B metabolites by mucosal-associated invariant T cells , 2013, Nature Communications.

[23]  Peter Cresswell,et al.  Pathways of antigen processing. , 2013, Annual review of immunology.

[24]  Malcolm J. McConville,et al.  MR1 presents microbial vitamin B metabolites to MAIT cells , 2012, Nature.

[25]  K. Tóth,et al.  VAMP4 directs synaptic vesicles to a pool that selectively maintains asynchronous neurotransmission , 2012, Nature Neuroscience.

[26]  Matthew S. Cook,et al.  Human Mucosal Associated Invariant T Cells Detect Bacterially Infected Cells , 2010, PLoS biology.

[27]  M. Kasuga,et al.  The t-SNAREs syntaxin4 and SNAP23 but not v-SNARE VAMP2 are indispensable to tether GLUT4 vesicles at the plasma membrane in adipocyte. , 2010, Biochemical and biophysical research communications.

[28]  D. Lewinsohn,et al.  The Mycobacterium tuberculosis Phagosome Is a HLA-I Processing Competent Organelle , 2009, PLoS pathogens.

[29]  D. Fremont,et al.  MR1 uses an endocytic pathway to activate mucosal-associated invariant T cells , 2008, The Journal of experimental medicine.

[30]  J. Pessin,et al.  Mapping of R-SNARE function at distinct intracellular GLUT4 trafficking steps in adipocytes , 2008, The Journal of cell biology.

[31]  Matthew S. Cook,et al.  Immunodominant Tuberculosis CD8 Antigens Preferentially Restricted by HLA-B , 2007, PLoS pathogens.

[32]  K. Rock,et al.  Important role of cathepsin S in generating peptides for TAP-independent MHC class I crosspresentation in vivo. , 2004, Immunity.