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