Literature DB >> 27571370

Large-scale detection of antigen-specific T cells using peptide-MHC-I multimers labeled with DNA barcodes.

Amalie Kai Bentzen1, Andrea Marion Marquard2, Rikke Lyngaa1, Sunil Kumar Saini1, Sofie Ramskov1, Marco Donia3,4, Lina Such1, Andrew J S Furness5,6, Nicholas McGranahan5,7, Rachel Rosenthal5,7, Per Thor Straten3,8, Zoltan Szallasi2, Inge Marie Svane3,4, Charles Swanton5,7, Sergio A Quezada5,6, Søren Nyboe Jakobsen1,9, Aron Charles Eklund2, Sine Reker Hadrup1.   

Abstract

Identification of the peptides recognized by individual T cells is important for understanding and treating immune-related diseases. Current cytometry-based approaches are limited to the simultaneous screening of 10-100 distinct T-cell specificities in one sample. Here we use peptide-major histocompatibility complex (MHC) multimers labeled with individual DNA barcodes to screen >1,000 peptide specificities in a single sample, and detect low-frequency CD8 T cells specific for virus- or cancer-restricted antigens. When analyzing T-cell recognition of shared melanoma antigens before and after adoptive cell therapy in melanoma patients, we observe a greater number of melanoma-specific T-cell populations compared with cytometry-based approaches. Furthermore, we detect neoepitope-specific T cells in tumor-infiltrating lymphocytes and peripheral blood from patients with non-small cell lung cancer. Barcode-labeled pMHC multimers enable the combination of functional T-cell analysis with large-scale epitope recognition profiling for the characterization of T-cell recognition in various diseases, including in small clinical samples.

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Year:  2016        PMID: 27571370     DOI: 10.1038/nbt.3662

Source DB:  PubMed          Journal:  Nat Biotechnol        ISSN: 1087-0156            Impact factor:   54.908


  50 in total

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2.  Generation of peptide-MHC class I complexes through UV-mediated ligand exchange.

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3.  Conditional MHC class I ligands and peptide exchange technology for the human MHC gene products HLA-A1, -A3, -A11, and -B7.

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5.  HLA-A2-peptide complexes: refolding and crystallization of molecules expressed in Escherichia coli and complexed with single antigenic peptides.

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6.  T-cell responses to oncogenic merkel cell polyomavirus proteins distinguish patients with merkel cell carcinoma from healthy donors.

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2.  Improved peptide-MHC class II interaction prediction through integration of eluted ligand and peptide affinity data.

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10.  Optimized combinatorial pMHC class II multimer labeling for precision immune monitoring of tumor-specific CD4 T cells in patients.

Authors:  Georg Alexander Rockinger; Philippe Guillaume; Amélie Cachot; Margaux Saillard; Daniel E Speiser; Georges Coukos; Alexandre Harari; Pedro J Romero; Julien Schmidt; Camilla Jandus
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