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

被引:234
作者
Bentzen, Amalie Kai [1 ]
Marquard, Andrea Marion [2 ]
Lyngaa, Rikke [1 ]
Saini, Sunil Kumar [1 ]
Ramskov, Sofie [1 ]
Donia, Marco [3 ,4 ]
Such, Lina [1 ]
Furness, Andrew J. S. [5 ,6 ]
McGranahan, Nicholas [5 ,7 ]
Rosenthal, Rachel [5 ,7 ]
Straten, Per Thor [3 ,8 ]
Szallasi, Zoltan [2 ]
Svane, Inge Marie [3 ,4 ]
Swanton, Charles [5 ,7 ]
Quezada, Sergio A. [5 ,6 ]
Jakobsen, Soren Nyboe [1 ,9 ]
Eklund, Aron Charles [2 ]
Hadrup, Sine Reker [1 ]
机构
[1] Tech Univ Denmark, Natl Vet Inst, Sect Immunol & Vaccinol, Copenhagen, Denmark
[2] Tech Univ Denmark, Dept Syst Biol, Ctr Biol Sequence Anal, Lyngby, Denmark
[3] Univ Copenhagen, Herlev Hosp, Dept Hematol, Ctr Canc Immune Therapy, Copenhagen, Denmark
[4] Univ Copenhagen, Herlev Hosp, Dept Oncol, Copenhagen, Denmark
[5] UCL Canc Inst, CRUK Lung Canc Ctr Excellence, London, England
[6] UCL, UCL Canc Inst, Canc Immunol Unit, London, England
[7] Francis Crick Inst, Translat Canc Therapeut Lab, London, England
[8] Univ Copenhagen, Dept Immunol & Microbiol, Copenhagen, Denmark
[9] Immudex, Copenhagen, Denmark
基金
英国惠康基金; 英国医学研究理事会;
关键词
PARALLEL DETECTION; MASS CYTOMETRY; SELF-ANTIGEN; RESPONSES; MELANOMA; GENERATION; DESIGN; SENSITIVITY; RECOGNIZES; BLOCKADE;
D O I
10.1038/nbt.3662
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.
引用
收藏
页码:1037 / 1045
页数:9
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