T-Scan: A Genome-wide Method for the Systematic Discovery of T Cell Epitopes

T cell recognition of specific antigens mediates protection from pathogens and controls neoplasias, but can also cause autoimmunity. Our knowledge of T cell antigens and their implications for human health is limited by the technical limitations of T cell profiling technologies. Here, we present T-S...

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Published in:Cell Vol. 178; no. 4; pp. 1016 - 1028.e13
Main Authors: Kula, Tomasz, Dezfulian, Mohammad H., Wang, Charlotte I., Abdelfattah, Nouran S., Hartman, Zachary C., Wucherpfennig, Kai W., Lyerly, Herbert Kim, Elledge, Stephen J.
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Language:English
Published: United States Elsevier Inc 08-08-2019
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Abstract T cell recognition of specific antigens mediates protection from pathogens and controls neoplasias, but can also cause autoimmunity. Our knowledge of T cell antigens and their implications for human health is limited by the technical limitations of T cell profiling technologies. Here, we present T-Scan, a high-throughput platform for identification of antigens productively recognized by T cells. T-Scan uses lentiviral delivery of antigen libraries into cells for endogenous processing and presentation on major histocompatibility complex (MHC) molecules. Target cells functionally recognized by T cells are isolated using a reporter for granzyme B activity, and the antigens mediating recognition are identified by next-generation sequencing. We show T-Scan correctly identifies cognate antigens of T cell receptors (TCRs) from viral and human genome-wide libraries. We apply T-Scan to discover new viral antigens, perform high-resolution mapping of TCR specificity, and characterize the reactivity of a tumor-derived TCR. T-Scan is a powerful approach for studying T cell responses. [Display omitted] •T-Scan is a high-throughput method to identify the functional targets of CD8 T cells•We apply T-Scan to multiplex discovery of CMV antigens from bulk memory T cells•Genome-wide T-Scan finds the cognate antigen and off-targets of a self-reactive TCR T-Scan is a cell-based, pooled screening approach for high-throughput identification of antigens productively recognized by T cells.
AbstractList T cell recognition of specific antigens mediates protection from pathogens and controls neoplasias, but can also cause autoimmunity. Our knowledge of T cell antigens and their implications for human health is limited by the technical limitations of T cell profiling technologies. Here, we present T-Scan, a high-throughput platform for identification of antigens productively recognized by T cells. T-Scan uses lentiviral delivery of antigen libraries into cells for endogenous processing and presentation on major histocompatibility complex (MHC) molecules. Target cells functionally recognized by T cells are isolated using a reporter for granzyme B activity, and the antigens mediating recognition are identified by next-generation sequencing. We show T-Scan correctly identifies cognate antigens of T cell receptors (TCRs) from viral and human genome-wide libraries. We apply T-Scan to discover new viral antigens, perform high-resolution mapping of TCR specificity, and characterize the reactivity of a tumor-derived TCR. T-Scan is a powerful approach for studying T cell responses.
T cell recognition of specific antigens mediates protection from pathogens and controls neoplasias, but can also cause autoimmunity. Our knowledge of T cell antigens and their implications for human health is limited by the technical limitations of T cell profiling technologies. Here, we present T-Scan, a high-throughput platform for identification of antigens productively recognized by T cells. T-Scan uses lentiviral delivery of antigen libraries into cells for endogenous processing and presentation on major histocompatibility complex (MHC) molecules. Target cells functionally recognized by T cells are isolated using a reporter for granzyme B activity, and the antigens mediating recognition are identified by next-generation sequencing. We show T-Scan correctly identifies cognate antigens of T cell receptors (TCRs) from viral and human genome-wide libraries. We apply T-Scan to discover new viral antigens, perform high-resolution mapping of TCR specificity, and characterize the reactivity of a tumor-derived TCR. T-Scan is a powerful approach for studying T cell responses. [Display omitted] •T-Scan is a high-throughput method to identify the functional targets of CD8 T cells•We apply T-Scan to multiplex discovery of CMV antigens from bulk memory T cells•Genome-wide T-Scan finds the cognate antigen and off-targets of a self-reactive TCR T-Scan is a cell-based, pooled screening approach for high-throughput identification of antigens productively recognized by T cells.
T cell recognition of specific antigens mediates protection from pathogens and controls neoplasias, but can also cause autoimmunity. Our knowledge of T cell antigens and their implications for human health is limited by the technical limitations of T cell profiling technologies. Here, we present T-Scan, a high-throughput platform for identification of antigens productively recognized by T cells. T-Scan uses lentiviral delivery of antigen libraries into cells for endogenous processing and presentation on major histocompatibility complex (MHC) molecules. Target cells functionally recognized by T cells are isolated using a reporter for granzyme B activity, and the antigens mediating recognition are identified by next-generation sequencing. We show T-Scan correctly identifies cognate antigens of T cell receptors (TCRs) from viral and human genome-wide libraries. We apply T-Scan to discover new viral antigens, perform high-resolution mapping of TCR specificity, and characterize the reactivity of a tumor-derived TCR. T-Scan is a powerful approach for studying T cell responses. T-Scan is a cell-based, pooled screening approach for high-throughput identification of antigens productively recognized by T cells.
Author Dezfulian, Mohammad H.
Abdelfattah, Nouran S.
Hartman, Zachary C.
Wucherpfennig, Kai W.
Kula, Tomasz
Lyerly, Herbert Kim
Elledge, Stephen J.
Wang, Charlotte I.
AuthorAffiliation 4 Departments of Surgery and Pathology, Duke University Medical Center, 571 Research Drive, Suite 433, Box 2606, Durham, NC 27710, USA
6 Departments of Surgery, Immunology, and Pathology, Duke University Medical Center, 571 Research Drive, Suite 433, Box 2606, Durham, NC 27710, USA
3 Department of Pathology, Massachusetts General Hospital, Boston, MA, USA
7 Lead Contact
1 Division of Genetics, Department of Medicine, Howard Hughes Medical Institute, Brigham and Women’s Hospital, Boston, MA 02115, USA
5 Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Department of Immunobiology, Harvard Medical School, Boston, MA 02115, USA
2 Department of Genetics, Harvard University Medical School, Boston, MA, USA
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ContentType Journal Article
Copyright 2019 Elsevier Inc.
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Issue 4
Keywords TCR-specificity
peptide MHC recognition
epitope discovery
T cell screening
TCR epitope
off-target screening
T cell epitope
immunological screening
antigen discovery
epitope screening
epitope mutagenesis
Language English
License Copyright © 2019 Elsevier Inc. All rights reserved.
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Notes AUTHOR CONTRIBUTIONS
Conceptualization, T.K., M.H.D., and S.J.E.; Methodology, T.K., M.H.D., C.I.W., N.S.A., Z.C.H., H.K.L., and S.J.E.; Experimental Investigation, T.K., M.H.D., C.I.W., and N.S.A.; Resources, Z.C.H., H.K.L., and K.W.W.; Writing – Original Draft, T.K. and S.J.E.; Writing – Review & Editing, M.H.D., C.I.W., N.S.A., H.K.L., Z.C.H., and K.W.W.
OpenAccessLink http://www.cell.com/article/S0092867419307743/pdf
PMID 31398327
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PublicationDate 2019-08-08
PublicationDateYYYYMMDD 2019-08-08
PublicationDate_xml – month: 08
  year: 2019
  text: 2019-08-08
  day: 08
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle Cell
PublicationTitleAlternate Cell
PublicationYear 2019
Publisher Elsevier Inc
Publisher_xml – name: Elsevier Inc
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Snippet T cell recognition of specific antigens mediates protection from pathogens and controls neoplasias, but can also cause autoimmunity. Our knowledge of T cell...
T cell recognition of specific antigens mediates protection from pathogens and controls neoplasias, but can also cause autoimmunity. Our knowledge of T cell...
SourceID pubmedcentral
crossref
pubmed
elsevier
SourceType Open Access Repository
Aggregation Database
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StartPage 1016
SubjectTerms antigen discovery
Antigen Presentation - immunology
Antigens, Neoplasm - genetics
Antigens, Neoplasm - immunology
Blood Donors
CD8-Positive T-Lymphocytes - metabolism
epitope discovery
epitope mutagenesis
epitope screening
Epitopes, T-Lymphocyte - immunology
Female
Gene Knockout Techniques
Genes, MHC Class I - genetics
Genes, MHC Class I - immunology
Granzymes - metabolism
HEK293 Cells
HLA Antigens - genetics
HLA Antigens - immunology
Humans
immunological screening
Neoplasm Proteins - genetics
Neoplasm Proteins - immunology
off-target screening
peptide MHC recognition
Receptors, Antigen, T-Cell - immunology
T cell epitope
T cell screening
TCR epitope
TCR-specificity
Transduction, Genetic
Transfection
Title T-Scan: A Genome-wide Method for the Systematic Discovery of T Cell Epitopes
URI https://dx.doi.org/10.1016/j.cell.2019.07.009
https://www.ncbi.nlm.nih.gov/pubmed/31398327
https://pubmed.ncbi.nlm.nih.gov/PMC6939866
Volume 178
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