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 |
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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. |
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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 |
AuthorAffiliation_xml | – name: 7 Lead Contact – name: 2 Department of Genetics, Harvard University Medical School, Boston, MA, USA – name: 5 Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Department of Immunobiology, Harvard Medical School, Boston, MA 02115, USA – name: 6 Departments of Surgery, Immunology, and Pathology, Duke University Medical Center, 571 Research Drive, Suite 433, Box 2606, Durham, NC 27710, USA – name: 4 Departments of Surgery and Pathology, Duke University Medical Center, 571 Research Drive, Suite 433, Box 2606, Durham, NC 27710, USA – name: 1 Division of Genetics, Department of Medicine, Howard Hughes Medical Institute, Brigham and Women’s Hospital, Boston, MA 02115, USA – name: 3 Department of Pathology, Massachusetts General Hospital, Boston, MA, USA |
Author_xml | – sequence: 1 givenname: Tomasz surname: Kula fullname: Kula, Tomasz organization: Division of Genetics, Department of Medicine, Howard Hughes Medical Institute, Brigham and Women’s Hospital, Boston, MA 02115, USA – sequence: 2 givenname: Mohammad H. surname: Dezfulian fullname: Dezfulian, Mohammad H. organization: Division of Genetics, Department of Medicine, Howard Hughes Medical Institute, Brigham and Women’s Hospital, Boston, MA 02115, USA – sequence: 3 givenname: Charlotte I. surname: Wang fullname: Wang, Charlotte I. organization: Division of Genetics, Department of Medicine, Howard Hughes Medical Institute, Brigham and Women’s Hospital, Boston, MA 02115, USA – sequence: 4 givenname: Nouran S. surname: Abdelfattah fullname: Abdelfattah, Nouran S. organization: Division of Genetics, Department of Medicine, Howard Hughes Medical Institute, Brigham and Women’s Hospital, Boston, MA 02115, USA – sequence: 5 givenname: Zachary C. surname: Hartman fullname: Hartman, Zachary C. organization: Departments of Surgery and Pathology, Duke University Medical Center, 571 Research Drive, Suite 433, Box 2606, Durham, NC 27710, USA – sequence: 6 givenname: Kai W. surname: Wucherpfennig fullname: Wucherpfennig, Kai W. organization: Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Department of Immunobiology, Harvard Medical School, Boston, MA 02115, USA – sequence: 7 givenname: Herbert Kim surname: Lyerly fullname: Lyerly, Herbert Kim organization: Departments of Surgery, Immunology, and Pathology, Duke University Medical Center, 571 Research Drive, Suite 433, Box 2606, Durham, NC 27710, USA – sequence: 8 givenname: Stephen J. surname: Elledge fullname: Elledge, Stephen J. email: selledge@genetics.med.harvard.edu organization: Division of Genetics, Department of Medicine, Howard Hughes Medical Institute, Brigham and Women’s Hospital, Boston, MA 02115, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31398327$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Copyright | 2019 Elsevier Inc. Copyright © 2019 Elsevier Inc. All rights reserved. |
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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 |
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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. |
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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... |
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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 |
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