| Literature DB >> 31398327 |
Tomasz Kula1, Mohammad H Dezfulian1, Charlotte I Wang2, Nouran S Abdelfattah1, Zachary C Hartman3, Kai W Wucherpfennig4, Herbert Kim Lyerly5, Stephen J Elledge6.
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.Entities:
Keywords: T cell epitope; T cell screening; TCR epitope; TCR-specificity; antigen discovery; epitope discovery; epitope mutagenesis; epitope screening; immunological screening; off-target screening; peptide MHC recognition
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Year: 2019 PMID: 31398327 PMCID: PMC6939866 DOI: 10.1016/j.cell.2019.07.009
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582