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Abdulhaqq, S.* ; Ventura, A.B.* ; Reed, J.S.* ; Bashirova, A.A.* ; Bateman, K.B.* ; McDonald, E.* ; Wu, H.L.* ; Greene, J.M.* ; Schell, J.B.* ; Morrow, D.* ; Wisskirchen, K. ; Martin, J.N.* ; Deeks, S.G.* ; Carrington, M.N.* ; Protzer, U. ; Früh, K.* ; Hansen, S.G.* ; Picker, L.J.* ; Sacha, J.B.* ; Bimber, B.N.*

Identification and characterization of antigen-specific CD8+ T cells using surface-trapped TNF-α and single-cell sequencing.

J. Immunol. 207, 2913-2921 (2021)
Postprint DOI
Open Access Green
CD8+ T cells are key mediators of antiviral and antitumor immunity. The isolation and study of Ag-specific CD8+ T cells, as well as mapping of their MHC restriction, has practical importance to the study of disease and the development of therapeutics. Unfortunately, most experimental approaches are cumbersome, owing to the highly variable and donor-specific nature of MHC-bound peptide/TCR interactions. Here we present a novel system for rapid identification and characterization of Ag-specific CD8+ T cells, particularly well suited for samples with limited primary cells. Cells are stimulated ex vivo with Ag of interest, followed by live cell sorting based on surface-trapped TNF-α. We take advantage of major advances in single-cell sequencing to generate full-length sequence data from the paired TCR α- and β-chains from these Ag-specific cells. The paired TCR chains are cloned into retroviral vectors and used to transduce donor CD8+ T cells. These TCR transductants provide a virtually unlimited experimental reagent, which can be used for further characterization, such as minimal epitope mapping or identification of MHC restriction, without depleting primary cells. We validated this system using CMV-specific CD8+ T cells from rhesus macaques, characterizing an immunodominant Mamu-A1*002:01-restricted epitope. We further demonstrated the utility of this system by mapping a novel HLA-A*68:02-restricted HIV Gag epitope from an HIV-infected donor. Collectively, these data validate a new strategy to rapidly identify novel Ags and characterize Ag-specific CD8+ T cells, with applications ranging from the study of infectious disease to immunotherapeutics and precision medicine.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Cd8(+) T-cells; Lymphocyte Response; Flow-cytometry; Receptor; Epitope; Expression; Transformation; Progression; Populations; Enrichment
ISSN (print) / ISBN 0022-1767
e-ISSN 1550-6606
Zeitschrift Journal of Immunology
Quellenangaben Band: 207, Heft: 12, Seiten: 2913-2921 Artikelnummer: , Supplement: ,
Verlag American Association of Immunologists
Verlagsort 9650 Rockville Pike, Bethesda, Md 20814 Usa
Begutachtungsstatus Peer reviewed
Förderungen Center for AIDS Research Network of Integrated Systems
National Institutes of Health Office of the Director Grant
German Research Foundation
U.S. Department of Defense Grant
Frederick National Laboratory for Cancer Research
University of California, San Francisco/Gladstone Institute of Virology and Immunology Center for AIDS Research
National Institute of Allergy and Infectious Diseases