Resolving SARS-CoV-2 CD4


Journal

Cell reports. Medicine
ISSN: 2666-3791
Titre abrégé: Cell Rep Med
Pays: United States
ID NLM: 101766894

Informations de publication

Date de publication:
16 08 2022
Historique:
received: 18 11 2021
revised: 08 05 2022
accepted: 24 06 2022
pubmed: 17 7 2022
medline: 20 8 2022
entrez: 16 7 2022
Statut: ppublish

Résumé

The current strategy to detect immunodominant T cell responses focuses on the antigen, employing large peptide pools to screen for functional cell activation. However, these approaches are labor and sample intensive and scale poorly with increasing size of the pathogen peptidome. T cell receptors (TCRs) recognizing the same epitope frequently have highly similar sequences, and thus, the presence of large sequence similarity clusters in the TCR repertoire likely identify the most public and immunodominant responses. Here, we perform a meta-analysis of large, publicly available single-cell and bulk TCR datasets from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-infected individuals to identify public CD4

Identifiants

pubmed: 35841887
pii: S2666-3791(22)00233-6
doi: 10.1016/j.xcrm.2022.100697
pmc: PMC9247234
pii:
doi:

Substances chimiques

Epitopes 0
Receptors, Antigen, T-Cell 0

Types de publication

Journal Article Meta-Analysis Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

100697

Subventions

Organisme : NIAID NIH HHS
ID : F32 AI157296
Pays : United States

Commentaires et corrections

Type : UpdateOf

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests P.B. and A.S. are consultants of Miltenyi Biotec, who own IP rights concerning parts of the ARTE technology. P.G.T. has consulted and/or received honoraria and travel support from Illumina, Johnson and Johnson, and 10X Genomics. P.G.T. serves on the Scientific Advisory Board of Immunoscape and Cytoagents. The authors have applied for patents covering some aspects of these studies.

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Auteurs

Mikhail V Pogorelyy (MV)

Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38103, USA.

Elisa Rosati (E)

Institute of Clinical Molecular Biology, Christian-Albrecht University of Kiel, Kiel, Germany; Institute of Immunology, Christian-Albrecht University of Kiel, Kiel, Germany.

Anastasia A Minervina (AA)

Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38103, USA.

Robert C Mettelman (RC)

Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38103, USA.

Alexander Scheffold (A)

Institute of Immunology, Christian-Albrecht University of Kiel, Kiel, Germany.

Andre Franke (A)

Institute of Clinical Molecular Biology, Christian-Albrecht University of Kiel, Kiel, Germany.

Petra Bacher (P)

Institute of Clinical Molecular Biology, Christian-Albrecht University of Kiel, Kiel, Germany; Institute of Immunology, Christian-Albrecht University of Kiel, Kiel, Germany. Electronic address: p.bacher@ikmb.uni-kiel.de.

Paul G Thomas (PG)

Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38103, USA. Electronic address: paul.thomas@stjude.org.

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