Spike-directed vaccination elicits robust spike-specific T-cell response, including to mutant strains.


Journal

Cytotherapy
ISSN: 1477-2566
Titre abrégé: Cytotherapy
Pays: England
ID NLM: 100895309

Informations de publication

Date de publication:
01 2022
Historique:
received: 24 05 2021
revised: 23 06 2021
accepted: 09 07 2021
pubmed: 7 9 2021
medline: 12 1 2022
entrez: 6 9 2021
Statut: ppublish

Résumé

Although most studies describing coronavirus disease 2019 vaccine responses have focused on antibodies, there is increasing evidence that T cells play a critical role. Here the authors evaluated T-cell responses in seronegative donors before and after vaccination to define responses to the severe acute respiratory syndrome coronavirus 2 reference strain as well as to mutations in the variant strains Alpha/B.1.1.7 and Beta/B.1.351. The authors observed enhanced T-cell responses to reference and variant spike strains post-vaccination.

Identifiants

pubmed: 34483067
pii: S1465-3249(21)00741-6
doi: 10.1016/j.jcyt.2021.07.006
pmc: PMC8411349
pii:
doi:

Substances chimiques

Antibodies, Neutralizing 0
Antibodies, Viral 0
COVID-19 Vaccines 0
Spike Glycoprotein, Coronavirus 0

Types de publication

Journal Article Research Support, N.I.H., Intramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

10-15

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of Competing Interest CL, MDK, CRYC and CMB have intellectual property related to developing T-cell therapies for infectious diseases, including SARS-CoV-2.

Auteurs

Maja Stanojevic (M)

Program for Cell Enhancement and Technologies for Immunotherapy, Children's National Medical Center, Washington, DC, USA.

Ashley Geiger (A)

Program for Cell Enhancement and Technologies for Immunotherapy, Children's National Medical Center, Washington, DC, USA.

Brita Ostermeier (B)

Institute for Biomedical Sciences, George Washington University, Washington, DC, USA.

Danielle Sohai (D)

Program for Cell Enhancement and Technologies for Immunotherapy, Children's National Medical Center, Washington, DC, USA.

Christopher Lazarski (C)

Program for Cell Enhancement and Technologies for Immunotherapy, Children's National Medical Center, Washington, DC, USA.

Haili Lang (H)

Program for Cell Enhancement and Technologies for Immunotherapy, Children's National Medical Center, Washington, DC, USA.

Mariah Jensen-Wachspress (M)

Program for Cell Enhancement and Technologies for Immunotherapy, Children's National Medical Center, Washington, DC, USA.

Kathleen Webber (K)

Program for Cell Enhancement and Technologies for Immunotherapy, Children's National Medical Center, Washington, DC, USA.

Peter Burbelo (P)

National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland, USA.

Jeffrey Cohen (J)

National Institute of Allergy and Infectious Disease, National Institutes of Health, Bethesda, Maryland, USA.

Michael D Keller (MD)

Program for Cell Enhancement and Technologies for Immunotherapy, Children's National Medical Center, Washington, DC, USA.

Catherine M Bollard (CM)

Program for Cell Enhancement and Technologies for Immunotherapy, Children's National Medical Center, Washington, DC, USA. Electronic address: cbollard@childrensnational.org.

Conrad Russell Y Cruz (CRY)

Program for Cell Enhancement and Technologies for Immunotherapy, Children's National Medical Center, Washington, DC, USA. Electronic address: ccruz@childrensnational.org.

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Classifications MeSH