SARS-CoV-2-specific peripheral T follicular helper cells correlate with neutralizing antibodies and increase during convalescence.


Journal

medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986

Informations de publication

Date de publication:
12 Oct 2020
Historique:
entrez: 14 10 2020
pubmed: 15 10 2020
medline: 15 10 2020
Statut: epublish

Résumé

T-cell immunity is likely to play a role in protection against SARS-CoV-2 by helping generate neutralizing antibodies. We longitudinally studied CD4 T-cell responses to the M, N, and S structural proteins of SARS-CoV-2 in 21 convalescent individuals. Within the first two months following symptom onset, a majority of individuals (81%) mount at least one CD4 T-cell response, and 48% of individuals mount detectable SARS-CoV-2-specific peripheral T follicular helper cells (pTfh, defined as CXCR5+PD1+ CD4 T cells). SARS-CoV-2-specific pTfh responses across all three protein specificities correlate with antibody neutralization with the strongest correlation observed for S protein-specific responses. When examined over time, pTfh responses increase in frequency and magnitude in convalescence, and robust responses with magnitudes greater than 5% were detected only at the second convalescent visit, an average of 38 days post-symptom onset. These data deepen our understanding of antigen-specific pTfh responses in SARS-CoV-2 infection, suggesting that M and N protein-specific pTfh may also assist in the development of neutralizing antibodies and that pTfh response formation may be delayed in SARS-CoV-2 infection.

Identifiants

pubmed: 33052359
doi: 10.1101/2020.10.07.20208488
pmc: PMC7553179
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NIAID NIH HHS
ID : F30 AI140829
Pays : United States

Commentaires et corrections

Type : UpdateIn

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Auteurs

Sushma Boppana (S)

Division of Infectious Diseases, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

Kai Qin (K)

Division of Infectious Diseases, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

Jacob K Files (JK)

Division of Infectious Diseases, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

Ronnie M Russell (RM)

Department of Medicine, University of Pennsylvania, Philadelphia, PA.
Department of Microbiology, University of Pennsylvania, Philadelphia, PA.

Regina Stoltz (R)

Department of Medicine, University of Pennsylvania, Philadelphia, PA.

Frederic Bibollet-Ruche (F)

Department of Medicine, University of Pennsylvania, Philadelphia, PA.
Department of Microbiology, University of Pennsylvania, Philadelphia, PA.

Anju Bansal (A)

Division of Infectious Diseases, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

Nathan Erdmann (N)

Division of Infectious Diseases, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

Beatrice H Hahn (BH)

Department of Medicine, University of Pennsylvania, Philadelphia, PA.
Department of Microbiology, University of Pennsylvania, Philadelphia, PA.

Paul Goepfert (P)

Division of Infectious Diseases, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

Classifications MeSH