Persistent Antibody Clonotypes Dominate the Serum Response to Influenza over Multiple Years and Repeated Vaccinations.


Journal

Cell host & microbe
ISSN: 1934-6069
Titre abrégé: Cell Host Microbe
Pays: United States
ID NLM: 101302316

Informations de publication

Date de publication:
13 Mar 2019
Historique:
received: 16 07 2018
revised: 02 11 2018
accepted: 18 01 2019
pubmed: 24 2 2019
medline: 9 11 2019
entrez: 24 2 2019
Statut: ppublish

Résumé

Humans are repeatedly exposed to influenza virus via infections and vaccinations. Understanding how multiple exposures and pre-existing immunity impact antibody responses is essential for vaccine development. Given the recent prevalence of influenza H1N1 A/California/7/2009 (CA09), we examined the clonal composition and dynamics of CA09 hemagglutinin (HA)-reactive IgG repertoire over 5 years in a donor with multiple influenza exposures. The anti-CA09 HA polyclonal response in this donor comprised 24 persistent antibody clonotypes, accounting for 72.6% ± 10.0% of the anti-CA09 HA repertoire over 5 years. These persistent antibodies displayed higher somatic hypermutation relative to transient serum antibodies detected at one time point. Additionally, persistent antibodies predominantly demonstrated cross-reactivity and potent neutralization toward a phylogenetically distant H5N1 A/Vietnam/1203/2004 (VT04) strain, a feature correlated with HA stem recognition. This analysis reveals how "serological imprinting" impacts responses to influenza and suggests that once elicited, cross-reactive antibodies targeting the HA stem can persist for years.

Identifiants

pubmed: 30795981
pii: S1931-3128(19)30048-4
doi: 10.1016/j.chom.2019.01.010
pmc: PMC6417944
mid: NIHMS1519399
pii:
doi:

Substances chimiques

Antibodies, Viral 0
H1N1 virus hemagglutinin 0
Hemagglutinin Glycoproteins, Influenza Virus 0
Immunoglobulin G 0
Influenza Vaccines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

367-376.e5

Subventions

Organisme : European Research Council
ID : 670955
Pays : International
Organisme : NIAID NIH HHS
ID : P01 AI089618
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

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Auteurs

Jiwon Lee (J)

Department of Chemical Engineering, The University of Texas at Austin, Austin, TX 78712, USA.

Philipp Paparoditis (P)

Institute for Research in Biomedicine, Università della Svizzera Italiana, Bellinzona 6500, Switzerland; Institute of Microbiology, ETH Zürich, Zürich 8093, Switzerland.

Andrew P Horton (AP)

Center for Systems and Synthetic Biology, The University of Texas at Austin, Austin, TX 78712, USA.

Alexander Frühwirth (A)

Institute for Research in Biomedicine, Università della Svizzera Italiana, Bellinzona 6500, Switzerland.

Jonathan R McDaniel (JR)

Department of Chemical Engineering, The University of Texas at Austin, Austin, TX 78712, USA.

Jiwon Jung (J)

Department of Biomedical Engineering, The University of Texas at Austin, Austin, TX 78712, USA.

Daniel R Boutz (DR)

Center for Systems and Synthetic Biology, The University of Texas at Austin, Austin, TX 78712, USA.

Dania A Hussein (DA)

Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX 78712, USA.

Yuri Tanno (Y)

Department of Chemical Engineering, The University of Texas at Austin, Austin, TX 78712, USA.

Leontios Pappas (L)

Institute for Research in Biomedicine, Università della Svizzera Italiana, Bellinzona 6500, Switzerland.

Gregory C Ippolito (GC)

Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX 78712, USA.

Davide Corti (D)

Humabs BioMed, Bellinzona 6500, Switzerland.

Antonio Lanzavecchia (A)

Institute for Research in Biomedicine, Università della Svizzera Italiana, Bellinzona 6500, Switzerland; Institute of Microbiology, ETH Zürich, Zürich 8093, Switzerland.

George Georgiou (G)

Department of Chemical Engineering, The University of Texas at Austin, Austin, TX 78712, USA; Center for Systems and Synthetic Biology, The University of Texas at Austin, Austin, TX 78712, USA; Department of Biomedical Engineering, The University of Texas at Austin, Austin, TX 78712, USA; Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX 78712, USA. Electronic address: gg@che.utexas.edu.

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