An Antigenic Thrift-Based Approach to Influenza Vaccine Design.

antigenic drift antigenic thrift evolutionary theory influenza vaccination vaccine

Journal

Vaccines
ISSN: 2076-393X
Titre abrégé: Vaccines (Basel)
Pays: Switzerland
ID NLM: 101629355

Informations de publication

Date de publication:
16 Jun 2021
Historique:
received: 16 04 2021
revised: 04 06 2021
accepted: 05 06 2021
entrez: 2 7 2021
pubmed: 3 7 2021
medline: 3 7 2021
Statut: epublish

Résumé

The antigenic drift theory states that influenza evolves via the gradual accumulation of mutations, decreasing a host's immune protection against previous strains. Influenza vaccines are designed accordingly, under the premise of antigenic drift. However, a paradox exists at the centre of influenza research. If influenza evolved primarily through mutation in multiple epitopes, multiple influenza strains should co-circulate. Such a multitude of strains would render influenza vaccines quickly inefficacious. Instead, a single or limited number of strains dominate circulation each influenza season. Unless additional constraints are placed on the evolution of influenza, antigenic drift does not adequately explain these observations. Here, we explore the constraints placed on antigenic drift and a competing theory of influenza evolution - antigenic thrift. In contrast to antigenic drift, antigenic thrift states that immune selection targets epitopes of limited variability, which constrain the variability of the virus. We explain the implications of antigenic drift and antigenic thrift and explore their current and potential uses in the context of influenza vaccine design.

Identifiants

pubmed: 34208489
pii: vaccines9060657
doi: 10.3390/vaccines9060657
pmc: PMC8235769
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : NIAID NIH HHS
ID : 75N93019C00076
Pays : United States

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Auteurs

Jai S Bolton (JS)

Peter Medawar Building for Pathogen Research, Oxford OX1 3SY, UK.
Department of Zoology, University of Oxford, Oxford OX1 3SZ, UK.

Hannah Klim (H)

Peter Medawar Building for Pathogen Research, Oxford OX1 3SY, UK.
Department of Zoology, University of Oxford, Oxford OX1 3SZ, UK.
Department of Philosophy, Future of Humanity Institute, University of Oxford, Oxford OX2 0DJ, UK.

Judith Wellens (J)

Peter Medawar Building for Pathogen Research, Oxford OX1 3SY, UK.
Nuffield Department of Medicine, University of Oxford, Oxford OX3 7BN, UK.
Translational Research in GastroIntestinal Disorders, University Hospitals Leuven, 3000 Leuven, Belgium.

Matthew Edmans (M)

Peter Medawar Building for Pathogen Research, Oxford OX1 3SY, UK.
Nuffield Department of Medicine, University of Oxford, Oxford OX3 7BN, UK.

Uri Obolski (U)

School of Public Health, Faculty of Medicine, Tel-Aviv University, Tel-Aviv 69978, Israel.
Porter School of Environment and Earth Sciences, Faculty of Exact Sciences, Tel-Aviv University, Tel-Aviv 69978, Israel.

Craig P Thompson (CP)

Peter Medawar Building for Pathogen Research, Oxford OX1 3SY, UK.
Department of Zoology, University of Oxford, Oxford OX1 3SZ, UK.

Classifications MeSH