Pre-existing helminth infection impairs the efficacy of adjuvanted influenza vaccination in mice.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2022
Historique:
received: 09 09 2021
accepted: 21 03 2022
entrez: 31 3 2022
pubmed: 1 4 2022
medline: 15 4 2022
Statut: epublish

Résumé

The world health organization estimates that more than a quarter of the human population is infected with parasitic worms that are called helminths. Many helminths suppress the immune system of their hosts to prolong their survival. This helminth-induced immunosuppression "spills over" to unrelated antigens and can suppress the immune response to vaccination against other pathogens. Indeed, several human studies have reported a negative correlation between helminth infections and responses to vaccinations. Using mice that are infected with the parasitic nematode Litomosoides sigmodontis as a model for chronic human filarial infections, we reported previously that concurrent helminth infection impaired the vaccination-induced protection against the human pathogenic 2009 pandemic H1N1 influenza A virus (2009 pH1N1). Vaccinated, helminth-infected mice produced less neutralizing, influenza-specific antibodies than vaccinated naïve control mice. Consequently helminth-infected and vaccinated mice were not protected against a challenge infection with influenza virus but displayed high virus burden in the lung and a transient weight loss. In the current study we tried to improve the vaccination efficacy using vaccines that are licensed for humans. We either introduced a prime-boost vaccination regimen using the non-adjuvanted anti-influenza vaccine Begripal or employed the adjuvanted influenza vaccine Fluad. Although both strategies elevated the production of influenza-specific antibodies and protected mice from the transient weight loss that is caused by an influenza challenge infection, sterile immunity was not achieved. Helminth-infected vaccinated mice still had high virus burden in the lung while non-helminth-infected vaccinated mice rapidly cleared the virus. In summary we demonstrate that basic improvements of influenza vaccination regimen are not sufficient to confer sterile immunity on the background of helminth-induced immunosuppression, despite amelioration of pathology i.e. weight loss. Our findings highlight the risk of failed vaccinations in helminth-endemic areas, especially in light of the ongoing vaccination campaign to control the COVID-19 pandemic.

Identifiants

pubmed: 35358281
doi: 10.1371/journal.pone.0266456
pii: PONE-D-21-29265
pmc: PMC8970517
doi:

Substances chimiques

Adjuvants, Immunologic 0
Antibodies, Viral 0
Influenza Vaccines 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0266456

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Wiebke Hartmann (W)

Section for Molecular Biology and Immunology, Helminth Immunology Group, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.

Marie-Luise Brunn (ML)

Section for Molecular Biology and Immunology, Helminth Immunology Group, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.

Nadine Stetter (N)

Section for Molecular Biology and Immunology, Helminth Immunology Group, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.

Gülsah Gabriel (G)

Research Department for Viral Zoonoses-One Health, Leibniz Institute for Experimental Virology, Hamburg, Germany.
Institute of Virology, University for Veterinary Medicine, Hanover, Germany.

Minka Breloer (M)

Section for Molecular Biology and Immunology, Helminth Immunology Group, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Department for Biology, University Hamburg, Hamburg, Germany.

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Classifications MeSH