Evidence map›Paper›PMID 26643820›Full record

ArticleVirology journal2015

Matrix-M™ adjuvation broadens protection induced by seasonal trivalent virosomal influenza vaccine.

Freek Cox, Eirikur Saeland, Matthijs Baart, Martin Koldijk, Jeroen Tolboom, Liesbeth Dekking, Wouter Koudstaal, Karin Lövgren Bengtsson, Jaap Goudsmit, Katarina Radošević

Open access · goldAbstract read
In one paragraph

Article in Virology journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 3 countries.

Freek CoxPresent Address: Infectious Diseases and Vaccines Therapeutic area, Janssen Research and Development, Pharmaceutical companies of Johnson and Johnson, Leiden, The Netherlands. FCox@its.jnj.com.
Eirikur SaelandPresent Address: Infectious Diseases and Vaccines Therapeutic area, Janssen Research and Development, Pharmaceutical companies of Johnson and Johnson, Leiden, The Netherlands. Esaeland@its.jnj.com.
Matthijs BaartPresent Address: Infectious Diseases and Vaccines Therapeutic area, Janssen Research and Development, Pharmaceutical companies of Johnson and Johnson, Leiden, The Netherlands. MBaart@its.jnj.com.
Martin KoldijkPresent Address: Janssen Prevention Center, Center of Excellence of Janssen Research & Development, Janssen Pharmaceutical companies of Johnson and Johnson, Leiden, The Netherlands. MKoldijk@its.jnj.com.
Jeroen TolboomPresent Address: Infectious Diseases and Vaccines Therapeutic area, Janssen Research and Development, Pharmaceutical companies of Johnson and Johnson, Leiden, The Netherlands. JTolboom@its.jnj.com.
Liesbeth DekkingPresent Address: Infectious Diseases and Vaccines Therapeutic area, Janssen Research and Development, Pharmaceutical companies of Johnson and Johnson, Leiden, The Netherlands. LDekking@its.jnj.com.
Wouter KoudstaalPresent Address: Janssen Prevention Center, Center of Excellence of Janssen Research & Development, Janssen Pharmaceutical companies of Johnson and Johnson, Leiden, The Netherlands. WKoudsta@its.jnj.com.
Karin Lövgren BengtssonPresent Address: Novavax AB, Uppsala, Sweden. KLovgren@Novavax.com.
Jaap GoudsmitPresent Address: Janssen Prevention Center, Center of Excellence of Janssen Research & Development, Janssen Pharmaceutical companies of Johnson and Johnson, Leiden, The Netherlands. JGoudsmi@its.jnj.com.
Katarina RadoševićPresent Address: Sanofi, Global Biotherapeutics, Vitry-sur-Seine, France. K_Radosevic@hotmail.com.
Johnson & Johnson (Netherlands) · NLJanssen (Netherlands) · NLNovavax (Sweden) · SESanofi (France) · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInfluenza virus infections are responsible for significant morbidity worldwide and therefore it remains a high priority to develop more broadly protective vaccines. Adjuvation of current seasonal influenza vaccines has the potential to achieve this goal.

methodsTo assess the immune potentiating properties of Matrix-M™, mice were immunized with virosomal trivalent seasonal vaccine adjuvated with Matrix-M™. Serum samples were isolated to determine the hemagglutination inhibiting (HAI) antibody titers against vaccine homologous and heterologous strains. Furthermore, we assess whether adjuvation with Matrix-M™ broadens the protective efficacy of the virosomal trivalent seasonal vaccine against vaccine homologous and heterologous influenza viruses.

resultsMatrix-M™ adjuvation enhanced HAI antibody titers and protection against vaccine homologous strains. Interestingly, Matrix-M™ adjuvation also resulted in HAI antibody titers against heterologous influenza B strains, but not against the tested influenza A strains. Even though the protection against heterologous influenza A was induced by the adjuvated vaccine, in the absence of HAI titers the protection was accompanied by severe clinical scores and body weight loss. In contrast, in the presence of heterologous HAI titers full protection against the heterologous influenza B strain without any disease symptoms was obtained.

conclusionThe results of this study emphasize the promising potential of a Matrix-M™-adjuvated seasonal trivalent virosomal influenza vaccine. Adjuvation of trivalent virosomal vaccine does not only enhance homologous protection, but in addition induces protection against heterologous strains and thus provides overall more potent and broad protective immunity.

Indexed as

Adjuvants, ImmunologicAnimalsAntibodies, ViralBody WeightFemaleHemagglutination Inhibition TestsImmunity, HeterologousInfluenza VaccinesMice, Inbred BALB COrthomyxoviridaeOrthomyxoviridae InfectionsSeverity of Illness IndexVaccines, Virus-Like ParticleAdjuvants, ImmunologicAntibodies, ViralInfluenza VaccinesVaccines, Virus-Like Particle

Identifiers

PMID26643820
PMCPMC4672496
OpenAlexW2194742159

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.