Evidence map›Paper›PMID 27340679›Full record

ArticleJournal of immunology research2016

A Fusion Protein Consisting of the Vaccine Adjuvant Monophosphoryl Lipid A and the Allergen Ovalbumin Boosts Allergen-Specific Th1, Th2, and Th17 Responses In Vitro.

Stefan Schülke, Lothar Vogel, Ann-Christine Junker, Kay-Martin Hanschmann, Adam Flaczyk, Stefan Vieths, Stephan Scheurer

Open access · goldAbstract read
In one paragraph

Article in Journal of immunology research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

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  12. Adjuvants for allergy immunotherapeutics.Human vaccines & immunotherapeutics · 2017
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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

7 authors at 1 institution in 1 country.

Stefan SchülkeVice President's Research Group 1: Molecular Allergology, Paul-Ehrlich-Institut, Langen, Hessen, Germany.ORCID 0000-0002-9674-5116
Lothar VogelDivision of Allergology, Paul-Ehrlich-Institut, 63225 Langen, Germany.
Ann-Christine JunkerVice President's Research Group 1: Molecular Allergology, Paul-Ehrlich-Institut, Langen, Hessen, Germany.ORCID 0000-0001-7600-4639
Kay-Martin HanschmannDivision of Microbiology, Paul-Ehrlich-Institut, 63225 Langen, Germany.
Adam FlaczykVice President's Research Group 1: Molecular Allergology, Paul-Ehrlich-Institut, Langen, Hessen, Germany.ORCID 0000-0002-9799-3170
Stefan ViethsVice President's Research Group 1: Molecular Allergology, Paul-Ehrlich-Institut, Langen, Hessen, Germany.
Stephan ScheurerVice President's Research Group 1: Molecular Allergology, Paul-Ehrlich-Institut, Langen, Hessen, Germany.ORCID 0000-0002-2859-562X
Paul Ehrlich Institut · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background. The detoxified TLR4-ligand Monophosphoryl Lipid A (MPLA) is the first approved TLR-agonist used as adjuvant in licensed vaccines but has not yet been explored as part of conjugated vaccines. Objective. To investigate the immune-modulating properties of a fusion protein consisting of MPLA and Ovalbumin (MPLA : Ova). Results. MPLA and Ova were chemically coupled by stable carbamate linkage. MPLA : Ova was highly pure without detectable product-related impurities by either noncoupled MPLA or Ova. Light scattering analysis revealed MPLA : Ova to be aggregated. Stimulation of mDC and mDC : DO11.10 CD4(+) TC cocultures showed a stronger activation of both mDC and Ova-specific DO11.10 CD4(+) TC by MPLA : Ova compared to the mixture of both components. MPLA : Ova induced both strong proinflammatory (IL-1β, IL-6, and TNF-α) and anti-inflammatory (IL-10) cytokine responses from mDCs while also boosting allergen-specific Th1, Th2, and Th17 cytokine secretion. Conclusion. Conjugation of MPLA and antigen enhanced the immune response compared to the mixture of both components. Due to the nonbiased boost of Ova-specific Th2 and Th17 responses while also inducing Th1 responses, this fusion protein may not be a suitable vaccine candidate for allergy treatment but may hold potential for the treatment of other diseases that require a strong stimulation of the host's immune system (e.g., cancer).

Indexed as

Adjuvants, ImmunologicAllergensCoculture TechniquesCytokinesHumansLipid AOvalbuminRecombinant Fusion ProteinsTh17 CellsTh1 CellsTh2 CellsVaccinesAdjuvants, ImmunologicAllergensCytokinesLipid Amonophosphoryl lipid AOvalbuminRecombinant Fusion ProteinsVaccines

Identifiers

PMID27340679
PMCPMC4908266
OpenAlexW2410501542

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.