Evidence map›Paper›PMID 35126381›Full record

ArticleFrontiers in immunology2021

TLR7 Signaling Shapes and Maintains Antibody Diversity Upon Virus-Like Particle Immunization.

Xinyue Chang, Pascal Krenger, Caroline C Krueger, Lisha Zha, Jiami Han, Alexander Yermanos, Salony Roongta, Mona O Mohsen, Annette Oxenius, Monique Vogel and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

26 citing papers in PubMed, 42 citations in OpenAlex.

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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

11 authors at 5 institutions in 3 countries.

Xinyue ChangDepartment of Rheumatology & Immunology, University Hospital Bern, Bern, Switzerland.
Pascal KrengerDepartment of Rheumatology & Immunology, University Hospital Bern, Bern, Switzerland.
Caroline C KruegerDepartment of Rheumatology & Immunology, University Hospital Bern, Bern, Switzerland.
Lisha ZhaInternational Immunology Centre, Anhui Agricultural University, Hefei, China.
Jiami HanDepartment of Biosystems Science and Engineering, Eidgenössische Technische Hochschule (ETH), Zürich, Basel, Switzerland.
Alexander YermanosDepartment of Biosystems Science and Engineering, Eidgenössische Technische Hochschule (ETH), Zürich, Basel, Switzerland.
Salony RoongtaDepartment of Rheumatology & Immunology, University Hospital Bern, Bern, Switzerland.
Mona O MohsenDepartment of Rheumatology & Immunology, University Hospital Bern, Bern, Switzerland.
Annette OxeniusInstitute of Microbiology, Eidgenössische Technische Hochschule Zürich, Zurich, Switzerland.
Monique VogelDepartment of Rheumatology & Immunology, University Hospital Bern, Bern, Switzerland.
Martin F BachmannDepartment of Rheumatology & Immunology, University Hospital Bern, Bern, Switzerland.
University Hospital of Bern · CHUniversity of Bern · CHETH Zurich · CHAnhui Agricultural University · CNUniversity of Geneva · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Virus-like particles (VLPs) are used in different marketed vaccines and are able to induce potent antibody responses. The innate pattern recognition receptors TLR7/8 recognize single stranded (ss) RNA naturally packaged into some VLPs and have been shown to enhance the production of IgG antibodies upon immunization. Here we demonstrate that, upon immunization with RNA-loaded bacteriophage-derived VLP Qβ, TLR7 signaling accelerates germinal center formation, promotes affinity/avidity maturation of VLP-specific IgG and isotype switching to IgG2b/2c. These findings extrapolated to antigens displayed on Qβ; as Fel d 1, the major cat allergen, chemically attached to Qβ also induced higher affinity/avidity IgG2b/2c antibodies in a TLR7-dependent fashion. Chimeric mice lacking TLR7-expression exclusively in B cells demonstrated that the enhanced IgG responses were driven by a B cell intrinsic mechanism. Importantly, deep sequencing of the BCR repertoire of antigen-specific B cells demonstrated higher diversity in mice with TLR7 signaling in B cells, suggesting that TLR7-signaling drives BCR repertoire development and diversity. Furthermore, the current data demonstrate that high levels of clonal diversity are reached early in the response and maintained by TLR7 signaling. In conclusion, TLR7 signaling enhances levels and quality of IgG antibodies, and this finding has major implications for vaccine design.

Indexed as

Signal TransductionAnimalsAntibodies, ViralAntibody DiversityB-LymphocytesGerminal CenterGlycoproteinsHost-Pathogen InteractionsImmunizationImmunoglobulin GImmunophenotypingMiceReceptors, Antigen, B-CellRecombinant ProteinsToll-Like Receptor 7Vaccines, Virus-Like ParticleAntibodies, ViralFel d 1 protein, Felis domesticusGlycoproteinsImmunoglobulin GReceptors, Antigen, B-CellRecombinant ProteinsToll-Like Receptor 7Vaccines, Virus-Like ParticleB cell receptor repertoireFel d 1hypermutationQβ-VLPTLR7

Identifiers

PMID35126381
PMCPMC8807482
OpenAlexW4205216773

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.