Evidence map›Paper›PMID 34938294›Full record

ArticleFrontiers in immunology2021

B Cell Intrinsic STING Signaling Is Not Required for Autoreactive Germinal Center Participation.

Kenneth Green, Thomas R Wittenborn, Cecilia Fahlquist-Hagert, Ewa Terczynska-Dyla, Nina van Campen, Lisbeth Jensen, Line Reinert, Rune Hartmann, Søren R Paludan, Søren E Degn

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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

5 citing papers in PubMed, 8 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

10 authors at 2 institutions in 2 countries.

Kenneth GreenDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Thomas R WittenbornDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Cecilia Fahlquist-HagertDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Ewa Terczynska-DylaDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Nina van CampenDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Lisbeth JensenDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Line ReinertDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Rune HartmannDepartment of Molecular Biology and Genetics, Aarhus University, Aarhus, Denmark.
Søren R PaludanDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Søren E DegnDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Aarhus University · DKRadboud University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Germinal centers (GCs) are induced microanatomical structures wherein B cells undergo affinity maturation to improve the quality of the antibody response. Although GCs are crucial to appropriate humoral responses to infectious challenges and vaccines, many questions remain about the molecular signals driving B cell participation in GC responses. The cyclic GMP-AMP synthase (cGAS)-stimulator of interferon genes (STING) pathway is an important mediator of type I interferon and proinflammatory cytokine responses during infection and cellular stress. Recent studies have reported important roles for STING in B cell responses, including an impact on GC B cells and downstream antibody responses, which could have great consequences for vaccine design and understanding STING-associated interferonopathies. GCs are also involved in untoward reactions to autoantigens in a plethora of autoimmune disorders, and it is generally thought that these responses coopt the mechanisms used in foreign antigen-directed GCs. Here, we set out to investigate the importance of the cGAS-STING pathway in autoreactive B cell responses. In a direct competition scenario in a murine mixed bone marrow chimera model of autoreactive GCs, we find that B cell intrinsic deficiency of cGAS, STING, or the type I interferon receptor IFNAR, does not impair GC participation, whereas Toll-like receptor (TLR)-7 deficiency mediates a near-complete block. Our findings suggest that physiological B cell responses are strictly sustained by signals linked to BCR-mediated endocytosis. This wiring of B cell signals may enable appropriate antibody responses, while at the same time restricting aberrant antibody responses during infections and in autoimmune or autoinflammatory settings.

Indexed as

AutoimmunitySignal TransductionAnimalsBiomarkersB-LymphocytesCell LineCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseFlow CytometryGerminal CenterHumansImmunohistochemistryMembrane ProteinsMiceMice, KnockoutMice, TransgenicMutationBiomarkerscGAS protein, mouseCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseMembrane ProteinsNucleotidyltransferasesReceptor, Interferon alpha-betaSting1 protein, mouseSTING ProteinToll-Like Receptor 7autoimmunityautoreactivityB cellscGASgerminal centersIFNARSTINGTLR7

Identifiers

PMID34938294
PMCPMC8685402
OpenAlexW4200497931

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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.