Evidence map›Paper›PMID 35911733›Full record

ArticleFrontiers in immunology2022

Type I Interferons Promote Germinal Centers Through B Cell Intrinsic Signaling and Dendritic Cell Dependent Th1 and Tfh Cell Lineages.

Madelene W Dahlgren, Adam W Plumb, Kristoffer Niss, Katharina Lahl, Søren Brunak, Bengt Johansson-Lindbom

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

32 citing papers in PubMed, 38 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

6 authors at 3 institutions in 2 countries.

Madelene W DahlgrenImmunology Section, Lund University, Lund, Sweden.
Adam W PlumbDepartment of Health Technology, Technical University of Denmark, Lyngby, Denmark.
Kristoffer NissNovo Nordisk Foundation Center for Protein Research, University of Copenhagen, Copenhagen, Denmark.
Katharina LahlImmunology Section, Lund University, Lund, Sweden.
Søren BrunakDepartment of Health Technology, Technical University of Denmark, Lyngby, Denmark.
Bengt Johansson-LindbomImmunology Section, Lund University, Lund, Sweden.
Technical University of Denmark · DKLund University · SENovo Nordisk Foundation · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type I interferons (IFNs) are essential for antiviral immunity, appear to represent a key component of mRNA vaccine-adjuvanticity, and correlate with severity of systemic autoimmune disease. Relevant to all, type I IFNs can enhance germinal center (GC) B cell responses but underlying signaling pathways are incompletely understood. Here, we demonstrate that a succinct type I IFN response promotes GC formation and associated IgG subclass distribution primarily through signaling in cDCs and B cells. Type I IFN signaling in cDCs, distinct from cDC1, stimulates development of separable Tfh and Th1 cell subsets. However, Th cell-derived IFN-γ induces T-bet expression and IgG2c isotype switching in B cells prior to this bifurcation and has no evident effects once GCs and

Indexed as

Interferon Type IT Follicular Helper CellsCell LineageDendritic CellsGerminal CenterImmunoglobulin GmRNA VaccinesVaccines, SyntheticImmunoglobulin GInterferon Type ImRNA VaccinesVaccines, Syntheticantibody responsesgerminal center (GC) B cellsIgG subclass antibodiesTfh cellsTh1 cellsType I Interferons

Identifiers

PMID35911733
PMCPMC9326081
OpenAlexW4285087012

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.