Evidence map›Paper›PMID 20566717›Full record

ArticleThe Journal of experimental medicine2010

Type I IFN enhances follicular B cell contribution to the T cell-independent antibody response.

Cristina L Swanson, Timothy J Wilson, Pamela Strauch, Marco Colonna, Roberta Pelanda, Raul M Torres

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 108 papers.

0numbers the graph read from it
0cells of the map it votes in
108citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

108 citing papers in PubMed, 164 citations in OpenAlex.

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  16. Aberrant METTL1-mediated tRNA mNature communications · 2024
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48 more citing papers are in PubMed but not listed here.

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 1 country.

Cristina L SwansonIntegrated Department of Immunology, University of Colorado, Denver, CO 80206, USA.
Timothy J Wilson
Pamela Strauch
Marco Colonna
Roberta Pelanda
Raul M Torres
University of Colorado Denver · USWashington University in St. Louis · USNational Jewish Health · US

Funding

Chemokine response in B cell development and functionR01AI052157 · NIAID · UNIVERSITY OF COLORADO DENVER · PI TORRES, RAUL MARTIN · 2002 to 2017
$5.4M
Tolerance in Polyclonal and Oligoclonal Immune SystemsR01AI052310 · NIAID · UNIVERSITY OF COLORADO DENVER · PI PELANDA, ROBERTA · 2003 to 2017
$5.0M
Molecular Mechanisms of Immune ToleranceT32AI074491 · NIAID · NATIONAL JEWISH HEALTH · PI CAMBIER, JOHN C, PELANDA, ROBERTA · 2009 to 2023
$4.1M
Marginal Zone B Cell Response to HIVR21AI078468 · NIAID · UNIVERSITY OF COLORADO DENVER · PI TORRES, RAUL MARTIN · 2008 to 2009
$424k
Tolerance in Polyclonal and Oligoclonal Immune SystemsR56AI052310 · NIAID · NATIONAL JEWISH HEALTH · PI PELANDA, ROBERTA · 2007 to 2007
$363k
NIAID NIH HHS AI052157NIAID NIH HHS AI052310NIAID NIH HHS AI078468NIAID NIH HHS R01 AI052157NIAID NIH HHS R01 AI052310NIAID NIH HHS R21 AI078468NIAID NIH HHS R56 AI052310
6 · The paper itself

Abstract

Humoral immunity to viruses and encapsulated bacteria is comprised of T cell-independent type 2 (TI-2) antibody responses that are characterized by rapid antibody production by marginal zone and B1 B cells. We demonstrate that toll-like receptor (TLR) ligands influence the TI-2 antibody response not only by enhancing the overall magnitude but also by skewing this response to one that is dominated by IgG isotypes. Importantly, TLR ligands facilitate this response by inducing type I interferon (IFN), which in turn elicits rapid and significant amounts of antigen-specific IgG2c predominantly from FO (follicular) B cells. Furthermore, we show that although the IgG2c antibody response requires B cell-autonomous IFN-alpha receptor signaling, it is independent of B cell-intrinsic TLR signaling. Thus, innate signals have the capacity to enhance TI-2 antibody responses by promoting participation of FO B cells, which then elaborate effective IgG anti-pathogen antibodies.

Indexed as

AnimalsAntibody AffinityAntibody FormationAntigensAntigens, CDAntigens, Differentiation, T-LymphocyteB-LymphocytesCD69 AntigensEpitopesFicollImmunoglobulin Class SwitchingInterferon-alphaKineticsLectins, C-TypeLymph NodesMiceAntigensAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensEpitopesFicollIgG2c receptorInterferon-alphaLectins, C-TypePoly I-CReceptors, Antigen, B-CellReceptors, IgGTLR3 protein, mouseToll-Like Receptor 3

Identifiers

PMID20566717
PMCPMC2901065
OpenAlexW2108671666

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.