Evidence map›Paper›PMID 23046133›Full record

ReviewImmunological reviews2012

Pentraxins and Fc receptors.

Jinghua Lu, Kristopher D Marjon, Carolyn Mold, Terry W Du Clos, Peter D Sun

Open access · greenAbstract readReview
In one paragraph

Review in Immunological reviews, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

47 citing papers in PubMed, 99 citations in OpenAlex.

  1. Article
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  6. Review
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  8. Article
  9. C-reactive protein impairs immune response of CD8Journal for immunotherapy of cancer · 2023
    Article
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  15. Observational
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  17. Review
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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

5 authors at 4 institutions in 1 country.

Jinghua LuStructural Immunology Section, Laboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA.
Kristopher D Marjon
Carolyn Mold
Terry W Du Clos
Peter D Sun
University of New Mexico · USNational Institute of Allergy and Infectious Diseases · USNational Institutes of Health · USRaymond G. Murphy VA Medical Center · US

Funding

UNM HSC Clinical and Translational Science CenterUL1TR001449 · NCATS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI CAMPEN, MATTHEW J, PANDHI, NANCY · 2015 to 2024
$36.9M
University of New Mexico Clinical and Translational Science CenterUL1TR000041 · NCATS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI LARSON, RICHARD S · 2012 to 2014
$9.8M
Structural Mechanism of B cell receptor and complement activationZIAAI000853 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI SUN, PETER D. · 2009 to 2022
$5.3M
Biology of Infectious Diseases &InflammationT32AI007538 · NIAID · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Michelle A Ozbun · 1998 to 2026
$5.2M
Structural Mechanism of B cell receptor and complement activationZ01AI000853 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI SUN, PETER D. · 1999 to 2008
$594k
C-Reactive Protein Binding to CD89: Structure and FunctionR21AI085414 · NIAID · BIOMEDICAL RESEARCH INSTITUTE OF NEW MEX · PI DU CLOS, TERRY W · 2010 to 2011
$299k
Intramural NIH HHS Z01 AI000853NCATS NIH HHS UL1 TR000041NCATS NIH HHS UL1 TR001449NIAID NIH HHS R21 AI085414NIAID NIH HHS R21AI085414.NIAID NIH HHS T32 AI007538
6 · The paper itself

Abstract

Pentraxins are innate pattern recognition molecules whose major function is to bind microbial pathogens or cellular debris during infection and inflammation and, by doing so, contribute to the clearance of necrotic cells as well as pathogens through complement activations. Fc receptors are the cellular mediators of antibody functions. Although conceptually separated, both pentraxins and antibodies are important factors in controlling acute and chronic inflammation and infections. In recent years, increasing experimental evidence suggests a direct link between the innate pentraxins and humoral Fc receptors. Specifically, both human and mouse pentraxins recognize major forms of Fc receptors in solution and on cell surfaces with affinities similar to antibodies binding to their low affinity Fc receptors. Like immune complex, pentraxin aggregation and opsonization of pathogen result in Fc receptor and macrophage activation. The recently published crystal structure of human serum amyloid P (SAP) in complex with FcγRIIA further illustrated similarities to antibody recognition. These recent findings implicate a much broader role than complement activation for pentraxins in immunity. This review summarizes the structural and functional work that bridge the innate pentraxins and the adaptive Fc receptor functions. In many ways, pentraxins can be regarded as innate antibodies.

Indexed as

Adaptive ImmunityAnimalsAntibodiesAntigens, BacterialComplement ActivationC-Reactive ProteinHumansImmunity, InnateInflammationMiceModels, MolecularProtein BindingProtein Structure, TertiaryReceptors, IgGSerum Amyloid P-ComponentAntibodiesAntigens, BacterialC-Reactive ProteinFc gamma receptor IIAReceptors, IgGSerum Amyloid P-Component

Identifiers

PMID23046133
PMCPMC3471383
OpenAlexW2066286504

What OpenQuestion holds

Textmetadata
LicenceTDM
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.