Evidence map›Paper›PMID 31130948›Full record

ReviewFrontiers in immunology2019

Functional Roles of the IgM Fc Receptor in the Immune System.

Hiromi Kubagawa, Kazuhito Honjo, Naganari Ohkura, Shimon Sakaguchi, Andreas Radbruch, Fritz Melchers, Peter K Jani

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
6.0field-weighted citation impact, top 3% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 66 citations in OpenAlex.

  1. Pooled it
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  3. Review
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  8. Review
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  15. Review
  16. Article
  17. Structural basis for Fc receptor recognition of immunoglobulin M.Nature structural & molecular biology · 2023
    Article
  18. Multi-faceted immunoglobulin M meets its elusive receptor.Nature structural & molecular biology · 2023
    Article
  19. Article
  20. Review
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

7 authors at 3 institutions in 3 countries.

Hiromi KubagawaDeutsches Rheuma-Forschungszentrum, Berlin, Germany.
Kazuhito HonjoDepartment of Medicine, School of Medicine, University of Alabama at Birmingham, Birmingham, AL, United States.
Naganari OhkuraImmunology Frontier Research Center, Osaka University, Osaka, Japan.
Shimon SakaguchiImmunology Frontier Research Center, Osaka University, Osaka, Japan.
Andreas RadbruchDeutsches Rheuma-Forschungszentrum, Berlin, Germany.
Fritz MelchersDeutsches Rheuma-Forschungszentrum, Berlin, Germany.
Peter K JaniDeutsches Rheuma-Forschungszentrum, Berlin, Germany.
German Rheumatism Research Centre · DEOsaka University · JPUniversity of Alabama at Birmingham · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is now evident from studies of mice unable to secrete IgM that both non-immune "natural" and antigen-induced "immune" IgM are important for protection against pathogens and for regulation of immune responses to self-antigens. Since identification of its Fc receptor (FcμR) by a functional cloning strategy in 2009, the roles of FcμR in these IgM effector functions have begun to be explored. Unlike Fc receptors for switched Ig isotypes (e.g., FcγRs, FcεRs, FcαR, Fcα/μR, pIgR, FcRn), FcμR is selectively expressed by lymphocytes: B, T, and NK cells in humans and only B cells in mice. FcμR may have dual signaling ability: one through a potential as yet unidentified adaptor protein non-covalently associating with the FcμR ligand-binding chain via a His in transmembrane segment and the other through its own Tyr and Ser residues in the cytoplasmic tail. FcμR binds pentameric and hexameric IgM with a high avidity of ~10 nM in solution, but more efficiently binds IgM when it is attached to a membrane component via its Fab region on the same cell surface (

Indexed as

AnimalsAutoimmunityB-LymphocytesEpigenesis, GeneticHumansReceptors, FcT-Lymphocytes, Regulatoryimmunoglobulin M receptorReceptors, FcautoantibodyepigeneticsFcμRMott cellnatural IgMtolerance

Identifiers

PMID31130948
PMCPMC6509151
OpenAlexW2943161370

What OpenQuestion holds

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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.