Evidence map›Paper›PMID 9653099›Full record

ArticleThe Journal of experimental medicine1998

Reversal of proinflammatory responses by ligating the macrophage Fcgamma receptor type I.

F S Sutterwala, G J Noel, P Salgame, D M Mosser

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 124 papers.

0numbers the graph read from it
0cells of the map it votes in
124citing papers in PubMed
14.9field-weighted citation impact, top 1% 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

124 citing papers in PubMed, 324 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Review
  6. Regulatory macrophages in solid organ xenotransplantation.Korean journal of transplantation · 2023
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Macrophage polarization in intestinal inflammation and gut homeostasis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2020
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

64 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

4 authors at 1 institution in 1 country.

F S SutterwalaDepartment of Microbiology and Immunology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140, USA.
G J Noel
P Salgame
D M Mosser
Cornell University · US

Funding

MACROPHAGE RECEPTORS FOR LEISHMANIAR01AI024313 · NIAID · UNIVERSITY OF MARYLAND COLLEGE PK CAMPUS · PI MOSSER, DAVID M · 1993 to 2002
$734k
MACROPHAGE RECEPTORS FOR LEISHMANIAR21AI024313 · NIAID · TEMPLE UNIVERSITY · PI MOSSER, DAVID M · 1997 to 1997
–
THE MACROPHAGE RECEPTORS FOR LEISHMANIAR29AI024313 · NIAID · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI MOSSER, DAVID M · 1988 to 1991
–
NIAID NIH HHS AI24313
6 · The paper itself

Abstract

Macrophages can respond to a variety of infectious and/or inflammatory stimuli by secreting an array of proinflammatory cytokines, the overproduction of which can result in shock or even death. In this report, we demonstrate that ligation of macrophage Fcgamma receptors (FcgammaR) can lead to a reversal of macrophage proinflammatory responses by inducing an upregulation of interleukin (IL)-10, with a reciprocal inhibition of IL-12 production. IL-10 upregulation was specific to FcgammaR ligation, since the ligation of the Mac-1 receptor did not alter IL-10 production. The identification of the specific FcgammaR subtype responsible for IL-10 upregulation was determined in gene knockout mice. Macrophages from mice lacking the FcR gamma chain, which is required for assembly and signaling by FcgammaRI and FcgammaRIII, failed to upregulate IL-10 in response to immune complexes. However, mice lacking either the FcgammaRII or the FcgammaRIII were fully capable of upregulating IL-10 production, implicating FcgammaRI in this process. The biological consequences of FcgammaRI ligation were determined in both in vitro and in vivo models of inflammation and sepsis. In all of the models tested, the ligation of FcgammaR promoted the production of IL-10 and inhibited the secretion of IL-12. This reciprocal alteration in the pattern of macrophage cytokine production illustrates a potentially important role for FcgammaR-mediated clearance in suppressing macrophage proinflammatory responses.

Indexed as

AnimalsCytokinesInflammationInterleukin-10Interleukin-12LipopolysaccharidesMacrophage-1 AntigenMacrophagesMiceMice, Inbred BALB CMice, KnockoutReceptors, IgGUp-RegulationCytokinesInterleukin-10Interleukin-12LipopolysaccharidesMacrophage-1 AntigenReceptors, IgG

Identifiers

PMID9653099
PMCPMC2525554
OpenAlexW2115848892

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.