Evidence map›Paper›PMID 17312177›Full record

Trial reportJournal of immunology (Baltimore, Md. : 1950)2007

Expression profile of FcgammaRIIb on leukocytes and its dysregulation in systemic lupus erythematosus.

Kaihong Su, Hengxuan Yang, Xinrui Li, Xiaoli Li, Andrew W Gibson, John M Cafardi, Tong Zhou, Jeffrey C Edberg, Robert P Kimberly

Open access · bronzeAbstract readClinical TrialComparative Study
In one paragraph

Trial report in Journal of immunology (Baltimore, Md. : 1950), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed
10.4field-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

94 citing papers in PubMed, 173 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. B Cell Aberrance in Lupus: the Ringleader and the Solution.Clinical reviews in allergy & immunology · 2022
    Review
  12. Sodium houttuyfonate effectively treats acute pulmonary infection ofFrontiers in cellular and infection microbiology · 2022
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Inhibition of B cell activation followingJournal of translational autoimmunity · 2021
    Article
  18. The Neutrophil: The Underdog That Packs a Punch in the Fight against Cancer.International journal of molecular sciences · 2020
    Review
  19. Article
  20. Review

34 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

9 authors at 1 institution in 1 country.

Kaihong SuDivision of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Hengxuan Yang
Xinrui Li
Xiaoli Li
Andrew W Gibson
John M Cafardi
Tong Zhou
Jeffrey C Edberg
Robert P Kimberly
University of Alabama at Birmingham · US

Funding

Zevalin Radioimmunotherapy Using a Modified TreatmentM01RR000032 · NCRR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI RICH, ROBERT R. · 1985 to 2008
$23.6M
Program Project in the Genetics of SLEP01AR049084 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BROWN, ELIZABETH E · 2002 to 2012
$12.7M
ROS Modulation of Innate and Adaptive Immunity in RAP30AR048311 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MOUNTZ, JOHN D · 2001 to 2017
$9.5M
MONONUCLEAR PHAGOCYTE FUNCTION IN IMMUNOLOGIC DISEASESR01AR033062 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KIMBERLY, ROBERT P. · 1986 to 2010
$3.8M
SYSTEMIC VASCULITIS--HOST FACTORS IN TISSUE INJURYR01AR042476 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI EDBERG, JEFFREY C · 1994 to 2008
$2.4M
Population Genetics Analysis Program: Immunity to Vaccines/InfectionsN01AI40068 · NIAID · PI , · 2007 to 2007
$834k
Tissue-Specific Expression and Regulation of the Inhibitory lgG Fc ReceptorR03AR054530 · NIAMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI SU, KAIHONG · 2007 to 2009
$214k
POPULATION GENETICS ANALYSIS PROGRAM IMMUNITY TO VACCINES/INFECTION-266040068N01AI040068 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KASLOW, RICHARD ALAN · 2006 to 2006
–
NCRR NIH HHS M01 RR000032NCRR NIH HHS M01 RR 00032NIAID NIH HHS N01 AI040068NIAID NIH HHS N01 AI 40068NIAMS NIH HHS P01 AR049084NIAMS NIH HHS P01 AR 49084NIAMS NIH HHS P30 AR048311NIAMS NIH HHS P30 AR 48311NIAMS NIH HHS R01 AR033062NIAMS NIH HHS R01 AR042476NIAMS NIH HHS R01 AR 33062NIAMS NIH HHS R01 AR 42476NIAMS NIH HHS R03 AR054530
6 · The paper itself

Abstract

FcgammaRIIb (CD32B, Online Mendelian Inheritance in Man 604590), an IgG FcR with a tyrosine-based inhibitory motif, plays a critical role in the balance of tolerance and autoimmunity in murine models. However, the high degree of homology between FcgammaRIIb and FcgammaRIIa in humans and the lack of specific Abs to differentiate them have hampered study of the normal expression profile of FcgammaRIIb and its potential dysregulation in autoimmune diseases such as systemic lupus erythematosus (SLE). Using our newly developed anti-FcgammaRIIb mAb 4F5 which does not react with FcgammaRIIa, we found that FcgammaRIIb is expressed on the cell surface of circulating B lymphocytes, monocytes, neutrophils, myeloid dendritic cells (DCs), and at very low levels on plasmacytoid DCs from some donors. Normal donors with the less frequent 2B.4 promoter haplotype have higher FcgammaRIIb expression on monocytes, neutrophils, and myeloid DCs similar to that reported for B lymphocytes, indicating that FcgammaRIIb expression on both myeloid and lymphoid cells is regulated by the naturally occurring regulatory single nucleotide polymorphisms in the FCGR2B promoter. FcgammaRIIb expression in normal controls is up-regulated on memory B lymphocytes compared with naive B lymphocytes. In contrast, in active SLE, FcgammaRIIb is significantly down-regulated on both memory and plasma B lymphocytes compared with naive and memory/plasma B lymphocytes from normals. Similar down-regulation of FcgammaRIIb on myeloid-lineage cells in SLE was not seen. Our studies demonstrate the constitutive regulation of FcgammaRIIb by natural gene polymorphisms and the acquired dysregulation in SLE autoimmunity, which may identify opportunities for using this receptor as a therapeutic target.

Indexed as

Gene Expression RegulationPolymorphism, Single NucleotidePromoter Regions, GeneticAnimalsAntigens, CDAutoimmunityFemaleHumansLeukocytesLupus Erythematosus, SystemicMaleMiceReceptors, IgGAntigens, CDFc gamma receptor IIAFCGR2B protein, humanReceptors, IgG

Identifiers

PMID17312177
PMCPMC2824439
OpenAlexW1871780345

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.