Evidence map›Paper›PMID 23053513›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2012

FcγRIIb on liver sinusoidal endothelium clears small immune complexes.

Latha P Ganesan, Jonghan Kim, Yun Wu, Sudhasri Mohanty, Gary S Phillips, Daniel J Birmingham, John M Robinson, Clark L Anderson

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 105 papers.

0numbers the graph read from it
0cells of the map it votes in
105citing papers in PubMed
5.7field-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

105 citing papers in PubMed, 163 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. The Scavenger Function of LSECs, a Regulator of Liver Diseases.Current issues in molecular biology · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. FcγRIIB functions as an IgG transporter in the mammary gland.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. A First-in-Class mAb (BI-1607) Targeting FcγRIIB: Preclinical Data and First-in-Human Studies in Patients with HER2-Positive Advanced Solid Tumors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review

45 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

8 authors at 2 institutions in 1 country.

Latha P GanesanDepartment of Internal Medicine, The Ohio State University, Columbus, OH 43210, USA.
Jonghan Kim
Yun Wu
Sudhasri Mohanty
Gary S Phillips
Daniel J Birmingham
John M Robinson
Clark L Anderson
The Ohio State University · USHarvard University · US

Funding

Immune Complex Elimination by Sinusoid Endothelial FcgRIIb: Mechanism and DiseaseR01AR066330 · NIAMS · OHIO STATE UNIVERSITY · PI ANDERSON, CLARK L, GANESAN, LATHA PRABHA · 2014 to 2018
$1.7M
IGG PLACENTAL TRANSPORT: ENDOTHELIAL CAVEOLAER01HD038764 · NICHD · OHIO STATE UNIVERSITY · PI ROBINSON, JOHN MITCHELL · 2000 to 2004
$1.7M
NIAMS NIH HHS R01 AR066330NICHD NIH HHS R01 HD038764NICHD NIH HHS R01 HD38764
6 · The paper itself

Abstract

It has long been known that the ITIM-bearing IgG Fc receptor (FcγRIIb, RIIb) is expressed on liver sinusoidal endothelial cells (LSEC) and that the liver is the major site of small immune complex (SIC) clearance. Thus, we proposed that RIIb of LSEC eliminates blood-borne SIC, thereby controlling immune complex-mediated autoimmune disease. Testing this hypothesis, we found most RIIb of the mouse, fully three-quarters, to be expressed in liver. Moreover, most (90%) liver RIIb was expressed in LSEC, the remainder in Kupffer cells. An absent FcRγ in LSEC implied that RIIb is the sole FcγR expressed. Testing the capacity of liver RIIb to clear blood-borne SIC, we infused mice intravenously with radio-iodinated SIC made of OVA and rabbit IgG anti-OVA. Tracking decay of SIC from the blood, we found the RIIb knockout strain to be severely deficient in eliminating SIC compared with the wild-type strain, terminal half-lives being 6 and 1.5 h, respectively. RIIb on LSEC, a major scavenger, keeps SIC blood concentrations low and minimizes pathologic deposition of inflammatory immune complex.

Indexed as

AnimalsAntigen-Antibody ComplexChlorocebus aethiopsCOS CellsEndotheliumKupffer CellsLiverMaleMiceMice, Inbred BALB CMice, KnockoutReceptors, IgGAntigen-Antibody ComplexFcgr2b protein, mouseReceptors, IgG

Identifiers

PMID23053513
PMCPMC4381350
OpenAlexW2119008186

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.