Evidence map›Paper›PMID 29988500›Full record

ArticleFrontiers in immunology2018

Role of Hepatic Deposited Immunoglobulin G in the Pathogenesis of Liver Damage in Systemic Lupus Erythematosus.

Xiang Fang, Muhammad Haidar Zaman, Xuanxuan Guo, Huimin Ding, Changhao Xie, Xiaojun Zhang, Guo-Min Deng

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 2 institutions in 1 country.

Xiang FangKey Laboratory of Antibody Technology, National Health and Family Planning Commission, Nanjing Medical University, Nanjing, China.
Muhammad Haidar ZamanKey Laboratory of Antibody Technology, National Health and Family Planning Commission, Nanjing Medical University, Nanjing, China.
Xuanxuan GuoKey Laboratory of Antibody Technology, National Health and Family Planning Commission, Nanjing Medical University, Nanjing, China.
Huimin DingKey Laboratory of Antibody Technology, National Health and Family Planning Commission, Nanjing Medical University, Nanjing, China.
Changhao XieKey Laboratory of Antibody Technology, National Health and Family Planning Commission, Nanjing Medical University, Nanjing, China.
Xiaojun ZhangFirst affiliated Hospital of Nanjing Medical University, Nanjing, China.
Guo-Min DengKey Laboratory of Antibody Technology, National Health and Family Planning Commission, Nanjing Medical University, Nanjing, China.
Nanjing Medical University · CNNational Health and Family Planning Commission · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The onset of hepatic disorders in patients with systemic lupus erythematosus (SLE) is frequent; however, the etiology and liver pathogenesis of SLE remain unknown. In the present study, the role of hepatic deposited immunoglobulin G (IgG) in SLE-derived liver damage was investigated. From a retrospective analysis of the medical records of 404 patients with lupus and from experimental studies on mice models, we found that liver dysfunction is common in SLE and liver damage with IgG deposition spontaneously develops in lupus-prone mice. Liver injury was recreated in mice by injecting IgG from lupus serum intrahepatically. The inflammation intensity in the liver decreased with IgG depletion and the lupus IgG-induced liver inflammation in FcγRIII-deficient mice was comparatively low; while, inflammation was increased in FcγRIIb-deficient mice. Macrophages, Kupffer cells, natural killer cells, and their products, but not lymphocytes, are required for the initiation of SLE-associated liver inflammation. Blocking IgG signaling using a spleen tyrosine kinase (Syk) inhibitor suppressed the liver damage. Our findings provided evidence of spontaneously established liver damage in SLE. They also suggested that hepatic-deposited lupus IgG is an important pathological factor in the development of liver injury and that hepatic inflammation is regulated by the Syk signaling pathway. Thus, Syk inhibition might promote the development of a therapeutic strategy to control liver damage in patients with SLE.

Indexed as

hepatitisimmunoglobulin G depositioninnate immune cellsspleen tyrosine kinasesystemic lupus erythematosus

Identifiers

PMID29988500
PMCPMC6026631
OpenAlexW2808030514

What OpenQuestion holds

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LicenceCC BY
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.