Evidence map›Paper›PMID 35951003›Full record

ArticleClinical and experimental immunology2022

Elevated expression of TAM receptor tyrosine kinase in synovial fluid and synovial tissue of rheumatoid arthritis.

Li Zheng, Liling Xu, Fanlei Hu, Jimeng Xue, Mingxin Bai, Ranran Yao, Huaqun Zhu, Hua Zhong, Yin Su

Open access · bronzeAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Li ZhengDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Liling XuDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.ORCID 0000-0002-2095-0906
Fanlei HuDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Jimeng XueDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Mingxin BaiDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.ORCID 0000-0002-7031-3526
Ranran YaoDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Huaqun ZhuDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Hua ZhongDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.ORCID 0000-0002-5264-6407
Yin SuDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Peking University · CNShanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To investigate the expression and roles of TAM (Tyro3/Axl/Mer) receptor tyrosine kinases (TK) in synovial fluid and synovial tissue of patients with rheumatoid arthritis (RA). The expression of TAM TKs in the synovial fluid and synovial tissues of RA and osteoarthritis (OA) patients was measured by ELISA and immunohistochemistry. The relationships between soluble TAM TKs (sTAM TKs) levels and the clinical features, laboratory parameters and disease activity were analyzed in RA. The concentrations of sTAM TK in the synovial fluids of RA patients were increased in comparison to those of OA patients. Compared with OA patients, the expression of membrane Tyro3 TK (mTyro3 TK) and mMer TK in RA patient synovial tissue were significantly increased, which may partly explain the possible mechanism of elevated levels of sTAM TK in RA patient synovial fluid. sAxl TK levels were decreased in RA patients under sulfasalazine treatment and elevated in patients under Iguratimod treatment. Furthermore, sTyro3 TK levels were positively correlated with erythrocyte sedimentation rate (ESR) and negatively correlated with white blood cells (WBCs), red blood cells (RBCs), and hemoglobin (HB) in RA patients. The levels of sMer TK were positively associated with disease duration and rheumatoid factor (RF) and negatively correlated with HB, complement 3 (C3), and C4. Taken together, TAM TKs might be involved in RA synovial tissue inflammation.

Indexed as

Arthritis, RheumatoidOsteoarthritisComplement C3HumansReceptor Protein-Tyrosine KinasesRheumatoid FactorSulfasalazineSynovial FluidSynovial MembraneTyrosineComplement C3Receptor Protein-Tyrosine KinasesRheumatoid FactorSulfasalazineTyrosineclinical featuresrheumatoid arthritissynovial fluidsynoviocytesTAM receptor tyrosine kinase

Identifiers

PMID35951003
PMCPMC9521663
OpenAlexW4291006642

What OpenQuestion holds

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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.