Evidence map›Paper›PMID 30498494›Full record

ArticleFrontiers in immunology2018

CD180 Ligation Inhibits TLR7- and TLR9-Mediated Activation of Macrophages and Dendritic Cells Through the Lyn-SHP-1/2 Axis in Murine Lupus.

Yonghong Yang, Cuiling Wang, Panpan Cheng, Xiaobei Zhang, Xuehui Li, Yuan Hu, Feihong Xu, Feng Hong, Guanjun Dong, Huabao Xiong

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 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

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  17. Immune Characteristics of LYN in Tumor Microenvironment of Gliomas.Frontiers in cell and developmental biology · 2021
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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

10 authors at 3 institutions in 2 countries.

Yonghong YangInstitute of Immunology and Molecular Medicine, Jining Medical University, Jining, China.
Cuiling WangDepartment of Hematology, Affiliated Hospital of Jining Medical University, Jining, China.
Panpan ChengDepartment of Hematology, Affiliated Hospital of Jining Medical University, Jining, China.
Xiaobei ZhangDepartment of Central Laboratory, Affiliated Hospital of Jining Medical University, Jining, China.
Xuehui LiInstitute of Immunology and Molecular Medicine, Jining Medical University, Jining, China.
Yuan HuDepartment of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Feihong XuDepartment of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Feng HongDepartment of Central Laboratory, Affiliated Hospital of Jining Medical University, Jining, China.
Guanjun DongInstitute of Immunology and Molecular Medicine, Jining Medical University, Jining, China.
Huabao XiongDepartment of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Affiliated Hospital of Jining Medical University · CNIcahn School of Medicine at Mount Sinai · USJining Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Activation of TLR7 and TLR9 by endogenous RNA- or DNA-containing ligands, respectively, can lead to hyper-activation of immune cells, including macrophages and DCs, subsequently contributes to the pathogenesis of SLE. CD180, a TLR-like protein, is specifically involved in the development and activation of immune cells. Our previous study and others have reported that CD180-negative B cells are dramatically increased in SLE patients and responsible for the production of auto-antibodies. However, the mode of CD180 expression on macrophages and DCs in SLE remains unclear and the role of CD180 on regulating TLR7- and TLR9-mediated activation of macrophages and DCs are largely unknown. In the present study, we found that the percentages of CD180-negative macrophages and DCs were both increased in SLE patients and lupus-prone MRL/

Indexed as

AnimalsAntigens, CDCell LineDendritic CellsDisease Models, AnimalFemaleHumansLupus Erythematosus, SystemicMacrophagesMembrane GlycoproteinsMiceMice, Inbred C57BLMice, Inbred MRL lprSignal TransductionToll-Like Receptor 7Toll-Like Receptor 9Antigens, CDLy78 protein, mouseMembrane GlycoproteinsTlr7 protein, mouseTlr9 protein, mouseToll-Like Receptor 7Toll-Like Receptor 9CD180DCsmacrophageSLETLR

Identifiers

PMID30498494
PMCPMC6249336
OpenAlexW2900811071

What OpenQuestion holds

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LicenceCC BY
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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.