Evidence map›Paper›PMID 30348950›Full record

ArticleCell death & disease2018

Azithromycin promotes alternatively activated macrophage phenotype in systematic lupus erythematosus via PI3K/Akt signaling pathway.

Jie Wang, Lin Xie, Shangshang Wang, Jinran Lin, Jun Liang, Jinhua Xu

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

40 citing papers in PubMed, 72 citations in OpenAlex.

  1. Erythromycin inhibits the differentiation of NCRJournal of thoracic disease · 2026
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  4. Plasma Exosomal LncRNA XIST Impairs CD4Journal of inflammation research · 2026
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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

6 authors at 2 institutions in 1 country.

Jie WangDepartment of Dermatology, Huashan Hospital, Fudan University, Shanghai, China.
Lin XieDepartment of Dermatology, Huashan Hospital, Fudan University, Shanghai, China.
Shangshang WangDepartment of Dermatology, Huashan Hospital, Fudan University, Shanghai, China.
Jinran LinDepartment of Dermatology, Huashan Hospital, Fudan University, Shanghai, China.
Jun LiangDepartment of Dermatology, Huashan Hospital, Fudan University, Shanghai, China. Liangjun1976@medmail.com.cn.
Jinhua XuDepartment of Dermatology, Huashan Hospital, Fudan University, Shanghai, China. xjhhsyy@163.com.
Fudan University · CNHuashan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alternatively activated macrophages have been reported to be helpful to alleviate systematic lupus erythematosus (SLE), and azithromycin could serve as an immunomodulator by promoting alternatively activated macrophage phenotype. However, the effect of azithromycin in SLE and the involved mechanism remain undetermined. The aim of this study is to characterize azithromycin and the underlying mechanism contributing to SLE therapy. First, we compared monocytes from SLE patients and matched healthy donors, and found monocytes from SLE patients exhibited more CD14

Indexed as

AdolescentAdultAnimalsAzithromycinCell LineDown-RegulationFemaleHumansInterleukin-10Interleukin-1betaLupus Erythematosus, SystemicMacrophagesMaleMembrane GlycoproteinsMiceMice, Inbred BALB CAzithromycinInterleukin-10Interleukin-1betaMembrane GlycoproteinsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTumor Necrosis Factor-alpha

Identifiers

PMID30348950
PMCPMC6197274
OpenAlexW2896860424

What OpenQuestion holds

Textmetadata
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.