Evidence map›Paper›PMID 29138852›Full record

ArticleMolecular medicine reports2018

Anti‑IL‑39 (IL‑23p19/Ebi3) polyclonal antibodies ameliorate autoimmune symptoms in lupus‑like mice.

Xiaoqian Wang, Yu Zhang, Zhiding Wang, Xiaoling Liu, Gaizhi Zhu, Gencheng Han, Guojiang Chen, Chunmei Hou, Tianxiao Wang, Beifen Shen and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

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  14. IL-39 acts as a friend to pancreatic cancer.Medical oncology (Northwood, London, England) · 2018
    Article
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

14 authors at 3 institutions in 1 country.

Xiaoqian WangLaboratory of Immunology, Institute of Basic Medical Sciences, Beijing 100850, P.R. China.
Yu ZhangLaboratory of Immunology, Institute of Basic Medical Sciences, Beijing 100850, P.R. China.
Zhiding WangLaboratory of Immunology, Institute of Basic Medical Sciences, Beijing 100850, P.R. China.
Xiaoling LiuLaboratory of Immunology, Institute of Basic Medical Sciences, Beijing 100850, P.R. China.
Gaizhi ZhuLaboratory of Immunology, Institute of Basic Medical Sciences, Beijing 100850, P.R. China.
Gencheng HanLaboratory of Immunology, Institute of Basic Medical Sciences, Beijing 100850, P.R. China.
Guojiang ChenLaboratory of Immunology, Institute of Basic Medical Sciences, Beijing 100850, P.R. China.
Chunmei HouLaboratory of Immunology, Institute of Basic Medical Sciences, Beijing 100850, P.R. China.
Tianxiao WangCollege of Pharmacy, Henan University, Kaifeng, Henan 475004, P.R. China.
Beifen ShenLaboratory of Immunology, Institute of Basic Medical Sciences, Beijing 100850, P.R. China.
Yan LiLaboratory of Immunology, Institute of Basic Medical Sciences, Beijing 100850, P.R. China.
He XiaoLaboratory of Immunology, Institute of Basic Medical Sciences, Beijing 100850, P.R. China.
Ning MaDepartment of Rheumatology, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Renxi WangLaboratory of Immunology, Institute of Basic Medical Sciences, Beijing 100850, P.R. China.
Institute of Basic Medical Sciences of the Chinese Academy of Medical SciencesHenan University · CNJilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The interleukin (IL)‑12 family cytokines have been examined as therapeutic targets in the treatment of several autoimmune diseases. Our previous study showed that a novel IL‑12 family cytokine, IL‑39 (IL‑23p19/Ebi3) mediates inflammation in lupus‑like mice. In the present study, the effect of anti‑mouse IL‑39 polyclonal antibodies on autoimmune symptoms in lupus‑like mice was investigated. Rabbit anti‑mouse IL‑39 polyclonal antibodies were produced by immunization with recombinant mouse IL‑39, and purified using protein A chromatography. These antibodies were subsequently used to treat lupus‑like mice. Flow cytometry, captured images, ELISA and H&E staining were used to determine the effect of anti‑IL‑39 polyclonal antibodies on inflammatory cells, autoantibody titers, proteinuria, infiltrating inflammatory cells and the structure of the glomerular region. The anti‑IL‑39 polyclonal antibodies effectively reduced the numbers of inflammatory cells, splenomegaly, autoantibody titers, proteinuria, infiltrating inflammatory cells, and restored the structure of the glomerular region in MRL/lpr mice. Taken together, these results suggested that anti‑IL‑39 polyclonal antibodies ameliorated autoimmune symptoms in lupus‑like mice. Therefore, IL‑39 may be used as a possible target for the treatment of systemic lupus erythematosus.

Indexed as

AnimalsAntibodiesAutoantibodiesDrug Evaluation, PreclinicalFemaleGlomerulonephritisImmunologic FactorsInterleukin-23 Subunit p19KidneyLupus Erythematosus, SystemicMice, TransgenicMinor Histocompatibility AntigensProteinuriaRabbitsReceptors, CytokineAntibodiesAutoantibodiesEbi3 protein, mouseImmunologic FactorsInterleukin-23 Subunit p19Minor Histocompatibility AntigensReceptors, Cytokine

Identifiers

PMID29138852
PMCPMC5780108
OpenAlexW2768335504

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.