Evidence map›Paper›PMID 36707501›Full record

ArticleCell death & disease2023

Interleukin-18-primed human umbilical cord-mesenchymal stem cells achieve superior therapeutic efficacy for severe viral pneumonia via enhancing T-cell immunosuppression.

Yan Liao, Zeqin Fu, Yinfu Huang, Shiduo Wu, Zhen Wang, Shaotang Ye, Weijie Zeng, Guifang Zeng, Duanduan Li, Yulin Yang and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Immune cell disorder in viral pneumonia.Journal of translational medicine · 2026
    Review
  4. The Roles of Interleukin-18 in Inflammation and Autoimmune Disease.Clinical reviews in allergy & immunology · 2026
    Review
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  6. Review
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  8. Article
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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

18 authors at 4 institutions in 1 country.

Yan Liao *Shenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Zeqin Fu *Shenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Yinfu Huang *Shenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Shiduo Wu *Shenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Zhen WangCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, 510642, China.
Shaotang YeCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, 510642, China.
Weijie ZengShenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Guifang ZengShenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Duanduan LiShenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Yulin YangShenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Ke PeiShenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Jian YangShenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Zhiwei HuShenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Xiao LiangShenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Junyuan HuShenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China. hujunyuan2020@163.com.
Muyun LiuNational-Local Associated Engineering Laboratory for Personalized Cell Therapy, Shenzhen, 518054, China. liumuyun@nlelpct.com.
Juan JinDepartment of Nephrology, the First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Traditional Chinese Medicine), Hangzhou, 310000, China. lang_018@163.com.
Cheguo CaiShenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China. cheguo_cai@whu.edu.cn.ORCID 0000-0002-3712-1696
Beike Biotechnology (China) · CNSouth China Agricultural University · CNCell Technology (China) · CNZhejiang Chinese Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coronavirus disease 2019 (COVID-19) treatments are still urgently needed for critically and severely ill patients. Human umbilical cord-mesenchymal stem cells (hUC-MSCs) infusion has therapeutic benefits in COVID-19 patients; however, uncertain therapeutic efficacy has been reported in severe patients. In this study, we selected an appropriate cytokine, IL-18, based on the special cytokine expression profile in severe pneumonia of mice induced by H1N1virus to prime hUC-MSCs in vitro and improve the therapeutic effect of hUC-MSCs in vivo. In vitro, we demonstrated that IL-18-primed hUC-MSCs (IL18-hUCMSC) have higher proliferative ability than non-primed hUC-MSCs (hUCMSCcon). In addition, VCAM-1, MMP-1, TGF-β1, and some chemokines (CCL2 and CXCL12 cytokines) are more highly expressed in IL18-hUCMSCs. We found that IL18-hUCMSC significantly enhanced the immunosuppressive effect on CD3

Indexed as

COVID-19Mesenchymal Stem CellsMesenchymal Stem Cell TransplantationPneumonia, ViralAnimalsCytokinesHumansImmunosuppression TherapyInterleukin-18MiceT-LymphocytesUmbilical CordCytokinesInterleukin-18

Identifiers

PMID36707501
PMCPMC9883134
OpenAlexW4318318154

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.