Evidence map›Paper›PMID 35402422›Full record

ArticleFrontiers in medicine2022

Human Amnion Epithelial Cells and Their Derived Exosomes Alleviate Sepsis-Associated Acute Kidney Injury

Dongxuan Chi, Ying Chen, Chengang Xiang, Weijian Yao, Hui Wang, Xizi Zheng, Damin Xu, Nan Li, Min Xie, Suxia Wang and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
3.3field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it, 22 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

13 authors at 4 institutions in 1 country.

Dongxuan ChiDepartment of Critical Care Medicine, Peking University First Hospital, Beijing, China.
Ying ChenRenal Division, Peking University First Hospital, Beijing, China.
Chengang XiangRenal Division, Peking University First Hospital, Beijing, China.
Weijian YaoRenal Division, Peking University First Hospital, Beijing, China.
Hui WangLaboratory of Electron Microscopy, Pathological Center, Peking University First Hospital, Beijing, China.
Xizi ZhengRenal Division, Peking University First Hospital, Beijing, China.
Damin XuRenal Division, Peking University First Hospital, Beijing, China.
Nan LiDepartment of Critical Care Medicine, Peking University First Hospital, Beijing, China.
Min XieDepartment of Critical Care Medicine, Peking University First Hospital, Beijing, China.
Suxia WangLaboratory of Electron Microscopy, Pathological Center, Peking University First Hospital, Beijing, China.
Gang LiuRenal Division, Peking University First Hospital, Beijing, China.
Shuangling LiDepartment of Critical Care Medicine, Peking University First Hospital, Beijing, China.
Li YangRenal Division, Peking University First Hospital, Beijing, China.
Peking University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNPeking University First Hospital · CNMinistry of Education of the People's Republic of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sepsis is characterized by organ dysfunction resulting from a patient's dysregulated response to infection. Sepsis-associated acute kidney injury (S-AKI) is the most frequent complication contributing to the morbidity and mortality of sepsis. The prevention and treatment of S-AKI remains a significant challenge worldwide. In the recent years, human amnion epithelial cells (hAECs) have drawn much attention in regenerative medicine, yet the therapeutic efficiency of hAECs in S-AKI has not been evaluated. Methods: Septic mice were induced by cecal ligation and puncture (CLP) operation. hAECs and their derived exosomes (EXOs) were injected into the mice Results: hAECs decreased the mortality of CLP mice, ameliorated septic injury in the kidney, and improved kidney function. More precisely, hAECs suppressed systemic inflammation and maintained the renal endothelial integrity in septic animals. EXOs from hAECs exhibited similar renal protective effects as their parental cells. EXOs maintained endothelial cell adhesion junction Conclusion: Our results indicate that hAECs and their derived EXOs may ameliorate S-AKI

Indexed as

acute kidney injuryendothelial dysfunctionexosomeshAECssepsisstem cell therapy

Identifiers

PMID35402422
PMCPMC8989462
OpenAlexW4220959073

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.