Evidence map›Paper›PMID 37901251›Full record

ReviewFrontiers in immunology2023

Mitochondrial antiviral signaling protein: a potential therapeutic target in renal disease.

Meng Wu, Zhiyin Pei, Guangfeng Long, Hongbing Chen, Zhanjun Jia, Weiwei Xia

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.6field-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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. CircARID1B Promotes MPPCell biochemistry and biophysics · 2025
    Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Understanding the impact ofFrontiers in molecular biosciences · 2024
    Review
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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.

Meng WuDepartment of Clinical Laboratory, Children's Hospital of Nanjing Medical University, Nanjing, China.
Zhiyin PeiDepartment of Clinical Laboratory, Children's Hospital of Nanjing Medical University, Nanjing, China.
Guangfeng LongDepartment of Clinical Laboratory, Children's Hospital of Nanjing Medical University, Nanjing, China.
Hongbing ChenDepartment of Clinical Laboratory, Children's Hospital of Nanjing Medical University, Nanjing, China.
Zhanjun JiaDepartment of Nephrology, Children's Hospital of Nanjing Medical University, Nanjing, China.
Weiwei XiaDepartment of Clinical Laboratory, Children's Hospital of Nanjing Medical University, Nanjing, China.
Second Affiliated Hospital of Nanjing Medical University · CNNanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondrial antiviral signaling protein (MAVS) is a key innate immune adaptor on the outer mitochondrial membrane that acts as a switch in the immune signal transduction response to viral infections. Some studies have reported that MAVS mediates NF-κB and type I interferon signaling during viral infection and is also required for optimal NLRP3 inflammasome activity. Recent studies have reported that MAVS is involved in various cancers, systemic lupus erythematosus, kidney diseases, and cardiovascular diseases. Herein, we summarize the structure, activation, pathophysiological roles, and MAVS-based therapies for renal diseases. This review provides novel insights into MAVS's role and therapeutic potential in the pathogenesis of renal diseases.

Indexed as

Kidney DiseasesSignal TransductionHumansImmunity, InnateNF-kappa BNF-kappa Binflammationinnate immuneMAVSNLRP3renal disease

Identifiers

PMID37901251
PMCPMC10602740
OpenAlexW4387580850

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.