Evidence map›Paper›PMID 35656386›Full record

ReviewCytokine: X2022

Progress of exosome research in systemic lupus erythematosus.

Jie Shen, Mengyu Zhang, Meiyu Peng

Open access · hybridAbstract readReview
In one paragraph

Review in Cytokine: X, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
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

3 authors at 1 institution in 1 country.

Jie ShenWeifang Medical University, Weifang 261053, China.
Mengyu ZhangWeifang Medical University, Weifang 261053, China.
Meiyu PengWeifang Medical University, Weifang 261053, China.
Weifang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) is a global chronic autoimmune disease that invades most organs of the body, with kidney injury being the most prominent feature. Exosomes are extracellular vesicles that carry a variety of proteins, lipids and genetic material, participate in the exchange of local and intersystem information, and play an important immunoregulatory role in a variety of autoimmune diseases. At the same time, the use of exosomes as disease biomarkers and drug delivery carriers also shows great application prospects. This article reviews current progress in the application of exosomes in the pathogenesis, diagnosis and treatment of SLE.

Indexed as

CfDNA, Circulating free DNADiagnostic roleExosomesHMGB1, High mobility group box 1ImmunomodulationLN, Lupus nephritisMicroribonucleic acidMiRNAs, Microribonucleic acidsMSC, Mesenchymal stem cells (MSC)PAMPs, Pathogen-associated molecular patternsPDCs, Plasmacytoid dendritic cellsSLE, Systemic lupus erythematosusSystemic lupus erythematosusTherapeutic potentialTLR, Recombinant Toll Like ReceptorTreg, Regulatory T cells

Identifiers

PMID35656386
PMCPMC9151726
OpenAlexW4281251536

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.