Evidence map›Paper›PMID 33483751›Full record

ReviewCardiovascular research2021

An update on the roles of immune system-derived microRNAs in cardiovascular diseases.

Luke B Roberts, Puja Kapoor, Jane K Howard, Ajay M Shah, Graham M Lord

Open access · hybridAbstract readReview
In one paragraph

Review in Cardiovascular research, 2021. 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 33% 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, 16 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. MicroRNAs in T Cell-Immunotherapy.International journal of molecular sciences · 2022
    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

5 authors at 1 institution in 1 country.

Luke B RobertsSchool of Immunology and Microbial Sciences, King's College London, Great Maze Pond, London SE1 9RT, UK.ORCID 0000-0003-1143-304X
Puja KapoorSchool of Immunology and Microbial Sciences, King's College London, Great Maze Pond, London SE1 9RT, UK.ORCID 0000-0001-6027-1038
Jane K HowardSchool of Life Course Sciences, King's College London, Great Maze Pond, London SE1 9RT, UK.ORCID 0000-0003-2754-8300
Ajay M ShahSchool of Cardiovascular Medicine and Sciences, King's British Heart Foundation Centre, King's College London, 125 Coldharbour Lane, London SE5 9NU, UK.ORCID 0000-0002-6547-0631
Graham M LordSchool of Immunology and Microbial Sciences, King's College London, Great Maze Pond, London SE1 9RT, UK.ORCID 0000-0003-2069-4743
King's College London · GB

Funding

British Heart Foundation PG/12/36/29444British Heart Foundation PG/18/43/33688British Heart Foundation RE/18/2/34213Medical Research Council MR/K002996/1Medical Research Council MR/M003493/1Wellcome Trust 091009
6 · The paper itself

Abstract

Cardiovascular diseases (CVD) are a leading cause of human death worldwide. Over the past two decades, the emerging field of cardioimmunology has demonstrated how cells of the immune system play vital roles in the pathogenesis of CVD. MicroRNAs (miRNAs) are critical regulators of cellular identity and function. Cell-intrinsic, as well as cell-extrinsic, roles of immune and inflammatory cell-derived miRNAs have been, and continue to be, extensively studied. Several 'immuno-miRNAs' appear to be specifically expressed or demonstrate greatly enriched expression within leucocytes. Identification of miRNAs as critical regulators of immune system signalling pathways has posed the question of whether and how targeting these molecules therapeutically, may afford opportunities for disease treatment and/or management. As the field of cardioimmunology rapidly continues to advance, this review discusses findings from recent human and murine studies which contribute to our understanding of how leucocytes of innate and adaptive immunity are regulated-and may also regulate other cell types, via the actions of the miRNAs they express, in the context of CVD. Finally, we focus on available information regarding miRNA regulation of regulatory T cells and argue that targeted manipulation of miRNA regulated pathways in these cells may hold therapeutic promise for the treatment of CVD and associated risk factors.

Indexed as

Adaptive ImmunityImmunity, InnateAnimalsCardiovascular DiseasesCardiovascular SystemGene Expression RegulationHumansImmune SystemImmunotherapyMicroRNAsSignal TransductionMicroRNAsCardioimmunologyCardiovascular diseaseHeartImmunologyMicroRNATREGS

Identifiers

PMID33483751
PMCPMC8562329
OpenAlexW3124026629

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.