Evidence map›Paper›PMID 25980029›Full record

ReviewJournal of immunology (Baltimore, Md. : 1950)2015

Prospects for Therapeutic Targeting of MicroRNAs in Human Immunological Diseases.

Marisa E Luck, Stefan A Muljo, Colm B Collins

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of immunology (Baltimore, Md. : 1950), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.7field-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

23 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Epigenetics in osteoarthritis: Novel spotlight.Journal of cellular physiology · 2019
    Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. MicroRNAs and immunity in periodontal health and disease.International journal of oral science · 2018
    Review
  13. Article
  14. Editorial focus: entering into the non-coding RNA era.Cellular & molecular biology letters · 2018
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Mitochondrial Epigenetics and Environmental Exposure.Current environmental health reports · 2016
    Review
  20. Article
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 2 institutions in 1 country.

Marisa E LuckMucosal Inflammation Program, Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO 80045; and.
Stefan A MuljoIntegrative Immunobiology Unit, Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892 Stefan.Muljo@nih.gov Colm.Collins@ucdenver.edu.
Colm B CollinsMucosal Inflammation Program, Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO 80045; and Stefan.Muljo@nih.gov Colm.Collins@ucdenver.edu.
University of Colorado Denver · USNational Institute of Allergy and Infectious Diseases · US

Funding

Roles of non-Coding RNAs in Programming Lymphocyte Differentiation and FunctionZIAAI001131 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MULJO, STEFAN · 2010 to 2025
$11.0M
Selective MicoRNA modification to enhance regulatory T cell function in IBDK01DK099403 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI COLLINS, COLM · 2013 to 2017
$678k
Intramural NIH HHS ZIA AI001131NIDDK NIH HHS K01 DK099403NIDDK NIH HHS K01 DK099403-01
6 · The paper itself

Abstract

MicroRNAs (miRNAs) are endogenous oligoribonucleotides with exciting therapeutic potential. Early studies established a clear role for miRNAs in leukocyte biology. The first miRNA-based therapy, miravirsen, is now in phase 2 clinical trials, making the reality of these therapies undeniable. The capacity for miRNAs to fine-tune inflammatory signaling make them attractive treatment targets for immunological diseases. Nonetheless, the degree of redundancy among miRNAs, coupled with the promiscuity of miRNA binding sites in the transcriptome, require consideration when designing miRNA-directed interventions. Altered miRNA expression occurs across a range of inflammatory conditions, including inflammatory bowel disease, arthritis, and diabetes. However, very few studies successfully treated murine models of immunological diseases with miRNA-based approaches. While discussing recent studies targeting miRNAs to treat immunological conditions, we also reflect on the risks of miRNA targeting and showcase some newer delivery systems that may improve the pharmacological profile of this class of therapeutics.

Indexed as

Molecular Targeted TherapyAnimalsBinding SitesDrug Delivery SystemsHumansImmune System DiseasesInflammationMiceMicroRNAsOligonucleotidesMicroRNAsmiravirsenOligonucleotides

Identifiers

PMID25980029
PMCPMC4435821
OpenAlexW1504418083

What OpenQuestion holds

Textmetadata
LicenceTDM
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.