Evidence map›Paper›PMID 33086748›Full record

ArticleInternational journal of molecular sciences2020

Interferon-Mediated Long Non-Coding RNA Response in Macrophages in the Context of HIV.

Tinus Schynkel, Matthew A Szaniawski, Adam M Spivak, Alberto Bosque, Vicente Planelles, Linos Vandekerckhove, Wim Trypsteen

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. 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 31% 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, 13 citations in OpenAlex.

  1. Review
  2. Evaluating lncRNA Expression Patterns during HIV-1 Treatment Interruption.International journal of molecular sciences · 2023
    Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Heliyon · 2021
    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

7 authors at 3 institutions in 2 countries.

Tinus SchynkelHIV Cure Research Center, Department of Internal Medicine and Pediatrics, Ghent University and Ghent University Hospital, 9000 Ghent, Belgium.ORCID 0000-0001-5936-0906
Matthew A SzaniawskiDivision of Microbiology and Immunology, Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT 84132, USA.ORCID 0000-0003-1123-3101
Adam M SpivakDivision of Infectious Diseases, Department of Medicine, University of Utah School of Medicine, Salt Lake City, UT 84132, USA.
Alberto BosqueDepartment of Microbiology, Immunology and Tropical Medicine, School of Medicine & Health Sciences, George Washington University, Washington, DC 20037, USA.
Vicente PlanellesDivision of Microbiology and Immunology, Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT 84132, USA.
Linos VandekerckhoveHIV Cure Research Center, Department of Internal Medicine and Pediatrics, Ghent University and Ghent University Hospital, 9000 Ghent, Belgium.
Wim TrypsteenHIV Cure Research Center, Department of Internal Medicine and Pediatrics, Ghent University and Ghent University Hospital, 9000 Ghent, Belgium.ORCID 0000-0001-9066-4932
Ghent University Hospital · BEUniversity of Utah · USGeorge Washington University · US

Funding

Fonds Wetenschappelijk Onderzoek 1.8.020.09.N.00Fonds Wetenschappelijk Onderzoek 1S41219NNIH HHS AI143567-01
6 · The paper itself

Abstract

Interferons play a critical role in the innate immune response against a variety of pathogens, such as HIV-1. Recent studies have shown that long non-coding genes are part of a reciprocal feedforward/feedback relationship with interferon expression. They presumably contribute to the cell type specificity of the interferon response, such as the phenotypic and functional transition of macrophages throughout the immune response. However, no comprehensive understanding exists today about the IFN-lncRNA interplay in macrophages, also a sanctuary for latent HIV-1. Therefore, we completed a poly-A+ RNAseq analysis on monocyte-derived macrophages (MDMs) treated with members of all three types of IFNs (IFN-α, IFN-ε, IFN-γ or IFN-λ) and on macrophages infected with HIV-1, revealing an extensive non-coding IFN and/or HIV-1 response. Moreover, co-expression correlation with mRNAs was used to identify important (long) non-coding hub genes within IFN- or HIV-1-associated gene clusters. This study identified and prioritized IFN related hub lncRNAs for further functional validation.

Indexed as

Gene Expression RegulationGene OntologyGene Regulatory NetworksHIV-1HIV InfectionsHumansInterferonsMacrophagesRNA, Long NoncodingRNA, MessengerTranscriptomeInterferonsRNA, Long NoncodingRNA, MessengerHuman Immunodeficiency Virus (HIV)interferonlong non-coding RNAmacrophageRNA-seq

Identifiers

PMID33086748
PMCPMC7589721
OpenAlexW3092900783

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.