Evidence map›Paper›PMID 38005883›Full record

ArticleViruses2023

MiR-155 Negatively Regulates Anti-Viral Innate Responses among HIV-Infected Progressors.

Puja Pawar, Jyotsna Gokavi, Shilpa Wakhare, Rajani Bagul, Ujjwala Ghule, Ishrat Khan, Varada Ganu, Anupam Mukherjee, Ashwini Shete, Amrita Rao and 1 more

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. 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

11 authors at 1 institution in 1 country.

Puja PawarDivision of Immunology and Serology, ICMR-National AIDS Research Institute, Pune 411026, India.ORCID 0009-0002-9958-1193
Jyotsna GokaviDivision of Immunology and Serology, ICMR-National AIDS Research Institute, Pune 411026, India.ORCID 0000-0002-1528-5884
Shilpa WakhareDivision of Immunology and Serology, ICMR-National AIDS Research Institute, Pune 411026, India.
Rajani BagulDivision of Clinical Sciences, ICMR-National AIDS Research Institute, Pune 411026, India.
Ujjwala GhuleDivision of Clinical Sciences, ICMR-National AIDS Research Institute, Pune 411026, India.
Ishrat KhanDivision of Virology, ICMR-National AIDS Research Institute, Pune 411026, India.
Varada GanuDivision of Immunology and Serology, ICMR-National AIDS Research Institute, Pune 411026, India.
Anupam MukherjeeDivision of Virology, ICMR-National AIDS Research Institute, Pune 411026, India.ORCID 0000-0002-0612-2258
Ashwini SheteDivision of Immunology and Serology, ICMR-National AIDS Research Institute, Pune 411026, India.ORCID 0000-0003-0791-2128
Amrita RaoDivision of Clinical Sciences, ICMR-National AIDS Research Institute, Pune 411026, India.ORCID 0000-0003-2950-9938
Vandana SaxenaDivision of Immunology and Serology, ICMR-National AIDS Research Institute, Pune 411026, India.ORCID 0000-0002-7443-806X
National AIDS Research Institute · IN

Funding

Indian Council of Medical Research HIV/50/180/11/2015-ECD-II
6 · The paper itself

Abstract

HIV infection impairs host immunity, leading to progressive disease. An anti-retroviral treatment efficiently controls viremia but cannot completely restore the immune dysfunction in HIV-infected individuals. Both host and viral factors determine the rate of disease progression. Among the host factors, innate immunity plays a critical role; however, the mechanism(s) associated with dysfunctional innate responses are poorly understood among HIV disease progressors, which was investigated here. The gene expression profiles of TLRs and innate cytokines in HIV-infected (LTNPs and progressors) and HIV-uninfected individuals were examined. Since the progressors showed a dysregulated TLR-mediated innate response, we investigated the role of TLR agonists in restoring the innate functions of the progressors. The stimulation of PBMCs with TLR3 agonist-poly:(I:C), TLR7 agonist-GS-9620 and TLR9 agonist-ODN 2216 resulted in an increased expression of IFN-α, IFN-β and IL-6. Interestingly, the expression of

Indexed as

HIV InfectionsMicroRNAsAntiviral AgentsCytokinesDisease ProgressionHumansImmunity, InnateMembrane ProteinsRNA-Binding ProteinsToll-Like Receptor 3Toll-Like Receptor 7Antiviral AgentsCytokinesIFITM3 protein, humanMembrane ProteinsMicroRNAsMIRN155 microRNA, humanRNA-Binding ProteinsToll-Like Receptor 3Toll-Like Receptor 7disease progressionHIVhost restriction factorsinnateLTNPsmiR-155TLRs

Identifiers

PMID38005883
PMCPMC10675553
OpenAlexW4388141288

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.