Evidence map›Paper›PMID 36503686›Full record

ReviewTrends in immunology2023

New insights into transcription elongation control of HIV-1 latency and rebound.

Uri Mbonye, Fredrick Kizito, Jonathan Karn

Abstract readReview
In one paragraph

Review in Trends in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

18 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
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  11. Review
  12. Structural rearrangements in the nucleus localize latent HIV proviruses to a perinucleolar compartment supportive of reactivation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  13. Article
  14. Review
  15. Article
  16. Decoding Heterogenous Single-cell Perturbation Responses.bioRxiv : the preprint server for biology · 2023
    Article
  17. Article
  18. 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 1 institution in 1 country.

Uri MbonyeDepartment of Molecular Biology and Microbiology, Case Western Reserve University, Cleveland, OH, USA.
Fredrick KizitoDepartment of Molecular Biology and Microbiology, Case Western Reserve University, Cleveland, OH, USA.
Jonathan KarnDepartment of Molecular Biology and Microbiology, Case Western Reserve University, Cleveland, OH, USA. Electronic address: jxk153@case.edu.
Case Western Reserve University · US

Funding

WG3: HIV, Co-infections and Co-morbiditiesP30AI036219 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI Immaculate Lillian Nankya · 1994 to 2026
$50.0M
Identification and eliminationof HIV reservoirs in oral lymphoid tissues by engineered NK cells.R01DE025464 · NIDCR · CASE WESTERN RESERVE UNIVERSITY · PI KARN, JONATHAN · 2015 to 2019
$3.8M
Microbiology and Immunology Training for HIV and HIV-Related Research in Uganda (MITHU)D43TW010319 · FIC · CASE WESTERN RESERVE UNIVERSITY · PI BOOM, W. HENRY, JOLOBA, MOSES LUTAAKOME · 2016 to 2025
$3.1M
The role of RNA m6A modification in the regulation of HIV latency and reactivationR61AI169629 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI KARN, JONATHAN · 2022 to 2024
$2.1M
Control of P-TEFb biogenesis and HIV transcription in primary T-cellsR01AI148083 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI KARN, JONATHAN, MBONYE, URI · 2019 to 2023
$2.0M
Molecular mechanisms regulating HIV entry and exit from latencyR01AI067093 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI KARN, JONATHAN · 2007 to 2011
$1.9M
FIC NIH HHS D43 TW010319NIAID NIH HHS P30 AI036219NIAID NIH HHS R01 AI067093NIAID NIH HHS R01 AI148083NIAID NIH HHS R61 AI169629NIDCR NIH HHS R01 DE025464
6 · The paper itself

Abstract

Antiretroviral therapy reduces circulating HIV-1 to undetectable amounts but does not eliminate the virus due to the persistence of a stable reservoir of latently infected cells. The reservoir is maintained both by proliferation of latently infected cells and by reseeding from reactivated cells. A major challenge for the field is to find safe and effective methods to eliminate this source of rebounding HIV-1. Studies on the molecular mechanisms leading to HIV-1 latency and reactivation are being transformed using latency models in primary and patient CD4

Indexed as

HIV-1HIV InfectionsCD4-Positive T-LymphocytesHumansPositive Transcriptional Elongation Factor BTranscription, GeneticVirus LatencyPositive Transcriptional Elongation Factor B7SK snRNPHIV-1 latencyHIV-1 reservoirHIV-1 Tatlatency reversalP-TEFbT cell receptor signaling

Identifiers

PMID36503686
PMCPMC11932764
OpenAlexW4311090314

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.