Evidence map›Paper›PMID 34223639›Full record

ArticleEuropean journal of immunology2021

Abortive HIV-1 RNA induces pro-IL-1β maturation via protein kinase PKR and inflammasome activation in humans.

Melissa Stunnenberg, John L van Hamme, Marjolein Trimp, Sonja I Gringhuis, Teunis B H Geijtenbeek

Open access · hybridAbstract read
In one paragraph

Article in European journal of immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Targeting inflammasomes as a therapeutic potential for HIV/AIDS.Cellular and molecular life sciences : CMLS · 2025
    Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Regulation and functions of the NLRP3 inflammasome in RNA virus infection.Frontiers in cellular and infection microbiology · 2023
    Review
  10. Review
  11. Article
  12. NLRP3-Mediated Inflammation in Atherosclerosis and Associated Therapeutics.Frontiers in cell and developmental biology · 2022
    Review
  13. 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

5 authors at 3 institutions in 2 countries.

Melissa StunnenbergAmsterdam UMC, Department of Experimental Immunology, University of Amsterdam, Amsterdam Institute for Infection & Immunity, Amsterdam, The Netherlands.
John L van HammeAmsterdam UMC, Department of Experimental Immunology, University of Amsterdam, Amsterdam Institute for Infection & Immunity, Amsterdam, The Netherlands.
Marjolein TrimpAmsterdam UMC, Department of Experimental Immunology, University of Amsterdam, Amsterdam Institute for Infection & Immunity, Amsterdam, The Netherlands.
Sonja I GringhuisAmsterdam UMC, Department of Experimental Immunology, University of Amsterdam, Amsterdam Institute for Infection & Immunity, Amsterdam, The Netherlands.
Teunis B H GeijtenbeekAmsterdam UMC, Department of Experimental Immunology, University of Amsterdam, Amsterdam Institute for Infection & Immunity, Amsterdam, The Netherlands.
University of Amsterdam · NLAmsterdam University Medical Centers · NLInstitute of Infection and Immunity · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The proinflammatory cytokine IL-1β mediates high levels of immune activation observed during acute and chronic human immunodeficiency virus 1 (HIV-1) infection. Little is known about the mechanisms that drive IL-1β activation during HIV-1 infection. Here, we have identified a crucial role for abortive HIV-1 RNAs in inducing IL-1β in humans. Abortive HIV-1 RNAs were sensed by protein kinase RNA-activated (PKR), which triggered activation of the canonical NLRP3 inflammasome and caspase-1, leading to pro-IL-1β processing and secretion. PKR activated the inflammasome via ROS generation and MAP kinases ERK1/2, JNK, and p38. Inhibition of PKR during HIV-1 infection blocked IL-1β production. As abortive HIV-1 RNAs are produced during productive infection and latency, our data strongly suggest that targeting PKR signaling might attenuate immune activation during acute and chronic HIV-1 infection.

Indexed as

eIF-2 KinaseHIV-1HIV InfectionsHost-Pathogen InteractionsHumansInflammasomesInterleukin-1betaMAP Kinase Signaling SystemNLR Family, Pyrin Domain-Containing 3 ProteinReactive Oxygen SpeciesReceptors, Pattern RecognitionRNA, ViralSignal TransductionEIF2AK2 protein, humaneIF-2 KinaseIL1B protein, humanInflammasomesInterleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinReactive Oxygen SpeciesReceptors, Pattern RecognitionRNA, ViralAbortive HIV-1 RNAHuman immunodeficiency virus 1Inflammasome activationPattern recognition receptorProtein kinase RNA-activated

Identifiers

PMID34223639
PMCPMC8518791
OpenAlexW3178248205

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.