Evidence map›Paper›PMID 38249297›Full record

ReviewFrontiers in cellular and infection microbiology2023

Regulation and functions of the NLRP3 inflammasome in RNA virus infection.

Zhaoyang Yue, Xuelong Zhang, Yu Gu, Ying Liu, Lin-Miaoshen Lan, Yilin Liu, Yongkui Li, Ge Yang, Pin Wan, Xin Chen

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cellular and infection microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
5.8field-weighted citation impact, top 3% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. iPSC-derived human cortical organoids display profound alterations of cellular homeostasis following SARS-CoV-2 infection and Spike protein exposure.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. 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

10 authors at 2 institutions in 1 country.

Zhaoyang Yue *Institute of Medical Microbiology, College of Life Science and Technology, Jinan University, Guangzhou, China.
Xuelong Zhang *Institute of Medical Microbiology, College of Life Science and Technology, Jinan University, Guangzhou, China.
Yu GuInstitute of Medical Microbiology, College of Life Science and Technology, Jinan University, Guangzhou, China.
Ying LiuInstitute of Medical Microbiology, College of Life Science and Technology, Jinan University, Guangzhou, China.
Lin-Miaoshen LanInstitute of Medical Microbiology, College of Life Science and Technology, Jinan University, Guangzhou, China.
Yilin LiuInstitute of Medical Microbiology, College of Life Science and Technology, Jinan University, Guangzhou, China.
Yongkui LiInstitute of Medical Microbiology, College of Life Science and Technology, Jinan University, Guangzhou, China.
Ge YangFoshan Institute of Medical Microbiology, Foshan, China.
Pin WanFoshan Institute of Medical Microbiology, Foshan, China.
Xin ChenInstitute of Medical Microbiology, College of Life Science and Technology, Jinan University, Guangzhou, China.
Jinan University · CNJianghan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Virus infection is one of the greatest threats to human life and health. In response to viral infection, the host's innate immune system triggers an antiviral immune response mostly mediated by inflammatory processes. Among the many pathways involved, the nucleotide-binding oligomerization domain (NOD)-like receptor protein 3 (NLRP3) inflammasome has received wide attention in the context of viral infection. The NLRP3 inflammasome is an intracellular sensor composed of three components, including the innate immune receptor NLRP3, adaptor apoptosis-associated speck-like protein containing CARD (ASC), and the cysteine protease caspase-1. After being assembled, the NLRP3 inflammasome can trigger caspase-1 to induce gasdermin D (GSDMD)-dependent pyroptosis, promoting the maturation and secretion of proinflammatory cytokines such as interleukin-1 (IL-1β) and interleukin-18 (IL-18). Recent studies have revealed that a variety of viruses activate or inhibit the NLRP3 inflammasome via viral particles, proteins, and nucleic acids. In this review, we present a variety of regulatory mechanisms and functions of the NLRP3 inflammasome upon RNA viral infection and demonstrate multiple therapeutic strategies that target the NLRP3 inflammasome for anti-inflammatory effects in viral infection.

Indexed as

InflammasomesRNA Virus InfectionsCaspase 1HumansInterleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinCaspase 1InflammasomesInterleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteininflammationNLRP3 inflammasomepyroptosisRNA virustherapeutic strategy

Identifiers

PMID38249297
PMCPMC10796458
OpenAlexW4390610922

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.