Evidence map›Paper›PMID 31562757›Full record

ArticleThe Journal of infectious diseases2020

Activation of C-Type Lectin Receptor and (RIG)-I-Like Receptors Contributes to Proinflammatory Response in Middle East Respiratory Syndrome Coronavirus-Infected Macrophages.

Xiaoyu Zhao, Hin Chu, Bosco Ho-Yin Wong, Man Chun Chiu, Dong Wang, Cun Li, Xiaojuan Liu, Dong Yang, Vincent Kwok-Man Poon, Jianpiao Cai and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

40 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
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  6. Human coronaviruses: activation and antagonism of innate immune responses.Microbiology and molecular biology reviews : MMBR · 2025
    Review
  7. Anti-interferon armamentarium of human coronaviruses.Cellular and molecular life sciences : CMLS · 2025
    Review
  8. Article
  9. Article
  10. Article
  11. Innate immune recognition against SARS-CoV-2.Inflammation and regeneration · 2023
    Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. A mechanism of self-lipid endocytosis mediated by the receptor Mincle.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  18. Article
  19. Article
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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

14 authors at 1 institution in 1 country.

Xiaoyu ZhaoState Key Laboratory of Emerging Infectious Diseases, Pokfulam, Hong Kong.
Hin ChuState Key Laboratory of Emerging Infectious Diseases, Pokfulam, Hong Kong.
Bosco Ho-Yin WongState Key Laboratory of Emerging Infectious Diseases, Pokfulam, Hong Kong.
Man Chun ChiuDepartment of Microbiology, Pokfulam, Hong Kong.
Dong WangDepartment of Microbiology, Pokfulam, Hong Kong.
Cun LiDepartment of Microbiology, Pokfulam, Hong Kong.
Xiaojuan LiuDepartment of Microbiology, Pokfulam, Hong Kong.
Dong YangDepartment of Microbiology, Pokfulam, Hong Kong.
Vincent Kwok-Man PoonDepartment of Microbiology, Pokfulam, Hong Kong.
Jianpiao CaiDepartment of Microbiology, Pokfulam, Hong Kong.
Jasper Fuk-Woo ChanState Key Laboratory of Emerging Infectious Diseases, Pokfulam, Hong Kong.
Kelvin Kai-Wang ToState Key Laboratory of Emerging Infectious Diseases, Pokfulam, Hong Kong.
Jie ZhouState Key Laboratory of Emerging Infectious Diseases, Pokfulam, Hong Kong.
Kwok-Yung YuenState Key Laboratory of Emerging Infectious Diseases, Pokfulam, Hong Kong.
University of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman infection with Middle East respiratory syndrome coronavirus (MERS-CoV) poses an ongoing threat to public health worldwide. The studies of MERS patients with severe disease and experimentally infected animals showed that robust viral replication and intensive proinflammatory response in lung tissues contribute to high pathogenicity of MERS-CoV. We sought to identify pattern recognition receptor (PRR) signaling pathway(s) that mediates the inflammatory cascade in human macrophages upon MERS-CoV infection.

methodsThe potential signaling pathways were manipulated individually by pharmacological inhibition, small interfering ribonucleic acid (siRNA) depletion, and antibody blocking. The MERS-CoV-induced proinflammatory response was evaluated by measuring the expression levels of key cytokines and/or chemokines. Reverse transcription-quantitative polymerase chain reaction assay, flow cytometry analysis, and Western blotting were applied to evaluate the activation of related PRRs and engagement of adaptors.

resultsMERS-CoV replication significantly upregulated C-type lectin receptor (CLR) macrophage-inducible Ca2+-dependent lectin receptor (Mincle). The role of Mincle for MERS-CoV-triggered cytokine/chemokine induction was established based on the results of antibody blockage, siRNA depletion of Mincle and its adaptor spleen tyrosine kinase (Syk), and Syk pharmacological inhibition. The cytokine and/or chemokine induction was significantly attenuated by siRNA depletion of retinoic acid-inducible-I-like receptors (RLR) or adaptor, indicating that RLR signaling also contributed to MERS-CoV-induced proinflammatory response.

conclusionsThe CLR and RLR pathways are activated and contribute to the proinflammatory response in MERS-CoV-infected macrophages.

Indexed as

AnimalsCARD Signaling Adaptor ProteinsChemokinesChlorocebus aethiopsCoronavirus InfectionsCytokinesDEAD Box Protein 58Gene Knockdown TechniquesHumansLectins, C-TypeLungMacrophagesMiddle East Respiratory Syndrome CoronavirusReceptors, ImmunologicRNA, Small InterferingSignal TransductionCARD Signaling Adaptor ProteinsChemokinesCLEC4D protein, humanCytokinesDEAD Box Protein 58Lectins, C-TypeReceptors, ImmunologicRIGI protein, humanRNA, Small InterferingTretinoinCLRMERS-CoVMincleproinflammatory responseRLR

Identifiers

PMID31562757
PMCPMC7107474
OpenAlexW2976722941

What OpenQuestion holds

Textmetadata
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.