Evidence map›Paper›PMID 33504607›Full record

ArticleJournal of virology2021

Respiratory syncytial virus activates Rab5a to suppress IRF1-dependent IFN-λ production, subverting the antiviral defense of airway epithelial cells.

Shi Mo, Wei Tang, Jun Xie, Sisi Chen, Luo Ren, Na Zang, Xiaohong Xie, Yu Deng, Leiqiong Gao, Enmei Liu

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Journal of virology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 26 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Shi MoDepartment of Respiratory Medicine, Children's Hospital of Chongqing Medical University, Chongqing, P.R. China.
Wei TangDepartment of Respiratory Medicine, Children's Hospital of Chongqing Medical University, Chongqing, P.R. China.
Jun XieDepartment of Respiratory Medicine, Children's Hospital of Chongqing Medical University, Chongqing, P.R. China.
Sisi ChenDepartment of Respiratory Medicine, Children's Hospital of Chongqing Medical University, Chongqing, P.R. China.
Luo RenDepartment of Respiratory Medicine, Children's Hospital of Chongqing Medical University, Chongqing, P.R. China.
Na ZangDepartment of Respiratory Medicine, Children's Hospital of Chongqing Medical University, Chongqing, P.R. China.
Xiaohong XieDepartment of Respiratory Medicine, Children's Hospital of Chongqing Medical University, Chongqing, P.R. China.
Yu DengDepartment of Respiratory Medicine, Children's Hospital of Chongqing Medical University, Chongqing, P.R. China.
Leiqiong GaoDepartment of Respiratory Medicine, Children's Hospital of Chongqing Medical University, Chongqing, P.R. China. 814983821@qq.com emliu186@126.com.
Enmei LiuDepartment of Respiratory Medicine, Children's Hospital of Chongqing Medical University, Chongqing, P.R. China. 814983821@qq.com emliu186@126.com.
Chongqing Medical University · CNChildren's Hospital of Chongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The limited antiviral options and lack of an effective vaccine against human respiratory syncytial virus (RSV) highlight the need for a novel antiviral therapy. One alternative is to identify and target the host factors required for viral infection. Here, using RNA interference to knock down Rab proteins, we provide multiple lines of evidence that Rab5a is required for RSV infection: (a) Rab5a is upregulated both in RSV-A2-infected A549 cells and RSV-A2-challenged BALB/c mice's airway epithelial cells at early infection phase; (b) shRNA-mediated knockdown of Rab5a is associated with reduced lung pathology in RSV A2 challenged mice; (c) Rab5a expression is correlated with disease severity of RSV infection of infants. Knockdown of Rab5a increases IFN-λ (lambda) production by mediating IRF1 nuclear translocation. Our results highlight a new role for Rab5a in RSV infection, such that its depletion inhibits RSV infection by stimulating the endogenous respiratory epithelial antiviral immunity, which suggests that Rab5a is a potential target for novel therapeutics against RSV infection.

Identifiers

PMID33504607
PMCPMC8103688
OpenAlexW3121707755

What OpenQuestion holds

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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.