Evidence map›Paper›PMID 40831172›Full record

ArticleZhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics2025

[Interferon-λ1 improves glucocorticoid resistance caused by respiratory syncytial virus by regulating the p38 mitogen-activated protein kinase signaling pathway].

Li Peng, Yao Liu, Fang-Cai Li, Xiao-Fang Ding, Xiao-Juan Lin, Tu-Hong Yang, Li-Li Zhong

Abstract readEnglish Abstract
In one paragraph

Article in Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Li PengChildren's Medical Center, Hunan Provincial People's Hospital/First Affiliated Hospital of Hunan Normal University/Hunan Key Laboratory of Pediatric Respiratory Diseases, Changsha 410005, China.
Yao LiuChildren's Medical Center, Hunan Provincial People's Hospital/First Affiliated Hospital of Hunan Normal University/Hunan Key Laboratory of Pediatric Respiratory Diseases, Changsha 410005, China.
Fang-Cai Li
Xiao-Fang DingChildren's Medical Center, Hunan Provincial People's Hospital/First Affiliated Hospital of Hunan Normal University/Hunan Key Laboratory of Pediatric Respiratory Diseases, Changsha 410005, China.
Xiao-Juan LinChildren's Medical Center, Hunan Provincial People's Hospital/First Affiliated Hospital of Hunan Normal University/Hunan Key Laboratory of Pediatric Respiratory Diseases, Changsha 410005, China.
Tu-Hong YangChildren's Medical Center, Hunan Provincial People's Hospital/First Affiliated Hospital of Hunan Normal University/Hunan Key Laboratory of Pediatric Respiratory Diseases, Changsha 410005, China.
Li-Li ZhongChildren's Medical Center, Hunan Provincial People's Hospital/First Affiliated Hospital of Hunan Normal University/Hunan Key Laboratory of Pediatric Respiratory Diseases, Changsha 410005, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo investigate the effect of interferon-λ1 (IFN-λ1) on glucocorticoid (GC) resistance in human bronchial epithelial cells (HBECs) stimulated by respiratory syncytial virus (RSV).

methodsHBECs were divided into five groups: control, dexamethasone, IFN-λ1, RSV, and RSV+IFN-λ1. CCK-8 assay was used to measure the effect of different concentrations of IFN-λ1 on the viability of HBECs, and the sensitivity of HBECs to dexamethasone was measured in each group. Quantitative real-time PCR was used to measure the mRNA expression levels of p38 mitogen-activated protein kinase (p38 MAPK), glucocorticoid receptor (GR), and MAPK phosphatase-1 (MKP-1). Western blot was used to measure the protein expression level of GR in cell nucleus and cytoplasm, and the nuclear/cytoplasmic ratio of GR was calculated.

resultsAt 24 and 72 hours, the proliferation activity of HBECs increased with the increase in IFN-λ1 concentration in a dose- and time-dependent manner (

conclusionsIFN-λ1 can inhibit the p38 MAPK pathway by upregulating MKP-1, promote the nuclear translocation of GR, and thus ameliorate GC resistance in HBECs.

Indexed as

DexamethasoneDrug ResistanceGlucocorticoidsMAP Kinase Signaling Systemp38 Mitogen-Activated Protein KinasesRespiratory Syncytial VirusesCells, CulturedDual Specificity Phosphatase 1Epithelial CellsHumansInterferonsReceptors, GlucocorticoidSignal TransductionDexamethasoneDual Specificity Phosphatase 1DUSP1 protein, humanGlucocorticoidsInterferonsp38 Mitogen-Activated Protein KinasesReceptors, GlucocorticoidGlucocorticoid resistanceHuman bronchial epithelial cellInterferon-λ1p38 mitogen-activated protein kinaseRespiratory syncytial virus

Identifiers

PMID40831172
PMCPMC12369537

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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.