Evidence map›Paper›PMID 42840130›Full record

ArticleFrontiers in public health2026

Shift work disrupts Immune regulation of the transcriptome in hospital nurses.

Huan-Yan Hu, Xiang-Feng Xu, Ze Yu, Li Fang, Ke-Xin Fang

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Article in Frontiers in public health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Huan-Yan HuDepartment of Rheumatology, Zhoushan Hospital, Wenzhou Medical University, Zhoushan, Zhejiang, China.
Xiang-Feng XuDepartment of Rheumatology, Zhoushan Hospital, Wenzhou Medical University, Zhoushan, Zhejiang, China.
Ze YuLaboratory of Cytobiology and Molecular Biology, Zhoushan Hospital, Wenzhou Medical University, Zhoushan, Zhejiang, China.
Li FangDepartment of Rheumatology, Zhoushan Hospital, Wenzhou Medical University, Zhoushan, Zhejiang, China.
Ke-Xin FangLaboratory of Cytobiology and Molecular Biology, Zhoushan Hospital, Wenzhou Medical University, Zhoushan, Zhejiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Shift work, especially night shifts in medicine, disrupts nurses' circadian rhythms, potentially causing immune dysregulation and health risks, with significant economic and medical burdens. The molecular mechanisms of shift work-related immune disorders are understudied. This research analyzes transcriptomes of nurses' peripheral blood mononuclear cells (PBMCs) from different shifts to identify key differentially expressed genes and explore their roles in immune regulation. Method: This study combined bioinformatics and animal experiments, analyzing the GSE122541 dataset for DEGs in day and night shift nurses' PBMCs. WGCNA identified core gene modules linked to night shift. Protein interaction networks were analyzed for hub genes, with expression validated in a circadian rhythm disorder mouse model. Results: The analysis found many differentially expressed genes in night shift nurses' PBMCs, mainly in immune pathways like T-cell receptor signaling and differentiation. WGCNA identified gene modules linked to night shifts, intersecting to reveal 8 candidate hub genes, with TRIM22 and JAK1 core in the network and downregulated in nurses. Mouse models showed Trim22 and Jak1 also decreased during nighttime activity, indicating their downregulation is a common trait in circadian rhythm disorders, involving interferon-γ and NF-κB immune signaling. Conclusion: This study shows that night shift work disrupts circadian rhythm and downregulates immune genes like

Indexed as

Leukocytes, MononuclearShift Work ScheduleTranscriptomeAnimalsCircadian RhythmComputational BiologyGene Expression ProfilingHumansMicecircadian rhythm disruptionimmune dysregulationjak1shift workTRIM22

Identifiers

PMID42840130
PMCPMC13638527

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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.