Sheng-Che Lin , Chiou-Feng Lin , Szu-Yuan Wu , Chih-Chieh Yang , Wan-Ming Chen , Po-Chun Tseng , Fu-Chia Shih , Josephine Diony Nanda , Chia-Ling Chen
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引用次数: 0
Abstract
Background
Night shifts may disrupt circadian rhythms and immunity, potentially leading to health issues such as increased susceptibility to infectious diseases and impaired vaccine responses. This concern is particularly relevant for hospital employees during the COVID-19 pandemic. Our study aims to investigate the immune homeostasis of hospital workers engaged in rotating night shifts during the pandemic.
Methods
Healthy hospital employees aged 18–60 were enrolled and divided into two groups: the day shift (DS) group (n = 19) and the rotating night shift (RNS) group (n = 40). Blood samples were collected for analysis, including complete blood count, biochemistry, cytokines, anti-SARS-CoV-2 S1 antibody (anti-S1 IgG) titers, and immune cell subsets.
Results
The RNS group exhibited skewed Th1 immunity, characterized by significant elevations in IL-6 and IL-22, increasing trends in TNF-α and the IFN-γ/IL-5 ratio, along with a significant reduction in IL-5. Both groups demonstrated comparable rates of COVID-19 infection, and all participants showed effectively boosted anti-S1 IgG titers following antigen exposure (natural infection or vaccination). However, the RNS had lower anti-S1 IgG titers 3 to 6 months after antigen exposure. Additionally, decreased proportions of naïve B, and NKT cells along with an increase in T cell subsets, were detected in the RNS group. A significant positive correlation was also found between anti-S1 IgG titers and the proportion of NKT cells.
Conclusion
These findings suggest that RNS work induces low-grade inflammation and disrupts immune homeostasis, possibly lowering long-term anti-S1 IgG level after COVID-19 antigen exposure.
期刊介绍:
The journal Cytokine has an open access mirror journal Cytokine: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review.
* Devoted exclusively to the study of the molecular biology, genetics, biochemistry, immunology, genome-wide association studies, pathobiology, diagnostic and clinical applications of all known interleukins, hematopoietic factors, growth factors, cytotoxins, interferons, new cytokines, and chemokines, Cytokine provides comprehensive coverage of cytokines and their mechanisms of actions, 12 times a year by publishing original high quality refereed scientific papers from prominent investigators in both the academic and industrial sectors.
We will publish 3 major types of manuscripts:
1) Original manuscripts describing research results.
2) Basic and clinical reviews describing cytokine actions and regulation.
3) Short commentaries/perspectives on recently published aspects of cytokines, pathogenesis and clinical results.