登革热病毒
生物
鉴定(生物学)
自身免疫
登革热
基孔肯雅
间接证据
转化研究
透视图(图形)
三域系统
病毒
免疫学
计算生物学
医学
病毒病机
大流行
病毒学
病毒系统动力学
生物信息学
疾病
神经科学
作者
Lin Yu,DuJiang Yang,Zhijun Ye,GuoYou Wang
摘要
ABSTRACT The recent review by Zhang et al. provides a valuable consolidation of clinical evidence linking Dengue virus (DENV), Chikungunya virus (CHIKV), and SARS‐CoV‐2 to bone‐related diseases. While their work aptly highlights this emerging clinical paradigm, our letter offers a critical analysis to propel the field from descriptive association to mechanistic causation. We identify and dissect several substantive gaps in the current narrative. Firstly, we challenge the prevailing yet often circumstantial evidence for direct viral infection of bone cells, arguing for the need to distinguish between productive infection and passive viral presence. Secondly, we call for a more nuanced deconstruction of the “cytokine storm” hypothesis, urging the identification of master regulators and a clearer delineation between viral persistence and virally‐induced autoimmunity in driving chronic pathology, such as post‐CHIKV arthritis. Furthermore, we emphasise the critical need for longitudinal studies to define the long‐term trajectory of bone health post‐SARS‐CoV‐2 infection, distinguishing transient from permanent metabolic defects. Finally, we propose a unified, comparative research framework utilising advanced models to uncover fundamental principles of virus‐bone interactions. This critical perspective underscores the necessity of a deeper, mechanism‐driven investigative agenda to inform future therapeutic strategies.
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