da Silva Felipe Paes Gomes, Matte Rafael, Wiedmer David Batista, da Silva Arthur Paes Gomes, Menin Rafaela Makiak, Barbosa Fernanda Bressianini, Meneguzzi Thainá Aymê Mocelin, Pereira Sabrina Barancelli, Fausto Amanda Terres, Klug Larissa, Melim Bruna Pinheiro, Beltrão Claudio Jose
School of Medicine and Life Sciences, Pontifícia Universidade Católica do Paraná-PUCPR, R. Imaculada Conceição, 1155-Prado Velho, Curitiba 80215-901, PR, Brazil.
School of Medicine, Faculdade Evangélica Mackenzie do Paraná, R. Padre Anchieta, no. 2770-Bigorrilho, Curitiba 80730-000, PR, Brazil.
Int J Mol Sci. 2025 Apr 28;26(9):4202. doi: 10.3390/ijms26094202.
The COVID-19 pandemic, driven by SARS-CoV-2, has led to a global health crisis, highlighting the virus's unique molecular mechanisms that distinguish it from other respiratory pathogens. It is known that the Hypoxia-Inducible Factor 1α (HIF-1α) activates a complex network of intracellular signaling pathways regulating cellular energy metabolism, angiogenesis, and cell survival, contributing to the wide range of clinical manifestations of COVID-19, including Post-Acute COVID-19 Syndrome (PACS). Emerging evidence suggests that dysregulation of HIF-1α is a key driver of systemic inflammation, silent hypoxia, and pathological tissue remodeling in both the acute and post-acute phases of the disease. This scoping review was conducted following PRISMA-ScR guidelines and registered in INPLASY. It involved a literature search in Scopus and PubMed, supplemented by manual reference screening, with study selection facilitated by Rayyan software. Our analysis clarifies the dual role of HIF-1α, which may either worsen inflammatory responses and viral persistence or support adaptive mechanisms that reduce cellular damage. The potential for targeting HIF-1α therapeutically in COVID-19 is complex, requiring further investigation to clarify its precise role and translational applications. This review deepens the molecular understanding of SARS-CoV-2-induced cellular and tissue dysfunction in hypoxia, offering insights for improving clinical management strategies and addressing long-term sequelae.
由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引发的2019冠状病毒病(COVID-19)大流行已导致全球卫生危机,凸显了该病毒与其他呼吸道病原体不同的独特分子机制。已知缺氧诱导因子1α(HIF-1α)激活一个复杂的细胞内信号通路网络,调节细胞能量代谢、血管生成和细胞存活,这导致了COVID-19的广泛临床表现,包括急性后COVID-19综合征(PACS)。新出现的证据表明,HIF-1α失调是该疾病急性和急性后期全身炎症、沉默性缺氧和病理性组织重塑的关键驱动因素。本综述性研究遵循PRISMA-ScR指南进行,并在INPLASY注册。它涉及在Scopus和PubMed中进行文献检索,并辅以手动参考文献筛选,由Rayyan软件协助进行研究选择。我们的分析阐明了HIF-1α的双重作用,它可能会加剧炎症反应和病毒持续存在,也可能支持减少细胞损伤的适应性机制。在COVID-19中针对HIF-1α进行治疗的潜力很复杂,需要进一步研究以阐明其确切作用和转化应用。本综述加深了对SARS-CoV-2在缺氧状态下诱导的细胞和组织功能障碍的分子理解,为改进临床管理策略和解决长期后遗症提供了见解。