| Literature DB >> 33658482 |
Yingying Lu1,2, Feng Liu3, Gangling Tong4, Feng Qiu3, Pinhong Song3, Xiaolin Wang5, Xiafei Zou5, Deyun Wan6, Miao Cui7, Yunsheng Xu8, Zhihua Zheng2, Peng Hong9,10,11.
Abstract
Synthetic glucocorticoid dexamethasone is the first trial-proven drug that reduces COVID-19 mortality by suppressing immune system. In contrast, interferons are a crucial component of host antiviral immunity and can be directly suppressed by glucocorticoids. To investigate whether therapeutic interferons can compensate glucocorticoids-induced loss of antiviral immunity, we retrospectively analyzed a cohort of 387 PCR-confirmed COVID-19 patients with quasi-random exposure to interferons and conditional exposure to glucocorticoids. Among patients receiving glucocorticoids, early interferon therapy was associated with earlier hospital discharge (adjusted HR 1.68, 95% CI 1.19-2.37) and symptom relief (adjusted HR 1.48, 95% CI 1.06-2.08), while these associations were insignificant among glucocorticoids nonusers. Early interferon therapy was also associated with lower prevalence of prolonged viral shedding (adjusted OR 0.24, 95% CI 0.10-0.57) only among glucocorticoids users. Additionally, these associations were glucocorticoid cumulative dose- and timing-dependent. These findings reveal potential therapeutic synergy between interferons and glucocorticoids in COVID-19 that warrants further investigation.Entities:
Year: 2021 PMID: 33658482 PMCID: PMC7925812 DOI: 10.1038/s41392-021-00496-5
Source DB: PubMed Journal: Signal Transduct Target Ther ISSN: 2059-3635