地塞米松和沙利单抗治疗新冠肺炎后单纯疱疹病毒-1再激活继发多器官功能障碍

Pub Date : 2023-04-01 DOI:10.2478/jccm-2023-0010
Thomas Roe, Sam Waddy, Nikitas Nikitas
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引用次数: 0

摘要

对SARS-CoV-2病毒的免疫应答和COVID-19疾病的治疗表现出对病毒再激活的潜在易感性,特别是单纯疱疹病毒1 (HSV-1)。病例介绍:一名49岁女性因严重COVID-19肺炎入院,给予沙利单抗和地塞米松治疗。她在重症监护病房(ICU)插管和通气,初步显示生化和临床证据的改善。随后出现呼吸、肾脏和心血管功能严重急性恶化,并伴有面部水疱疹。聚合酶链反应证实HSV-1再激活,并开始用阿昔洛韦治疗。在ICU住院49天后,患者成功脱离了所有器官支持,并取得了令人满意的恢复。结论:HSV-1再激活在COVID-19中很常见,可能导致较差的临床结果。引起病毒再激活易感性的机制尚不明确,然而,通过干扰素和白细胞介素途径的功能障碍导致危重疾病诱导的免疫抑制的发展可能是一种机制。这种效应可能会持续使用免疫抑制药物,尽管需要进一步的研究来描述这种现象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Multiple Organ Dysfunction Secondary to Herpes Simplex Virus -1 Reactivation After Treatment With Dexamethasone and Sarilumab for Covid-19 Disease.

Introduction: The immunological response to the SARS-CoV-2 virus and the treatment of COVID-19 disease present a potential susceptibility to viral reactivation, particularly Herpes simplex virus-1 (HSV-1).

Case presentation: A 49-year-old female presented to hospital with severe COVID-19 pneumonitis and was given sarilumab and dexamethasone. She was intubated and ventilated in the intensive care unit (ICU) and initially demonstrated biochemical and clinical evidence of improvement. This was followed by a severe acute deterioration in respiratory, renal, and cardiovascular function, accompanied by a vesicular rash on the face. Polymerase chain reaction confirmed HSV-1 reactivation and treatment with acyclovir was commenced. After 49 days in ICU the patient was successfully weaned from all organ support, and she made a satisfactory recovery.

Conclusions: HSV-1 reactivation is common in COVID-19 and likely contributes to poorer clinical outcomes. The mechanism causing susceptibility to viral reactivation is not clearly defined, however, the development of critical illness induced immunosuppression via dysfunction of interferon and interleukin pathways is a likely mechanism. This effect could be perpetuated with immunosuppressant medications, although further research is needed to characterise this phenomenon.

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