Wang Li-Chiu, Tsai Huey-Pin, Chen Shun-Hua, Wang Shih-Min
School of Medicine, I-Shou University, Kaohsiung, Taiwan.
Department of Pathology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Front Pharmacol. 2022 Oct 20;13:1014823. doi: 10.3389/fphar.2022.1014823. eCollection 2022.
Neonatal infection with nonpolio enteroviruses (EVs) causes nonspecific febrile illnesses and even life-threatening multiorgan failure. Hepatitis, which often results in hepatic necrosis followed by disseminated intravascular coagulopathy, is one of the most severe and frequent fatal neonatal EV infection complications. Coxsackievirus B (CVB) 1-5 and many echoviruses have been most commonly identified. Neonatal EV infection treatment has usually involved initial supportive care. Studies for CVB and echovirus infection treatments were developed for more than thirty years. Intravenous immunoglobulin and pleconaril therapy was performed in some clinical trials. Additionally, other studies demonstrated antiviral and/or anti-inflammatory pathogenesis mechanisms of neonatal EV hepatitis in or models. These treatments represented promising options for the clinical practice of neonatal EV hepatitis. However, further investigation is needed to elucidate the whole therapeutic potential and safety problems.
新生儿感染非脊髓灰质炎肠道病毒(EVs)会引发非特异性发热疾病,甚至危及生命的多器官功能衰竭。肝炎是最严重且常见的致命性新生儿EV感染并发症之一,常导致肝坏死,随后出现弥散性血管内凝血。最常检测到的是柯萨奇病毒B(CVB)1 - 5型以及多种埃可病毒。新生儿EV感染的治疗通常首先采取支持性护理。针对CVB和埃可病毒感染治疗的研究已开展了三十多年。一些临床试验采用了静脉注射免疫球蛋白和普来可那立疗法。此外,其他研究在体外或体内模型中证实了新生儿EV肝炎的抗病毒和/或抗炎发病机制。这些治疗方法为新生儿EV肝炎的临床实践提供了有前景的选择。然而,仍需进一步研究以阐明其整体治疗潜力和安全性问题。