Viroclinics Biosciences BV, Rotterdam 3029 AK, The Netherlands.
Department of Viroscience, Erasmus MC, Rotterdam 3015 CN, The Netherlands.
Viruses. 2018 Jan 2;10(1):18. doi: 10.3390/v10010018.
Human respiratory syncytial virus (HRSV) causes substantial morbidity and mortality in vulnerable patients, such as the very young, the elderly, and immunocompromised individuals of any age. Nosocomial transmission of HRSV remains a serious challenge in hospital settings, with intervention strategies largely limited to infection control measures, including isolation of cases, high standards of hand hygiene, cohort nursing, and use of personal protective equipment. No vaccines against HRSV are currently available, and treatment options are largely supportive care and expensive monoclonal antibody or antiviral therapy. The limitations of current animal models for HRSV infection impede the development of new preventive and therapeutic agents, and the assessment of their potential for limiting HRSV transmission, in particular in nosocomial settings. Here, we demonstrate the efficient transmission of HRSV from immunocompromised ferrets to both immunocompromised and immunocompetent contact ferrets, with pathological findings reproducing HRSV pathology in humans. The immunocompromised ferret-HRSV model represents a novel tool for the evaluation of intervention strategies against nosocomial transmission of HRSV.
人类呼吸道合胞病毒(HRSV)可导致易感染患者(如婴幼儿、老年人和任何年龄段的免疫功能低下者)出现严重疾病和死亡。医院环境中 HRSV 的医院内传播仍然是一个严重挑战,干预策略主要限于感染控制措施,包括病例隔离、高标准的手部卫生、分组护理和使用个人防护设备。目前尚无针对 HRSV 的疫苗,治疗方法主要是支持性护理以及昂贵的单克隆抗体或抗病毒治疗。目前用于 HRSV 感染的动物模型存在局限性,这阻碍了新的预防和治疗药物的开发,以及评估它们在限制 HRSV 传播(特别是在医院环境中)方面的潜力。在这里,我们证明了免疫功能低下的雪貂可有效地将 HRSV 传播给免疫功能低下和免疫功能正常的接触雪貂,其病理发现可重现人类的 HRSV 病理。免疫功能低下的雪貂-HRSV 模型代表了一种评估针对 HRSV 医院内传播的干预策略的新工具。