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强效中和的人源单克隆抗体可预防裂谷热脑炎。

Potent neutralizing human monoclonal antibodies protect from Rift Valley fever encephalitis.

机构信息

Department of Infectious Diseases and Microbiology, School of Public Health, and.

Center for Vaccine Research, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

出版信息

JCI Insight. 2024 Aug 1;9(18):e180151. doi: 10.1172/jci.insight.180151.

Abstract

Rift Valley fever (RVF) is an emerging arboviral disease affecting both humans and livestock. In humans, RVF displays a spectrum of clinical manifestations, including encephalitis. To date, there are no FDA-approved vaccines or therapeutics for human use, although several are in preclinical development. Few small-animal models of RVF encephalitis exist, further complicating countermeasure assessment. Human mAbs RVFV-140, RVFV-268, and RVFV-379 are recombinant potently neutralizing antibodies that prevent infection by binding the RVFV surface glycoproteins. Previous studies showed that both RVFV-268 and RVFV-140 improve survival in a lethal mouse model of disease, and RVFV-268 has prevented vertical transmission in a pregnant rat model of infection. Despite these successes, evaluation of mAbs in the context of brain disease has been limited. This is the first study to our knowledge to assess neutralizing antibodies for prevention of RVF neurologic disease using a rat model. Administration of RVFV-140, RVFV-268, or RVFV-379 24 hours prior to aerosol exposure to the virulent ZH501 strain of RVFV resulted in substantially enhanced survival and lack of neurological signs of disease. These results using a stringent and highly lethal aerosol infection model support the potential use of human mAbs to prevent the development of RVF encephalitis.

摘要

裂谷热(RVF)是一种新兴的虫媒病毒性疾病,影响人类和牲畜。在人类中,RVF 表现出一系列临床表现,包括脑炎。迄今为止,尚无 FDA 批准的人类使用的疫苗或疗法,尽管有几种正在临床前开发中。RVF 脑炎的小动物模型很少,进一步增加了对策评估的复杂性。人源单克隆抗体 RVFV-140、RVFV-268 和 RVFV-379 是重组的强效中和抗体,通过与 RVFV 表面糖蛋白结合来预防感染。先前的研究表明,RVFV-268 和 RVFV-140 均可提高疾病致死性小鼠模型的存活率,并且 RVFV-268 已防止了感染的孕鼠模型中的垂直传播。尽管取得了这些成功,但在脑部疾病背景下对 mAb 的评估仍然有限。这是我们所知的首次使用大鼠模型评估预防 RVF 神经疾病的中和抗体的研究。在气溶胶暴露于强毒 RVFV-ZH501 株之前 24 小时给予 RVFV-140、RVFV-268 或 RVFV-379,可显著提高存活率并缺乏疾病的神经症状。这些使用严格和高度致死性气溶胶感染模型的结果支持使用人源 mAb 预防 RVF 脑炎的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70fb/11457859/748ac4cbe218/jciinsight-9-180151-g171.jpg

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