Convalescent human plasma candidate reference materials protect against Crimean-Congo haemorrhagic fever virus (CCHFV) challenge in an A129 mouse model

IF 2.5 4区 医学 Q3 VIROLOGY Virus research Pub Date : 2024-06-01 DOI:10.1016/j.virusres.2024.199409
Sarah Kempster , Mark Hassall , Victoria Graham , Emma Kennedy , Stephen Findlay-Wilson , Francisco J. Salguero , Binnur Bagci , Nazif Elaldi , Murtaza Oz , Tuba Tasseten , Frank W. Charlton , John N. Barr , Juan Fontana , Chinwe Duru , Ernest Ezeajughi , Paul Matejtschuk , Ulrike Arnold , Yemisi Adedeji , Ali Mirazimi , Roger Hewson , Neil Almond
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Abstract

Crimean-Congo Haemorrhagic Fever Virus (CCHFV) is spread by infected ticks or direct contact with blood, tissues and fluids from infected patients or livestock. Infection with CCHFV causes severe haemorrhagic fever in humans which is fatal in up to 83 % of cases. CCHFV is listed as a priority pathogen by the World Health Organization (WHO) and there are currently no widely-approved vaccines. Defining a serological correlate of protection against CCHFV infection would support the development of vaccines by providing a ‘target threshold’ for pre-clinical and clinical immunogenicity studies to achieve in subjects and potentially obviate the need for in vivo protection studies. We therefore sought to establish titratable protection against CCHFV using pooled human convalescent plasma, in a mouse model. Convalescent plasma collected from seven individuals with a known previous CCHFV virus infection were characterised using binding antibody and neutralisation assays. All plasma recognised nucleoprotein and the Gc glycoprotein, but some had a lower Gn glycoprotein response by ELISA. Pooled plasma and two individual donations from convalescent donors were administered intraperitoneally to A129 mice 24 h prior to intradermal challenge with CCHFV (strain IbAr10200). A partial protective effect was observed with all three convalescent plasmas characterised by longer survival post-challenge and reduced clinical score. These protective responses were titratable. Further characterisation of the serological reactivities within these samples will establish their value as reference materials to support assay harmonisation and accelerate vaccine development for CCHFV.

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在 A129 小鼠模型中,康复人血浆候选参考材料可抵御克里米亚-刚果出血热病毒(CCHFV)的挑战。
克里米亚-刚果出血热病毒(CCHFV)通过受感染的蜱虫或直接接触受感染病人或牲畜的血液、组织和体液传播。感染 CCHFV 后,人类会出现严重的出血热,高达 83% 的病例会导致死亡。CCHFV 被世界卫生组织(WHO)列为重点病原体,目前还没有得到广泛认可的疫苗。确定CCHFV感染保护的血清学相关因素将为临床前和临床免疫原性研究提供一个 "目标阈值",从而支持疫苗的开发,并有可能避免进行体内保护研究。因此,我们试图在小鼠模型中使用汇集的人类康复血浆建立针对 CCHFV 的滴定保护。我们使用结合抗体和中和试验对从已知曾感染过 CCHFV 病毒的七个人身上采集的康复血浆进行了鉴定。所有血浆都能识别核蛋白和 Gc 糖蛋白,但有些血浆的 ELISA Gn 糖蛋白反应较低。在 A129 小鼠接受 CCHFV(IbAr10200 株)皮内挑战前 24 小时,给小鼠腹腔注射汇集的血浆和来自康复捐献者的两份单独捐献的血浆。这三种康复血浆都具有部分保护作用,其特点是挑战后存活时间更长,临床评分降低。这些保护性反应是可滴定的。对这些样本中血清反应性的进一步鉴定将确定它们作为参考材料的价值,以支持检测方法的统一和加速 CCHFV 疫苗的开发。
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来源期刊
Virus research
Virus research 医学-病毒学
CiteScore
9.50
自引率
2.00%
发文量
239
审稿时长
43 days
期刊介绍: Virus Research provides a means of fast publication for original papers on fundamental research in virology. Contributions on new developments concerning virus structure, replication, pathogenesis and evolution are encouraged. These include reports describing virus morphology, the function and antigenic analysis of virus structural components, virus genome structure and expression, analysis on virus replication processes, virus evolution in connection with antiviral interventions, effects of viruses on their host cells, particularly on the immune system, and the pathogenesis of virus infections, including oncogene activation and transduction.
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