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人源单克隆抗体鸡尾酒疗法(CL184)对多种北美蝙蝠狂犬病病毒变种的体内疗效

In Vivo Efficacy of a Cocktail of Human Monoclonal Antibodies (CL184) Against Diverse North American Bat Rabies Virus Variants.

作者信息

Franka Richard, Carson William C, Ellison James A, Taylor Steven T, Smith Todd G, Kuzmina Natalia A, Kuzmin Ivan V, Marissen Wilfred E, Rupprecht Charles E

机构信息

Centers for Disease Control and Prevention, 1600 Clifton Rd, Atlanta, GA 30333, USA.

East Tennessee State University, James H. Quillen College of Medicine, Johnson City, TN 37614, USA.

出版信息

Trop Med Infect Dis. 2017 Sep 20;2(3):48. doi: 10.3390/tropicalmed2030048.

Abstract

Following rabies virus (RABV) exposure, a combination of thorough wound washing, multiple-dose vaccine administration and the local infiltration of rabies immune globulin (RIG) are essential components of modern post-exposure prophylaxis (PEP). Although modern cell-culture-based rabies vaccines are increasingly used in many countries, RIG is much less available. The prohibitive cost of polyclonal serum RIG products has prompted a search for alternatives and design of anti-RABV monoclonal antibodies (MAbs) that can be manufactured on a large scale with a consistent potency and lower production costs. Robust in vitro neutralization activity has been demonstrated for the CL184 MAb cocktail, a 1:1 protein mixture of two human anti-RABV MAbs (CR57/CR4098), against a large panel of RABV isolates. In this study, we used a hamster model to evaluate the efficacy of experimental PEP against a lethal challenge. Various doses of CL184 and commercial rabies vaccine were assessed for the ability to protect against lethal infection with representatives of four distinct bat RABV lineages of public health relevance: silver-haired bat (Ln RABV); western canyon bat (Ph RABV); big brown bat (Ef-w1 RABV) and Mexican free-tailed bat RABV (Tb RABV). 42⁻100% of animals survived bat RABV infection when CL184 (in combination with the vaccine) was administered. A dose-response relationship was observed with decreasing doses of CL184 resulting in increasing mortality. Importantly, CL184 was highly effective in neutralizing and clearing Ph RABV in vivo, even though CR4098 does not neutralize this virus in vitro. By comparison, 19⁻95% survivorship was observed if human RIG (20 IU/kg) and vaccine were used following challenge with different bat viruses. Based on our results, CL184 represents an efficacious alternative for RIG. Both large-scale and lower cost production could ensure better availability and affordability of this critical life-saving biologic in rabies enzootic countries and as such, significantly contribute to the reduction of human rabies deaths globally.

摘要

暴露于狂犬病病毒(RABV)后,彻底清洗伤口、多剂量接种疫苗以及局部浸润注射狂犬病免疫球蛋白(RIG)是现代暴露后预防(PEP)的重要组成部分。尽管现代基于细胞培养的狂犬病疫苗在许多国家越来越多地被使用,但RIG的供应却少得多。多克隆血清RIG产品高昂的成本促使人们寻找替代品,并设计能够大规模生产、效力一致且生产成本较低的抗RABV单克隆抗体(MAb)。CL184 MAb鸡尾酒(两种人源抗RABV MAb(CR57/CR4098)的1:1蛋白质混合物)已被证明对大量RABV分离株具有强大的体外中和活性。在本研究中,我们使用仓鼠模型评估实验性PEP对致死性攻击的疗效。评估了不同剂量的CL184和商业狂犬病疫苗对四种具有公共卫生相关性的不同蝙蝠RABV谱系代表毒株致死性感染的防护能力:银毛蝙蝠(Ln RABV);西部峡谷蝙蝠(Ph RABV);大棕蝠(Ef-w1 RABV)和墨西哥无尾蝙蝠RABV(Tb RABV)。当给予CL184(与疫苗联合使用)时,42%-100%的动物在感染蝙蝠RABV后存活。观察到随着CL184剂量的降低,死亡率增加,呈现剂量反应关系。重要的是,尽管CR4098在体外不能中和这种病毒,但CL184在体内对Ph RABV具有高效的中和和清除作用。相比之下,在用不同蝙蝠病毒攻击后使用人RIG(20 IU/kg)和疫苗时,观察到19%-95%的存活率。基于我们的结果,CL184是RIG的一种有效替代品。大规模且低成本的生产可以确保这种关键的救命生物制品在狂犬病流行国家有更好的可及性和可负担性,从而显著有助于全球范围内减少人类狂犬病死亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80de/6082099/497b29012697/tropicalmed-02-00048-g001.jpg

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