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分离出第二种在体内具有治疗效果的重组人呼吸道合胞病毒单克隆抗体片段(Fab RSVF2-5)。

Isolation of a second recombinant human respiratory syncytial virus monoclonal antibody fragment (Fab RSVF2-5) that exhibits therapeutic efficacy in vivo.

作者信息

Crowe J E, Gilmour P S, Murphy B R, Chanock R M, Duan L, Pomerantz R J, Pilkington G R

机构信息

Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.

出版信息

J Infect Dis. 1998 Apr;177(4):1073-6. doi: 10.1086/517397.

Abstract

A second human respiratory syncytial virus (RSV)-neutralizing monoclonal antibody was isolated and its binding site was identified. Fab F2-5 is a broadly reactive fusion (F) protein-specific recombinant Fab generated by antigen selection from a random combinatorial library displayed on the surface of filamentous phage. In an in vitro plaque-reduction test, the Fab RSVF2-5 neutralized the infectivity of a variety of field isolates representing viruses of both RSV subgroups A and B. The Fab recognized an antigenic determinant that differed from the only other human anti-F monoclonal antibody (RSV Fab 19) described thus far. A single dose of 4.0 mg of Fab RSVF2-5/kg of body weight administered by inhalation was sufficient to achieve a 2000-fold reduction in pulmonary virus titer in RSV-infected mice. The antigen-binding domain of Fab RSVF2-5 offers promise as part of a prophylactic regimen for RSV infection in humans.

摘要

分离出第二种人呼吸道合胞病毒(RSV)中和单克隆抗体并确定其结合位点。Fab F2-5是一种具有广泛反应性的融合(F)蛋白特异性重组Fab,通过从丝状噬菌体表面展示的随机组合文库中进行抗原选择产生。在体外蚀斑减少试验中,Fab RSVF2-5中和了代表RSV A和B两个亚组病毒的多种现场分离株的感染性。该Fab识别的抗原决定簇不同于迄今为止描述的唯一另一种人抗F单克隆抗体(RSV Fab 19)。通过吸入给予单剂量4.0 mg Fab RSVF2-5/kg体重足以使RSV感染小鼠的肺部病毒滴度降低2000倍。Fab RSVF2-5的抗原结合域有望作为人类RSV感染预防方案的一部分。

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