Crowe J E, Gilmour P S, Murphy B R, Chanock R M, Duan L, Pomerantz R J, Pilkington G R
Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
J Infect Dis. 1998 Apr;177(4):1073-6. doi: 10.1086/517397.
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.
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。