| Literature DB >> 23680121 |
Xiao Zhang1, Xian Qi, Qianqian Zhang, Xiaoyan Zeng, Zhiyang Shi, Qiu Jin, Feng Zhan, Yan Xu, Zhe Liu, Zhenqing Feng, Yongjun Jiao.
Abstract
Influenza A viruses present a significant threat to public health worldwide. High-affinity human scFv antibodies against a conserved epitope can potentially provide immunity to diverse viruses and protect against future pandemic viruses. A library of phage-displayed human scFv containing 6.0×10(8) members was generated from lymphocytes of H5N1 virus vaccinated individuals. Using the recombinant H5N1 virus hemagglutinin ectodomain (HA1), 4F5 scFv was identified with neutralizing activity against both clade 2 and 9 H5N1 viruses. In embryonated chicken eggs, the antiviral activity of 4F5 scFv conferred a 100% survival rate and at least a 62.5% survival rate against different clades of H5N1 viruses by pre-treatment and post-treatment, respectively. 4F5 scFv belongs to the VH-3-43 family according to the IMGT database, and a peptide (76)WLLGNP(81) containing half of an α-helix in HA1 was identified as the binding pocket. The conserved binding epitope of this novel broadly neutralizing scFv may become key in the design and implementation of vaccines or RNA interference against H5N1 viruses.Entities:
Keywords: Antiviral effect; Broad neutralization; Conserved epitope; H5N1 influenza A viruses; α-Helix
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Year: 2013 PMID: 23680121 DOI: 10.1016/j.antiviral.2013.05.001
Source DB: PubMed Journal: Antiviral Res ISSN: 0166-3542 Impact factor: 5.970