tetano
Editor, Senior Moderator
Sheng Wu Gong Cheng Xue Bao
. 2022 Jan 25;38(1):160-173.
doi: 10.13345/j.cjb.210173.
[Characterization of a monoclonal antibody against the hemagglutinin stem of H7N9 subtype avian influenza virus]
[Article in Chinese]
Jiangyan Zhao[SUP] 1 2 [/SUP], Yanxiao Zhu[SUP] 1 2 [/SUP], Jiao Hu[SUP] 1 2 [/SUP], Zenglei Hu[SUP] 1 2 3 4 [/SUP], Xiufan Liu[SUP] 1 2 3 4 [/SUP]
Affiliations
Abstract
The conserved hemagglutinin (HA) stem region of avian influenza virus (AIV) is an important target for designing broad-spectrum vaccines, therapeutic antibodies and diagnostic reagents. Previously, we obtained a monoclonal antibody (mAb) (5D3-1B5) which was reactive with the HA stem epitope (aa 428-452) of H7N9 subtype AIV. To systematically characterize the mAb, we determined the antibody titers, including the HA-binding IgG, hemagglutination-inhibition (HI) and virus neutralizing (VN) titers. In addition, the antigenic epitope recognized by the antibody as well as the sequence and structure of the antibody variable region (VR) were also determined. Moreover, we evaluated the cross-reactivity of the antibody with influenza virus strains of different subtypes. The results showed that the 5D3-1B5 antibody had undetectable HI and VN activities against H7N9 virus, whereas it exhibited strong reactivity with the HA protein. Using the peptide-based enzyme-linked immunosorbent assay and biopanning with a phage-displayed random peptide library, a motif with the core sequence ([SUP]431[/SUP]W-[SUP]433[/SUP]Y-[SUP]437[/SUP]L) in the C-helix domain in the HA stem was identified as the epitope recognized by 5D3-1B5. Moreover, the mAb failed to react with the mutant H7N9 virus which contains mutations in the epitope. The VR of the antibody was sequenced and the complementarity determining regions in the VR of the light and heavy chains were determined. Structural modeling and molecular docking analysis of the VR verified specific binding between the antibody and the C-helix domain of the HA stem. Notably, 5D3-1B5 showed a broad cross-reactivity with influenza virus strains of different subtypes belonging to groups 1 and 2. In conclusion, 5D3-1B5 antibody is a promising candidate in terms of the development of broad-spectrum virus diagnostic reagents and therapeutic antibodies. Our findings also provided new information for understanding the epitope characteristics of the HA protein of H7N9 subtype AIV.
Keywords: antigenic epitope; avian influenza virus; cross-reactivity; hemagglutinin stem; monoclonal antibody.
. 2022 Jan 25;38(1):160-173.
doi: 10.13345/j.cjb.210173.
[Characterization of a monoclonal antibody against the hemagglutinin stem of H7N9 subtype avian influenza virus]
[Article in Chinese]
Jiangyan Zhao[SUP] 1 2 [/SUP], Yanxiao Zhu[SUP] 1 2 [/SUP], Jiao Hu[SUP] 1 2 [/SUP], Zenglei Hu[SUP] 1 2 3 4 [/SUP], Xiufan Liu[SUP] 1 2 3 4 [/SUP]
Affiliations
- PMID: 35142127
- DOI: 10.13345/j.cjb.210173
Abstract
The conserved hemagglutinin (HA) stem region of avian influenza virus (AIV) is an important target for designing broad-spectrum vaccines, therapeutic antibodies and diagnostic reagents. Previously, we obtained a monoclonal antibody (mAb) (5D3-1B5) which was reactive with the HA stem epitope (aa 428-452) of H7N9 subtype AIV. To systematically characterize the mAb, we determined the antibody titers, including the HA-binding IgG, hemagglutination-inhibition (HI) and virus neutralizing (VN) titers. In addition, the antigenic epitope recognized by the antibody as well as the sequence and structure of the antibody variable region (VR) were also determined. Moreover, we evaluated the cross-reactivity of the antibody with influenza virus strains of different subtypes. The results showed that the 5D3-1B5 antibody had undetectable HI and VN activities against H7N9 virus, whereas it exhibited strong reactivity with the HA protein. Using the peptide-based enzyme-linked immunosorbent assay and biopanning with a phage-displayed random peptide library, a motif with the core sequence ([SUP]431[/SUP]W-[SUP]433[/SUP]Y-[SUP]437[/SUP]L) in the C-helix domain in the HA stem was identified as the epitope recognized by 5D3-1B5. Moreover, the mAb failed to react with the mutant H7N9 virus which contains mutations in the epitope. The VR of the antibody was sequenced and the complementarity determining regions in the VR of the light and heavy chains were determined. Structural modeling and molecular docking analysis of the VR verified specific binding between the antibody and the C-helix domain of the HA stem. Notably, 5D3-1B5 showed a broad cross-reactivity with influenza virus strains of different subtypes belonging to groups 1 and 2. In conclusion, 5D3-1B5 antibody is a promising candidate in terms of the development of broad-spectrum virus diagnostic reagents and therapeutic antibodies. Our findings also provided new information for understanding the epitope characteristics of the HA protein of H7N9 subtype AIV.
Keywords: antigenic epitope; avian influenza virus; cross-reactivity; hemagglutinin stem; monoclonal antibody.