Human monoclonal antibody derived from transchromosomic cattle neutralizes multiple H1 clades of influenza A virus by recognizing a novel conformational epitope in the hemagglutinin head domain

Rongyuan Gao, Chithra C. Sreenivasan, Zizhang Sheng, Ben M. Hause, Bin Zhou, David E. Wentworth, Travis Clement, Dana Rausch, Colin Brunick, Jane Christopher-Hennings, Hua Wu, Christoph L. Bausch, Eddie J. Sullivan, Adam D. Hoppe, Victor C. Huber, Dan Wang, Feng Li

Research output: Contribution to journalArticlepeer-review

6 Scopus citations


Influenza remains a global health risk and challenge. Currently, neuraminidase (NA) inhibitors are extensively used to treat influenza, but their efficacy is compromised by the emergence of drug-resistant variants. Neutralizing antibodies targeting influenza A virus surface glycoproteins are critical components of influenza therapeutic agents and may provide alternative strategies to the existing countermeasures. However, the major hurdle for the extensive application of antibody therapies lies in the difficulty of generating nonimmunogenic antibodies in large quantities rapidly. Here, we report that one human monoclonal antibody (MAb), 53C10, isolated from transchromosomic (Tc) cattle exhibits potent neutralization and hemagglutination inhibition titers against different clades of H1N1 subtype influenza A viruses. In vitro selection of antibody escape mutants revealed that 53C10 recognizes a novel noncontinuous epitope in the hemagglutinin (HA) head domain involving three amino acid residues, glycine (G), serine (S), and glutamic acid (E) at positions 172, 207, and 212, respectively. The results of our experiments supported a critical role for substitution of arginine at position 207 (S207R) in mediating resistance to 53C10, while substitutions at either G172E or E212A did not alter antibody recognition and neutralization. The E212A mutation may provide structural stability for the epitope, while the substitution G172E probably compensates for loss of fitness introduced by S207R. Our results offer novel insights into the mechanism of action of MAb 53C10 and indicate its potential role in therapeutic treatment of H1 influenza virus infection in humans. IMPORTANCE Respiratory diseases caused by influenza viruses still pose a serious concern to global health, and neutralizing antibodies constitute a promising area of antiviral therapeutics. However, the potential application of antibodies is often hampered by the challenge in generating nonimmunogenic antibodies in large scale. In the present study, transchromosomic (Tc) cattle were used for the generation of nonimmunogenic monoclonal antibodies (MAbs), and characterization of such MAbs revealed one monoclonal antibody, 53C10, exhibiting a potent neutralization activity against H1N1 influenza viruses. Further characterization of the neutralization escape mutant generated using this MAb showed that three amino acid substitutions in the HA head domain contributed to the resistance. These findings emphasize the importance of Tc cattle in the production of nonimmunogenic MAbs and highlight the potential of MAb 53C10 in the therapeutic application against H1 influenza virus infection in humans.

Original languageEnglish
Article numbere00945-20
JournalJournal of Virology
Issue number22
StatePublished - Nov 2020

Bibliographical note

Funding Information:
The study was supported in part by the South Dakota Agricultural Experiment Station (3AH-673), National Science Foundation/EPSCoR Cooperative Agreement IIA-1355423, the South Dakota Research and Innovation Center, and BioSNTR. This research was also in part funded by an Institutional Development Award (IDeA) from the National Institute of General Medical Sciences (NIGMS) of the NIH (P20GM103443 to V.C.H.), with additional support from the Division of Basic Biomedical Sciences at USD (to V.C.H.).

Publisher Copyright:
Copyright © 2020 American Society for Microbiology. All Rights Reserved.


  • Epitope
  • Influenza
  • Monoclonal antibodies
  • Neutralizing antibodies

ASJC Scopus subject areas

  • Microbiology
  • Immunology
  • Insect Science
  • Virology


Dive into the research topics of 'Human monoclonal antibody derived from transchromosomic cattle neutralizes multiple H1 clades of influenza A virus by recognizing a novel conformational epitope in the hemagglutinin head domain'. Together they form a unique fingerprint.

Cite this