Ultrapotent Human Neutralizing Antibody Repertoires Against Middle East Respiratory Syndrome Coronavirus From a Recovered Patient

  • J Infect Dis. 2018 Sep 8;218(8):1249-1260. doi: 10.1093/infdis/jiy311.
Peihua Niu  1 ,  Senyan Zhang  2 ,  Panpan Zhou  2 ,  Baoying Huang  1 ,  Yao Deng  1 ,  Kun Qin  1 ,  Pengfei Wang  2 ,  Wenling Wang  1 ,  Xinquan Wang  2 ,  Jianfang Zhou  1 ,  Linqi Zhang  2 ,  Wenjie Tan  1
Affiliations
  • 1. MOH Key Laboratory of Medical Virology, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.
  • 2. The Ministry of Education Key Laboratory of Protein Science, Beijing Advanced Innovation Center for Structural Biology, Collaborative Innovation Center for Biotherapy, School of Life Sciences, Tsinghua University, China.
PMID: 29846635 DOI: 10.1093/infdis/jiy311
Abstract

Background: The Middle East respiratory syndrome coronavirus (MERS-CoV) causes severe respiratory Infection with a high (~35%) mortality rate. Neutralizing antibodies targeting the spike of MERS-CoV have been shown to be a therapeutic option for treatment of lethal disease.

Methods: We describe the germline diversity and neutralizing activity of 13 potent human monoclonal antibodies (mAbs) that target the MERS-CoV spike (S) protein. Biological functions were assessed by live MERS-CoV, pseudotype particle and its variants, and structural basis was also determined by crystallographic analysis.

Results: Of the 13 mAbs displaying strong neutralizing activity against MERS-CoV, two with the immunoglobulin heavy-chain variable region (IGHV)1-69-derived heavy chain (named MERS-GD27 and MERS-GD33) showed the most potent neutralizing activity against pseudotyped and live MERS-CoV in vitro. Mutagenesis analysis suggested that MERS-GD27 and MERS-GD33 recognized distinct regions in S glycoproteins, and the combination of 2 mAbs demonstrated a synergistic effect in neutralization against pseudotyped MERS-CoV. The structural basis of MERS-GD27 neutralization and recognition revealed that its epitope almost completely overlapped with the receptor-binding site.

Conclusions: Our data provide new insights into the specific antibody repertoires and the molecular determinants of neutralization during natural MERS-CoV Infection in humans. This finding supports additional efforts to design and develop novel therapies to combat MERS-CoV infections in humans.

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