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IgA MAb blocks SARS-CoV-2 Spike-ACE2 interaction providing mucosal immunity [preprint]

  • Monir, Ejemel
  • Li, Qi
  • Hou, Shurong
  • Schiller, Zachary
  • Wallace, Aaron
  • Amcheslavsky, Alla
  • Yilmaz, Nese Kurt
  • Toomey, Jacqueline R.
  • Schneider, Ryan
  • Cavacini, Lisa
  • Klempner, Mark S.
  • Schiffer, Celia A.
  • Wang, Yan
Publication Date
May 15, 2020
[email protected]
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COVID-19 caused by SARS-CoV-2 has become a global pandemic requiring the development of interventions for the prevention or treatment to curtail mortality and morbidity. No vaccine to boost mucosal immunity or as a therapeutic has yet been developed to SARS-CoV-2. In this study we discover and characterize a cross-reactive human IgA monoclonal antibody, MAb362. MAb362 binds to both SARS-CoV and SARS-CoV-2 spike proteins and competitively blocks hACE2 receptor binding, by completely overlapping the hACE2 structural binding epitope. Furthermore, MAb362 IgA neutralizes both pseudotyped SARS-CoV and SARS-CoV-2 in human epithelial cells expressing hACE2. SARS-CoV-2 specific IgA antibodies, such as MAb362, may provide effective immunity against SARS-CoV-2 by inducing mucosal immunity within the respiratory system, a potentially critical feature of an effective vaccine.

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