Monoclonal antibodies capable of binding SARS-CoV-2 spike protein receptor-binding motif specifically prevent GM-CSF induction. Issue 1 (24th March 2021)
- Record Type:
- Journal Article
- Title:
- Monoclonal antibodies capable of binding SARS-CoV-2 spike protein receptor-binding motif specifically prevent GM-CSF induction. Issue 1 (24th March 2021)
- Main Title:
- Monoclonal antibodies capable of binding SARS-CoV-2 spike protein receptor-binding motif specifically prevent GM-CSF induction
- Authors:
- Qiang, Xiaoling
Zhu, Shu
Li, Jianhua
Chen, Weiqiang
Yang, Huan
Wang, Ping
Tracey, Kevin J
Wang, Haichao - Abstract:
- Abstract: A severe acute respiratory syndrome (SARS)-like coronavirus 2 (SARS-CoV-2) has recently caused a pandemic COVID-19 disease that infected approximately 94 million and killed more than 2, 000, 000 people worldwide. Like the SARS-CoV, SARS-CoV-2 also employs a receptor-binding motif (RBM) of its envelope spike protein for binding the host angiotensin-converting enzyme 2 (ACE2) to gain viral entry. Currently, extensive efforts are being made to produce vaccines against a surface fragment of a SARS-CoV-2, such as the spike protein, in order to boost protective antibodies that can inhibit virus-ACE2 interaction to prevent viral entry. It was previously unknown how spike protein-targeting antibodies would affect innate inflammatory responses to SARS-CoV-2 infections. Here we generated a highly purified recombinant protein corresponding to the RBM of SARS-CoV-2, and used it to screen for cross-reactive monoclonal antibodies (mAbs). We found two RBM-binding mAbs that competitively inhibited its interaction with human ACE2, and specifically blocked the RBM-induced GM-CSF secretion in both human peripheral blood mononuclear cells and murine macrophage cultures. Our findings have suggested a possible strategy to prevent SARS-CoV-2-elicited "cytokine storm, " and revealed a potentially anti-inflammatory and protective mechanism for SARS-CoV-2 spike-based vaccines. Graphical Abstract: SARS-CoV-2 Spike Protein-reactive monoclonal antibodies specifically impaired the viral spikeAbstract: A severe acute respiratory syndrome (SARS)-like coronavirus 2 (SARS-CoV-2) has recently caused a pandemic COVID-19 disease that infected approximately 94 million and killed more than 2, 000, 000 people worldwide. Like the SARS-CoV, SARS-CoV-2 also employs a receptor-binding motif (RBM) of its envelope spike protein for binding the host angiotensin-converting enzyme 2 (ACE2) to gain viral entry. Currently, extensive efforts are being made to produce vaccines against a surface fragment of a SARS-CoV-2, such as the spike protein, in order to boost protective antibodies that can inhibit virus-ACE2 interaction to prevent viral entry. It was previously unknown how spike protein-targeting antibodies would affect innate inflammatory responses to SARS-CoV-2 infections. Here we generated a highly purified recombinant protein corresponding to the RBM of SARS-CoV-2, and used it to screen for cross-reactive monoclonal antibodies (mAbs). We found two RBM-binding mAbs that competitively inhibited its interaction with human ACE2, and specifically blocked the RBM-induced GM-CSF secretion in both human peripheral blood mononuclear cells and murine macrophage cultures. Our findings have suggested a possible strategy to prevent SARS-CoV-2-elicited "cytokine storm, " and revealed a potentially anti-inflammatory and protective mechanism for SARS-CoV-2 spike-based vaccines. Graphical Abstract: SARS-CoV-2 Spike Protein-reactive monoclonal antibodies specifically impaired the viral spike protein-induced GM-CSF secretion by human peripheral blood mononuclear cells. … (more)
- Is Part Of:
- Journal of leukocyte biology. Volume 111:Issue 1(2022)
- Journal:
- Journal of leukocyte biology
- Issue:
- Volume 111:Issue 1(2022)
- Issue Display:
- Volume 111, Issue 1 (2022)
- Year:
- 2022
- Volume:
- 111
- Issue:
- 1
- Issue Sort Value:
- 2022-0111-0001-0000
- Page Start:
- 261
- Page End:
- 267
- Publication Date:
- 2021-03-24
- Subjects:
- GM-CSF -- cytokine antibody array -- surface plasmon resonance -- antibody
Leucocytes -- Periodicals
Reticulo-endothelial system -- Periodicals
571.96 - Journal URLs:
- http://jlb.onlinelibrary.wiley.com/hub/journal/10.1002/(ISSN)1938-3673/ ↗
https://academic.oup.com/jleukbio ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/JLB.3COVCRA0920-628RR ↗
- Languages:
- English
- ISSNs:
- 0741-5400
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5010.305000
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- 26046.xml