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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- 25775.xml