Potential for developing a SARS-CoV receptor-binding domain (RBD) recombinant protein as a heterologous human vaccine against coronavirus infectious disease (COVID)-19
- PMID: 32298218
- PMCID: PMC7482854
- DOI: 10.1080/21645515.2020.1740560
Potential for developing a SARS-CoV receptor-binding domain (RBD) recombinant protein as a heterologous human vaccine against coronavirus infectious disease (COVID)-19
Abstract
A SARS-CoV receptor-binding domain (RBD) recombinant protein was developed and manufactured under current good manufacturing practices in 2016. The protein, known as RBD219-N1 when formulated on Alhydrogel®, induced high-level neutralizing antibodies and protective immunity with minimal immunopathology in mice after a homologous virus challenge with SARS-CoV (MA15 strain). We examined published evidence in support of whether the SARS-CoV RBD219-N1 could be repurposed as a heterologous vaccine against Coronavirus Infectious Disease (COVID)-19. Our findings include evidence that convalescent serum from SARS-CoV patients can neutralize SARS-CoV-2. Additionally, a review of published studies using monoclonal antibodies (mAbs) raised against SARS-CoV RBD and that neutralizes the SARS-CoV virus in vitro finds that some of these mAbs bind to the receptor-binding motif (RBM) within the RBD, while others bind to domains outside this region within RBD. This information is relevant and supports the possibility of developing a heterologous SARS-CoV RBD vaccine against COVID-19, especially due to the finding that the overall high amino acid similarity (82%) between SARS-CoV and SARS-CoV-2 spike and RBD domains is not reflected in RBM amino acid similarity (59%). However, the high sequence similarity (94%) in the region outside of RBM offers the potential of conserved neutralizing epitopes between both viruses.
Keywords: COVID-19; Heterologous vaccine; SARS; SARS-CoV-2; coronavirus; receptor-binding domain; subunit vaccine.
Figures
Similar articles
-
Targeting SARS-CoV2 Spike Protein Receptor Binding Domain by Therapeutic Antibodies.Biomed Pharmacother. 2020 Oct;130:110559. doi: 10.1016/j.biopha.2020.110559. Epub 2020 Aug 1. Biomed Pharmacother. 2020. PMID: 32768882 Free PMC article. Review.
-
Yeast-expressed SARS-CoV recombinant receptor-binding domain (RBD219-N1) formulated with aluminum hydroxide induces protective immunity and reduces immune enhancement.Vaccine. 2020 Nov 3;38(47):7533-7541. doi: 10.1016/j.vaccine.2020.09.061. Epub 2020 Sep 22. Vaccine. 2020. PMID: 33039209 Free PMC article.
-
A vaccine targeting the RBD of the S protein of SARS-CoV-2 induces protective immunity.Nature. 2020 Oct;586(7830):572-577. doi: 10.1038/s41586-020-2599-8. Epub 2020 Jul 29. Nature. 2020. PMID: 32726802
-
SARS-CoV-2 spike produced in insect cells elicits high neutralization titres in non-human primates.Emerg Microbes Infect. 2020 Dec;9(1):2076-2090. doi: 10.1080/22221751.2020.1821583. Emerg Microbes Infect. 2020. PMID: 32897177 Free PMC article.
-
Identification of Novel Candidate Epitopes on SARS-CoV-2 Proteins for South America: A Review of HLA Frequencies by Country.Front Immunol. 2020 Sep 3;11:2008. doi: 10.3389/fimmu.2020.02008. eCollection 2020. Front Immunol. 2020. PMID: 33013857 Free PMC article. Review.
Cited by
-
Advances in Pathogenesis, Progression, Potential Targets and Targeted Therapeutic Strategies in SARS-CoV-2-Induced COVID-19.Front Immunol. 2022 Apr 5;13:834942. doi: 10.3389/fimmu.2022.834942. eCollection 2022. Front Immunol. 2022. PMID: 35450063 Free PMC article. Review.
-
Efficient Purification of Polyhistidine-Tagged Recombinant Proteins Using Functionalized Corundum Particles.BioTech (Basel). 2023 May 3;12(2):31. doi: 10.3390/biotech12020031. BioTech (Basel). 2023. PMID: 37218748 Free PMC article.
-
Targeting SARS-CoV2 Spike Protein Receptor Binding Domain by Therapeutic Antibodies.Biomed Pharmacother. 2020 Oct;130:110559. doi: 10.1016/j.biopha.2020.110559. Epub 2020 Aug 1. Biomed Pharmacother. 2020. PMID: 32768882 Free PMC article. Review.
-
Developing a low-cost and accessible COVID-19 vaccine for global health.PLoS Negl Trop Dis. 2020 Jul 29;14(7):e0008548. doi: 10.1371/journal.pntd.0008548. eCollection 2020 Jul. PLoS Negl Trop Dis. 2020. PMID: 32726304 Free PMC article. No abstract available.
-
Scalable, methanol-free manufacturing of the SARS-CoV-2 receptor binding domain in engineered Komagataella phaffii.bioRxiv [Preprint]. 2021 Apr 15:2021.04.15.440035. doi: 10.1101/2021.04.15.440035. bioRxiv. 2021. Update in: Biotechnol Bioeng. 2022 Feb;119(2):657-662. doi: 10.1002/bit.27979 PMID: 33880471 Free PMC article. Updated. Preprint.
References
-
- World Health Organization . WHO director-general’s remarks at the media briefing on 2019-nCoV on 11 February 2020. Ed; 2020. [cited 2020 Apr 2]. Available from: https://www.who.int/dg/speeches/detail/who-director-general-s-remarks-at...
-
- Chen WH, Chag SM, Poongavanam MV, Biter AB, Ewere EA, Rezende W, Seid CA, Hudspeth EM, Pollet J, McAtee CP, et al. Optimization of the production process and characterization of the yeast-expressed SARS-CoV Recombinant Receptor-Binding Domain (RBD219-N1), a SARS vaccine candidate. J Pharm Sci. 2017;106(8):1961–70. doi:10.1016/j.xphs.2017.04.037. - DOI - PMC - PubMed
-
- Jiang S, Bottazzi ME, Du L, Lustigman S, Tseng CT, Curti E, Jones K, Zhan B, Hotez PJ.. Roadmap to developing a recombinant coronavirus S protein receptor-binding domain vaccine for severe acute respiratory syndrome. Expert Rev Vaccines. 2012;11(12):1405–13. doi:10.1586/erv.12.126. - DOI - PMC - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous