New insights on possible vaccine development against SARS-CoV-2
In December 2019, a novel virus, namely COVID-19 caused by SARS-CoV-2, developed from Wuhan, (Hubei territory of China) used its viral spike glycoprotein receptor-binding domain (RBD) for the entrance into a host cell by binding with ACE-2 receptor and cause acute respiratory distress syndrome (ARDS...
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Veröffentlicht in: | Life sciences (1973) 2020-11, Vol.260, p.118421-12, Article 118421 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | In December 2019, a novel virus, namely COVID-19 caused by SARS-CoV-2, developed from Wuhan, (Hubei territory of China) used its viral spike glycoprotein receptor-binding domain (RBD) for the entrance into a host cell by binding with ACE-2 receptor and cause acute respiratory distress syndrome (ARDS). Data revealed that the newly emerged SARS-CoV-2 affected more than 24,854,140 people with 838,924 deaths worldwide. Until now, no licensed immunization or drugs are present for the medication of SARS-CoV-2. The present review aims to investigate the latest developments and discuss the candidate antibodies in different vaccine categories to develop a reliable and efficient vaccine against SARS-CoV-2 in a short time duration. Besides, the review focus on the present challenges and future directions, structure, and mechanism of SARS-CoV-2 for a better understanding. Based on data, we revealed that most of the vaccines are focus on targeting the spike protein (S) of COVID-19 to neutralized viral infection and develop long-lasting immunity. Up to phase-1 clinical trials, some vaccines showed the specific antigen-receptor T-cell response, elicit the humoral and immune response, displayed tight binding with human-leukocytes-antigen (HLA), and recognized specific antibodies to provoke long-lasting immunity against SARS-CoV-2.
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•The latest developments and antibodies recommendations for a vaccine formulation against SARS-CoV-2 are studied.•The SARS-CoV-2 shared the more than 80% nucleotide sequence with SARS-CoV-1 and 90% to bat genome.•Over 115 companies started the work on different vaccine candidates to develop a strong vaccine.•Phase-1 clinical trials showed better results in provoking specific humoral and immune responses against SAR-CoV-2.•The ideal vaccine should be simple, easy to administrate, long-lasting, and well-coordinated with targets. |
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ISSN: | 0024-3205 1879-0631 |
DOI: | 10.1016/j.lfs.2020.118421 |