COVID-19 vaccines: where we stand and challenges ahead

被引:498
|
作者
Forni, Guido [1 ]
Mantovani, Alberto [2 ,3 ]
机构
[1] Acad Nazl Lincei, Via Lungara 10, I-00165 Rome, Italy
[2] Humanitas Univ, Ist Clin Humanitas IRCCS, Via Rita Levi Montalcini 4, I-20090 Milan, Italy
[3] Queen Mary Univ London, William Harvey Res Inst, Charterhouse Sq, London EC1M 6BQ, England
来源
CELL DEATH AND DIFFERENTIATION | 2021年 / 28卷 / 02期
关键词
SARS-COV-2; SPIKE; VACCINATION; INFECTION; STATES; TRIAL;
D O I
10.1038/s41418-020-00720-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the eleven months elapsed since the identification of the SARS-CoV-2 virus and its genome, an exceptional effort by the scientific community has led to the development of over 300 vaccine projects. Over 40 are now undergoing clinical evaluation, ten of these are in Phase III clinical trials, three of them have ended Phase III with positive results. A few of these new vaccines are being approved for emergency use. Existing data suggest that new vaccine candidates may be instrumental in protecting individuals and reducing the spread of pandemic. The conceptual and technological platforms exploited are diverse, and it is likely that different vaccines will show to be better suited to distinct groups of the human population. Moreover, it remains to be elucidated whether and to what extent the capacity of vaccines under evaluation and of unrelated vaccines such as BCG can increase immunological fitness by training innate immunity to SARS-CoV-2 and pathogen-agnostic protection. Due to the short development time and the novelty of the technologies adopted, these vaccines will be deployed with several unresolved issues that only the passage of time will permit to clarify. Technical problems connected with the production of billions of doses and ethical ones connected with the availably of these vaccines also in the poorest countries, are imminent challenges facing us. It is our tenet that in the long run more than one vaccine will be needed to ensure equitable global access, protection of diverse subjects and immunity against viral variants.
引用
收藏
页码:626 / 639
页数:14
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