Progress and Pitfalls in the Quest for Effective SARS-CoV-2 (COVID-19) Vaccines

被引:68
作者
Flanagan, Katie L. [1 ,2 ,3 ,4 ,5 ]
Best, Emma [6 ,7 ]
Crawford, Nigel W. [8 ,9 ]
Giles, Michelle [10 ,11 ]
Koirala, Archana [12 ,13 ,14 ]
Macartney, Kristine [12 ,13 ]
Russell, Fiona [8 ,9 ]
Teh, Benjamin W. [15 ,16 ]
Wen, Sophie C. H. [17 ,18 ]
机构
[1] Launceston Gen Hosp, Dept Infect Dis, Launceston, Tas, Australia
[2] Univ Tasmania, Fac Hlth Sci, Launceston, Tas, Australia
[3] Univ Tasmania, Sch Med, Launceston, Tas, Australia
[4] Royal Melbourne Inst Technol RMIT Univ, Sch Hlth & Biomed Sci, Melbourne, Vic, Australia
[5] Monash Univ, Dept Immunol & Pathol, Melbourne, Vic, Australia
[6] Starship Childrens Hosp, Dept Paediat Infect Dis, Auckland, New Zealand
[7] Univ Aucldand, Dept Paediat Child & Youth Hlth, Auckland, New Zealand
[8] Univ Melbourne, Dept Paediat, Melbourne, Vic, Australia
[9] Royal Childrens Hosp, Murdoch Childrens Res Inst, Immunisat Serv, Melbourne, Vic, Australia
[10] Monash Univ, Dept Obstet & Gynaecol, Melbourne, Vic, Australia
[11] Alfred Hlth, Infect Dis Unit, Melbourne, Vic, Australia
[12] Univ Sydney, Dept Child & Adolescent Hlth, Sydney, NSW, Australia
[13] Natl Ctr Immunisat Res & Surveillance NCIRS, Sydney, NSW, Australia
[14] Nepean Hosp, Dept Infect Dis, Sydney, NSW, Australia
[15] Peter MacCallum Canc Ctr, Dept Infect Dis, Melbourne, Vic, Australia
[16] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Melbourne, Vic, Australia
[17] Queensland Childrens Hosp, Infect Management Prevent Serv, South Brisbane, Qld, Australia
[18] Univ Queensland, Ctr Clin Res UQCCR, Brisbane, Qld, Australia
关键词
antibody dependent enhancement (ADE); adverse events of special interest (AESI); bacillus Calmette-Guerin (BCG); cell mediated immunity; Coalition for Epidemic Preparedness Innovations (CEPI); innate immunity; neutralizing antibodies; spike protein; ACUTE RESPIRATORY SYNDROME; ANTIBODY-DEPENDENT ENHANCEMENT; ORIGINAL ANTIGENIC SIN; IMMUNE-RESPONSE; SARS-COV; NONSPECIFIC PROTECTION; EPIDEMIC PREPAREDNESS; CELL RESPONSES; GENETIC DRIFT; CORONAVIRUS;
D O I
10.3389/fimmu.2020.579250
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
There are currently around 200 SARS-CoV-2 candidate vaccines in preclinical and clinical trials throughout the world. The various candidates employ a range of vaccine strategies including some novel approaches. Currently, the goal is to prove that they are safe and immunogenic in humans (phase 1/2 studies) with several now advancing into phase 2 and 3 trials to demonstrate efficacy and gather comprehensive data on safety. It is highly likely that many vaccines will be shown to stimulate antibody and T cell responses in healthy individuals and have an acceptable safety profile, but the key will be to confirm that they protect against COVID-19. There is much hope that SARS-CoV-2 vaccines will be rolled out to the entire world to contain the pandemic and avert its most damaging impacts. However, in all likelihood this will initially require a targeted approach toward key vulnerable groups. Collaborative efforts are underway to ensure manufacturing can occur at the unprecedented scale and speed required to immunize billions of people. Ensuring deployment also occurs equitably across the globe will be critical. Careful evaluation and ongoing surveillance for safety will be required to address theoretical concerns regarding immune enhancement seen in previous contexts. Herein, we review the current knowledge about the immune response to this novel virus as it pertains to the design of effective and safe SARS-CoV-2 vaccines and the range of novel and established approaches to vaccine development being taken. We provide details of some of the frontrunner vaccines and discuss potential issues including adverse effects, scale-up and delivery.
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页数:24
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