Vaccines for COVID‐19
The spread of the virus SARS‐CoV‐2, the cause of COVID‐19 has triggered a tidal wave of vaccine development. In the first 9 months since the virus emerged over 200 vaccines have begun pre‐clinical development, 36 of which have entered clinical trials. This review will cover the platforms under asses...
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Veröffentlicht in: | Clinical and experimental immunology 2020-11, Vol.202 (2), p.162-192 |
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creator | Tregoning, J. S. Brown, E. S. Cheeseman, H. M. Flight, K. E. Higham, S. L. Lemm, N.‐M. Pierce, B. F. Stirling, D. C. Wang, Z. Pollock, K. M. |
description | The spread of the virus SARS‐CoV‐2, the cause of COVID‐19 has triggered a tidal wave of vaccine development. In the first 9 months since the virus emerged over 200 vaccines have begun pre‐clinical development, 36 of which have entered clinical trials. This review will cover the platforms under assessment, the immune responses underpinning the vaccines, the results so far and the considerations for the next steps.
Summary
Since the emergence of COVID‐19, caused by the SARS‐CoV‐2 virus at the end of 2019, there has been an explosion of vaccine development. By 24 September 2020, a staggering number of vaccines (more than 200) had started preclinical development, of which 43 had entered clinical trials, including some approaches that have not previously been licensed for human vaccines. Vaccines have been widely considered as part of the exit strategy to enable the return to previous patterns of working, schooling and socializing. Importantly, to effectively control the COVID‐19 pandemic, production needs to be scaled‐up from a small number of preclinical doses to enough filled vials to immunize the world’s population, which requires close engagement with manufacturers and regulators. It will require a global effort to control the virus, necessitating equitable access for all countries to effective vaccines. This review explores the immune responses required to protect against SARS‐CoV‐2 and the potential for vaccine‐induced immunopathology. We describe the profile of the different platforms and the advantages and disadvantages of each approach. The review also addresses the critical steps between promising preclinical leads and manufacturing at scale. The issues faced during this pandemic and the platforms being developed to address it will be invaluable for future outbreak control. Nine months after the outbreak began we are at a point where preclinical and early clinical data are being generated for the vaccines; an overview of this important area will help our understanding of the next phases. |
doi_str_mv | 10.1111/cei.13517 |
format | Article |
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Summary
Since the emergence of COVID‐19, caused by the SARS‐CoV‐2 virus at the end of 2019, there has been an explosion of vaccine development. By 24 September 2020, a staggering number of vaccines (more than 200) had started preclinical development, of which 43 had entered clinical trials, including some approaches that have not previously been licensed for human vaccines. Vaccines have been widely considered as part of the exit strategy to enable the return to previous patterns of working, schooling and socializing. Importantly, to effectively control the COVID‐19 pandemic, production needs to be scaled‐up from a small number of preclinical doses to enough filled vials to immunize the world’s population, which requires close engagement with manufacturers and regulators. It will require a global effort to control the virus, necessitating equitable access for all countries to effective vaccines. This review explores the immune responses required to protect against SARS‐CoV‐2 and the potential for vaccine‐induced immunopathology. We describe the profile of the different platforms and the advantages and disadvantages of each approach. The review also addresses the critical steps between promising preclinical leads and manufacturing at scale. The issues faced during this pandemic and the platforms being developed to address it will be invaluable for future outbreak control. Nine months after the outbreak began we are at a point where preclinical and early clinical data are being generated for the vaccines; an overview of this important area will help our understanding of the next phases.</description><identifier>ISSN: 0009-9104</identifier><identifier>EISSN: 1365-2249</identifier><identifier>DOI: 10.1111/cei.13517</identifier><identifier>PMID: 32935331</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Betacoronavirus - physiology ; Clinical trials ; Clinical Trials as Topic ; Collection: COVID‐19 ; Coronavirus Infections - immunology ; Coronavirus Infections - prevention & control ; COVID-19 ; COVID-19 Vaccines ; Humans ; Immune response ; Pandemics ; Pandemics - prevention & control ; Pneumonia, Viral - immunology ; Pneumonia, Viral - prevention & control ; Review ; SARS-CoV-2 ; Severe acute respiratory syndrome coronavirus 2 ; Vaccination ; Vaccine development ; Vaccines ; Viral Vaccines - immunology</subject><ispartof>Clinical and experimental immunology, 2020-11, Vol.202 (2), p.162-192</ispartof><rights>2020 The Authors. Clinical and Experimental Immunology published by John Wiley & Sons Ltd on behalf of British Society for Immunology</rights><rights>2020 The Authors. Clinical and Experimental Immunology published by John Wiley & Sons Ltd on behalf of British Society for Immunology.</rights><rights>2020. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 The Authors. published by John Wiley & Sons Ltd on behalf of British Society for Immunology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4437-cd6694bcf75ca92663fbb0ef6130bf2347b6c8cc00100d050e8275bd4c884c513</citedby><cites>FETCH-LOGICAL-c4437-cd6694bcf75ca92663fbb0ef6130bf2347b6c8cc00100d050e8275bd4c884c513</cites><orcidid>0000-0002-8098-7161 ; 0000-0001-8093-8741 ; 0000-0002-0834-5201 ; 0000-0001-9513-5183 ; 0000-0003-3841-6864 ; 0000-0003-4139-7780 ; 0000-0001-9044-1341 ; 0000-0002-1110-808X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7597597/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7597597/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32935331$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tregoning, J. S.</creatorcontrib><creatorcontrib>Brown, E. S.</creatorcontrib><creatorcontrib>Cheeseman, H. M.</creatorcontrib><creatorcontrib>Flight, K. E.</creatorcontrib><creatorcontrib>Higham, S. L.</creatorcontrib><creatorcontrib>Lemm, N.‐M.</creatorcontrib><creatorcontrib>Pierce, B. F.</creatorcontrib><creatorcontrib>Stirling, D. C.</creatorcontrib><creatorcontrib>Wang, Z.</creatorcontrib><creatorcontrib>Pollock, K. M.</creatorcontrib><title>Vaccines for COVID‐19</title><title>Clinical and experimental immunology</title><addtitle>Clin Exp Immunol</addtitle><description>The spread of the virus SARS‐CoV‐2, the cause of COVID‐19 has triggered a tidal wave of vaccine development. In the first 9 months since the virus emerged over 200 vaccines have begun pre‐clinical development, 36 of which have entered clinical trials. This review will cover the platforms under assessment, the immune responses underpinning the vaccines, the results so far and the considerations for the next steps.
Summary
Since the emergence of COVID‐19, caused by the SARS‐CoV‐2 virus at the end of 2019, there has been an explosion of vaccine development. By 24 September 2020, a staggering number of vaccines (more than 200) had started preclinical development, of which 43 had entered clinical trials, including some approaches that have not previously been licensed for human vaccines. Vaccines have been widely considered as part of the exit strategy to enable the return to previous patterns of working, schooling and socializing. Importantly, to effectively control the COVID‐19 pandemic, production needs to be scaled‐up from a small number of preclinical doses to enough filled vials to immunize the world’s population, which requires close engagement with manufacturers and regulators. It will require a global effort to control the virus, necessitating equitable access for all countries to effective vaccines. This review explores the immune responses required to protect against SARS‐CoV‐2 and the potential for vaccine‐induced immunopathology. We describe the profile of the different platforms and the advantages and disadvantages of each approach. The review also addresses the critical steps between promising preclinical leads and manufacturing at scale. The issues faced during this pandemic and the platforms being developed to address it will be invaluable for future outbreak control. 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E.</au><au>Higham, S. L.</au><au>Lemm, N.‐M.</au><au>Pierce, B. F.</au><au>Stirling, D. C.</au><au>Wang, Z.</au><au>Pollock, K. M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vaccines for COVID‐19</atitle><jtitle>Clinical and experimental immunology</jtitle><addtitle>Clin Exp Immunol</addtitle><date>2020-11</date><risdate>2020</risdate><volume>202</volume><issue>2</issue><spage>162</spage><epage>192</epage><pages>162-192</pages><issn>0009-9104</issn><eissn>1365-2249</eissn><abstract>The spread of the virus SARS‐CoV‐2, the cause of COVID‐19 has triggered a tidal wave of vaccine development. In the first 9 months since the virus emerged over 200 vaccines have begun pre‐clinical development, 36 of which have entered clinical trials. This review will cover the platforms under assessment, the immune responses underpinning the vaccines, the results so far and the considerations for the next steps.
Summary
Since the emergence of COVID‐19, caused by the SARS‐CoV‐2 virus at the end of 2019, there has been an explosion of vaccine development. By 24 September 2020, a staggering number of vaccines (more than 200) had started preclinical development, of which 43 had entered clinical trials, including some approaches that have not previously been licensed for human vaccines. Vaccines have been widely considered as part of the exit strategy to enable the return to previous patterns of working, schooling and socializing. Importantly, to effectively control the COVID‐19 pandemic, production needs to be scaled‐up from a small number of preclinical doses to enough filled vials to immunize the world’s population, which requires close engagement with manufacturers and regulators. It will require a global effort to control the virus, necessitating equitable access for all countries to effective vaccines. This review explores the immune responses required to protect against SARS‐CoV‐2 and the potential for vaccine‐induced immunopathology. We describe the profile of the different platforms and the advantages and disadvantages of each approach. The review also addresses the critical steps between promising preclinical leads and manufacturing at scale. The issues faced during this pandemic and the platforms being developed to address it will be invaluable for future outbreak control. Nine months after the outbreak began we are at a point where preclinical and early clinical data are being generated for the vaccines; an overview of this important area will help our understanding of the next phases.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>32935331</pmid><doi>10.1111/cei.13517</doi><tpages>31</tpages><orcidid>https://orcid.org/0000-0002-8098-7161</orcidid><orcidid>https://orcid.org/0000-0001-8093-8741</orcidid><orcidid>https://orcid.org/0000-0002-0834-5201</orcidid><orcidid>https://orcid.org/0000-0001-9513-5183</orcidid><orcidid>https://orcid.org/0000-0003-3841-6864</orcidid><orcidid>https://orcid.org/0000-0003-4139-7780</orcidid><orcidid>https://orcid.org/0000-0001-9044-1341</orcidid><orcidid>https://orcid.org/0000-0002-1110-808X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Betacoronavirus - physiology Clinical trials Clinical Trials as Topic Collection: COVID‐19 Coronavirus Infections - immunology Coronavirus Infections - prevention & control COVID-19 COVID-19 Vaccines Humans Immune response Pandemics Pandemics - prevention & control Pneumonia, Viral - immunology Pneumonia, Viral - prevention & control Review SARS-CoV-2 Severe acute respiratory syndrome coronavirus 2 Vaccination Vaccine development Vaccines Viral Vaccines - immunology |
title | Vaccines for COVID‐19 |
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