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Consensus summary report for CEPI/BC March 12-13, 2020 meeting: Assessment of risk of disease enhancement with COVID-19 vaccines.
Lambert, Paul-Henri; Ambrosino, Donna M; Andersen, Svein R; Baric, Ralph S; Black, Steven B; Chen, Robert T; Dekker, Cornelia L; Didierlaurent, Arnaud M; Graham, Barney S; Martin, Samantha D; Molrine, Deborah C; Perlman, Stanley; Picard-Fraser, Philip A; Pollard, Andrew J; Qin, Chuan; Subbarao, Kanta; Cramer, Jakob P.
  • Lambert PH; Centre of Vaccinology, University of Geneva, Switzerland.
  • Ambrosino DM; Independent Advisor, Stuart, FL, USA.
  • Andersen SR; Coalition for Epidemic Preparedness Innovations, Oslo, Norway.
  • Baric RS; Department of Epidemiology, Gillings School of Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
  • Black SB; Brighton Collaboration, Task Force for Global Health, Decatur, GA, USA.
  • Chen RT; Brighton Collaboration, Task Force for Global Health, Decatur, GA, USA.
  • Dekker CL; Brighton Collaboration, Task Force for Global Health, Decatur, GA, USA. Electronic address: cdekker@stanford.edu.
  • Didierlaurent AM; Centre of Vaccinology, University of Geneva, Switzerland.
  • Graham BS; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
  • Martin SD; Independent Advisor, Boston, MA, USA.
  • Molrine DC; Independent Advisor, Newton, MA, USA.
  • Perlman S; Department of Microbiology and Immunology, University of Iowa, Iowa City, IA, USA.
  • Picard-Fraser PA; Independent Advisor, Worcester, MA, USA.
  • Pollard AJ; Department of Paediatrics, University of Oxford, United Kingdom.
  • Qin C; Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
  • Subbarao K; WHO Collaborating Centre for Reference and Research on Influenza, Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia.
  • Cramer JP; Coalition for Epidemic Preparedness Innovations, London, United Kingdom.
Vaccine ; 38(31): 4783-4791, 2020 06 26.
Article in English | MEDLINE | ID: covidwho-361290
ABSTRACT
A novel coronavirus (CoV), Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), emerged in late 2019 in Wuhan, China and has since spread as a global pandemic. Safe and effective vaccines are thus urgently needed to reduce the significant morbidity and mortality of Coronavirus Disease 2019 (COVID-19) disease and ease the major economic impact. There has been an unprecedented rapid response by vaccine developers with now over one hundred vaccine candidates in development and at least six having reached clinical trials. However, a major challenge during rapid development is to avoid safety issues both by thoughtful vaccine design and by thorough evaluation in a timely manner. A syndrome of "disease enhancement" has been reported in the past for a few viral vaccines where those immunized suffered increased severity or death when they later encountered the virus or were found to have an increased frequency of infection. Animal models allowed scientists to determine the underlying mechanism for the former in the case of Respiratory syncytial virus (RSV) vaccine and have been utilized to design and screen new RSV vaccine candidates. Because some Middle East respiratory syndrome (MERS) and SARS-CoV-1 vaccines have shown evidence of disease enhancement in some animal models, this is a particular concern for SARS-CoV-2 vaccines. To address this challenge, the Coalition for Epidemic Preparedness Innovations (CEPI) and the Brighton Collaboration (BC) Safety Platform for Emergency vACcines (SPEAC) convened a scientific working meeting on March 12 and 13, 2020 of experts in the field of vaccine immunology and coronaviruses to consider what vaccine designs could reduce safety concerns and how animal models and immunological assessments in early clinical trials can help to assess the risk. This report summarizes the evidence presented and provides considerations for safety assessment of COVID-19 vaccine candidates in accelerated vaccine development.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Viral Vaccines / Coronavirus Infections / Betacoronavirus / Antibodies, Viral Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines Limits: Animals / Humans Language: English Journal: Vaccine Year: 2020 Document Type: Article Affiliation country: J.vaccine.2020.05.064

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Viral Vaccines / Coronavirus Infections / Betacoronavirus / Antibodies, Viral Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines Limits: Animals / Humans Language: English Journal: Vaccine Year: 2020 Document Type: Article Affiliation country: J.vaccine.2020.05.064