COVID-19 Epidemiology, Immunity, and Vaccine Development in Children: A Review.
Jaime FergieMary M MoranAlejandro CaneShanti PatherӦzlem TüreciAmit SrivastavaPublished in: Vaccines (2022)
Although pediatric populations experienced lower COVID-19 severity and mortality than adults, the epidemiology of this disease continues to evolve. COVID-19 clinical manifestations in pediatrics commonly include fever and cough, but may differ from adults and by variant. Serious complications, including MIS-C, rarely occur. Although early data showed a decreased likelihood of COVID-19 transmission from children versus adults, outbreaks and viral shedding studies support pediatric transmission potential. Children may mount more robust initial immune responses to SARS-CoV-2 versus adults. COVID-19 vaccines with available pediatric data include BNT162b2, mRNA-1273, CoronaVac, and BBIBP-CorV. Depending on age group and jurisdiction, BNT162b2 and mRNA-1273 have received full approval or emergency/conditional authorization in the United States and European Union from 6 months of age. Clinical trials have shown BNT162b2 and mRNA-1273 safety and high efficacy in pediatric populations, with demonstrably noninferior immune responses versus young adults. Real-world studies further support BNT162b2 safety and effectiveness against the Delta variant. mRNA vaccination benefits are considered to outweigh risks, including myocarditis; however, pediatric vaccination rates remain relatively low. Given a growing body of clinical trial and real-world data showing vaccine safety and effectiveness, pediatric vaccination should be prioritized as an important strategy to control the pandemic.
Keyphrases
- sars cov
- coronavirus disease
- young adults
- clinical trial
- immune response
- respiratory syndrome coronavirus
- randomized controlled trial
- risk factors
- systematic review
- emergency department
- electronic health record
- healthcare
- childhood cancer
- toll like receptor
- cardiovascular disease
- climate change
- binding protein
- phase ii
- coronary artery disease
- dendritic cells
- drug administration