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Omicron variant susceptibility to neutralizing antibodies induced in children by natural SARS-CoV-2 infection or COVID-19 vaccine.
Chen, Lin-Lei; Chua, Gilbert T; Lu, Lu; Chan, Brian Pui-Chun; Wong, Joshua Sung-Chih; Chow, Calvin Chit-Kwong; Yu, Tak-Ching; Leung, Agnes Sze-Yin; Lam, Shu-Yan; Wong, Tak-Wai; Tsang, Hing-Wai; Wong, Ian Chi-Kei; Chan, Kwok-Hung; Yuen, Kwok-Yung; Ip, Patrick; Kwan, Mike Yat-Wah; To, Kelvin Kai-Wang.
  • Chen LL; State Key Laboratory for Emerging Infectious Diseases, Department of Microbiology, Li Ka Shing Faculty of Medicine, Carol Yu Centre for Infection, The University of Hong Kong, Hong Kong, People's Republic of China.
  • Chua GT; Department of Pediatrics and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, People's Republic of China.
  • Lu L; Department of Pediatrics and Adolescent Medicine, The Hong Kong Children's Hospital, Hong Kong, People's Republic of China.
  • Chan BP; State Key Laboratory for Emerging Infectious Diseases, Department of Microbiology, Li Ka Shing Faculty of Medicine, Carol Yu Centre for Infection, The University of Hong Kong, Hong Kong, People's Republic of China.
  • Wong JS; State Key Laboratory for Emerging Infectious Diseases, Department of Microbiology, Li Ka Shing Faculty of Medicine, Carol Yu Centre for Infection, The University of Hong Kong, Hong Kong, People's Republic of China.
  • Chow CC; Department of Pediatrics and Adolescent Medicine, Princess Margaret Hospital, Hong Kong, People's Republic of China.
  • Yu TC; Department of Pediatrics and Adolescent Medicine, United Christian Hospital, Hong Kong, People's Republic of China.
  • Leung AS; Department of Pediatrics and Adolescent Medicine, Pamela Youde Nethersole Eastern Hospital, Hong Kong, People's Republic of China.
  • Lam SY; Department of Pediatrics, Prince of Wales Hospital, Chinese University of Hong Kong, Hong Kong, People's Republic of China.
  • Wong TW; Department of Pediatrics and Adolescent Medicine, Tuen Mun Hospital, Hong Kong, People's Republic of China.
  • Tsang HW; Department of Pediatrics and Adolescent Medicine, Alice Ho Miu Ling Nethersole Hospital, Hong Kong, People's Republic of China.
  • Wong IC; Department of Pediatrics and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, People's Republic of China.
  • Chan KH; Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, Centre for Safe Medication Practice and Research, The University of Hong Kong, Hong Kong, People's Republic of China.
  • Yuen KY; Laboratory of Data Discovery for Health (D24H), Hong Kong Science and Technology Park, Hong Kong, People's Republic of China.
  • Ip P; School of Pharmacy, Research Department of Practice and Policy, University College London, London, United Kingdom.
  • Kwan MY; State Key Laboratory for Emerging Infectious Diseases, Department of Microbiology, Li Ka Shing Faculty of Medicine, Carol Yu Centre for Infection, The University of Hong Kong, Hong Kong, People's Republic of China.
  • To KK; State Key Laboratory for Emerging Infectious Diseases, Department of Microbiology, Li Ka Shing Faculty of Medicine, Carol Yu Centre for Infection, The University of Hong Kong, Hong Kong, People's Republic of China.
Emerg Microbes Infect ; 11(1): 543-547, 2022 Dec.
Article in English | MEDLINE | ID: covidwho-1655963
ABSTRACT
The novel SARS-CoV-2 Omicron variant may increase the risk of re-infection and vaccine breakthrough infections as it possesses key mutations in the spike protein that affect neutralizing antibody response. Most studies on neutralization susceptibility were conducted using specimens from adult COVID-19 patients or vaccine recipients. However, since the paediatric population has an antibody response to SARS-CoV-2 infection that is distinct from the adult population, it is critical to assess the neutralization susceptibility of pediatric serum specimens. This study compared the neutralization susceptibility of serum specimens collected from 49 individuals of <18 years old, including 34 adolescent BNT162b2 (Pfizer-BioNTech) vaccine recipients, and 15 recovered COVID-19 patients aged between 2 and 17. We demonstrated that only 38.2% of BNT162b2 vaccine recipients and 26.7% of recovered COVID-19 patients had their serum neutralization titre at or above the detection threshold in our live virus microneutralization assay. Furthermore, the neutralizing antibody titer against the Omicron variant was substantially lower than those against the ancestral virus or the Beta variant. Our results suggest that vaccine recipients and COVID-19 patients in the pediatric age group will likely be more susceptible to vaccine breakthrough infections or reinfections due to the Omicron variant than previous variants.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Prognostic study Topics: Vaccines / Variants Limits: Adolescent / Adult / Child / Child, preschool / Humans Language: English Journal: Emerg Microbes Infect Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Prognostic study Topics: Vaccines / Variants Limits: Adolescent / Adult / Child / Child, preschool / Humans Language: English Journal: Emerg Microbes Infect Year: 2022 Document Type: Article