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Real-world COVID-19 vaccine effectiveness against the Omicron BA.2 variant in a SARS-CoV-2 infection-naive population.
Lau, Jonathan J; Cheng, Samuel M S; Leung, Kathy; Lee, Cheuk Kwong; Hachim, Asmaa; Tsang, Leo C H; Yam, Kenny W H; Chaothai, Sara; Kwan, Kelvin K H; Chai, Zacary Y H; Lo, Tiffany H K; Mori, Masashi; Wu, Chao; Valkenburg, Sophie A; Amarasinghe, Gaya K; Lau, Eric H Y; Hui, David S C; Leung, Gabriel M; Peiris, Malik; Wu, Joseph T.
  • Lau JJ; WHO Collaborating Centre for Infectious Disease Epidemiology and Control, School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
  • Cheng SMS; Laboratory of Data Discovery for Health (D24H), Hong Kong SAR, China.
  • Leung K; School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
  • Lee CK; School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
  • Hachim A; WHO Collaborating Centre for Infectious Disease Epidemiology and Control, School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
  • Tsang LCH; Laboratory of Data Discovery for Health (D24H), Hong Kong SAR, China.
  • Yam KWH; School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
  • Chaothai S; The University of Hong Kong - Shenzhen Hospital, Shenzhen, China.
  • Kwan KKH; Hong Kong Red Cross Blood Transfusion Service, Hong Kong SAR, People's Republic of China.
  • Chai ZYH; HKU-Pasteur Research Pole, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
  • Lo THK; School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
  • Mori M; School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
  • Wu C; School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
  • Valkenburg SA; School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
  • Amarasinghe GK; School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
  • Lau EHY; WHO Collaborating Centre for Infectious Disease Epidemiology and Control, School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
  • Hui DSC; Laboratory of Data Discovery for Health (D24H), Hong Kong SAR, China.
  • Leung GM; School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
  • Peiris M; Research Institute for Bioresources and Biotechnology, Ishikawa Prefectural University, Nonoichi, Japan.
  • Wu JT; Department of Pathology and Immunology, Washington University School of Medicine at St. Louis, St. Louis, MO, USA.
Nat Med ; 29(2): 348-357, 2023 02.
Article in English | MEDLINE | ID: covidwho-2185966
ABSTRACT
The SARS-CoV-2 Omicron variant has demonstrated enhanced transmissibility and escape of vaccine-derived immunity. Although first-generation vaccines remain effective against severe disease and death, robust evidence on vaccine effectiveness (VE) against all Omicron infections, irrespective of symptoms, remains sparse. We used a community-wide serosurvey with 5,310 subjects to estimate how vaccination histories modulated risk of infection in infection-naive Hong Kong during a large wave of Omicron BA.2 epidemic in January-July 2022. We estimated that Omicron infected 45% (41-48%) of the local population. Three and four doses of BNT162b2 or CoronaVac were effective against Omicron infection 7 days after vaccination (VE of 48% (95% credible interval 34-64%) and 69% (46-98%) for three and four doses of BNT162b2, respectively; VE of 30% (1-66%) and 56% (6-97%) for three and four doses of CoronaVac, respectively). At 100 days after immunization, VE waned to 26% (7-41%) and 35% (10-71%) for three and four doses of BNT162b2, and to 6% (0-29%) and 11% (0-54%) for three and four doses of CoronaVac. The rapid waning of VE against infection conferred by first-generation vaccines and an increasingly complex viral evolutionary landscape highlight the necessity for rapidly deploying updated vaccines followed by vigilant monitoring of VE.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Type of study: Experimental Studies / Prognostic study Topics: Vaccines / Variants Limits: Humans Language: English Journal: Nat Med Journal subject: Molecular Biology / Medicine Year: 2023 Document Type: Article Affiliation country: S41591-023-02219-5

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Type of study: Experimental Studies / Prognostic study Topics: Vaccines / Variants Limits: Humans Language: English Journal: Nat Med Journal subject: Molecular Biology / Medicine Year: 2023 Document Type: Article Affiliation country: S41591-023-02219-5