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COVID-19 vaccine effectiveness against symptomatic SARS-CoV-2 infection during Delta-dominant and Omicron-dominant periods in Japan: a multi-center prospective case-control study (FASCINATE study).
Arashiro, Takeshi; Arima, Yuzo; Muraoka, Hirokazu; Sato, Akihiro; Oba, Kunihiro; Uehara, Yuki; Arioka, Hiroko; Yanai, Hideki; Kuramochi, Jin; Ihara, Genei; Chubachi, Kumi; Yanagisawa, Naoki; Nagura, Yoshito; Kato, Yasuyuki; Ueda, Akihiro; Numata, Akira; Kato, Hideaki; Ishii, Koji; Ooki, Takao; Oka, Hideaki; Nishida, Yusuke; Stucky, Ashley; Smith, Chris; Hibberd, Martin; Ariyoshi, Koya; Suzuki, Motoi.
  • Arashiro T; Center for Surveillance, Immunization, and Epidemiologic Research, National Institute of Infectious Diseases, Tokyo, Japan.
  • Arima Y; Department of Pathology, National Institute of Infectious Diseases, Tokyo, Japan.
  • Muraoka H; Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.
  • Sato A; School of Tropical Medicine and Global Health, Nagasaki University, Nagasaki, Japan.
  • Oba K; Center for Surveillance, Immunization, and Epidemiologic Research, National Institute of Infectious Diseases, Tokyo, Japan.
  • Uehara Y; CLINIC FOR Tamachi, Tokyo, Japan.
  • Arioka H; KARADA Internal Medicine Clinic, Tokyo, Japan.
  • Yanai H; Department of Pediatrics, Showa General Hospital, Tokyo, Japan.
  • Kuramochi J; Department of Clinical Laboratory, St. Luke's International Hospital, Tokyo, Japan.
  • Ihara G; Department of General Internal Medicine, St. Luke's International Hospital, Tokyo, Japan.
  • Chubachi K; Fukujuji Hospital, Japan Anti-Tuberculosis Association, Kiyose, Japan.
  • Yanagisawa N; Kuramochi Clinic Interpark, Tochigi, Japan.
  • Nagura Y; Machida Ekimae Naika Clinic, Tokyo, Japan.
  • Kato Y; Chubachi Internal Respiratory Medicine Clinic, Tokyo, Japan.
  • Ueda A; Yanagisawa Clinic, Tokyo, Japan.
  • Numata A; Shinjuku Home Clinic, Tokyo, Japan.
  • Kato H; Department of Infectious Diseases, International University of Health and Welfare Narita Hospital, Chiba, Japan.
  • Ishii K; Department of Infectious Diseases, Japanese Red Cross Medical Center, Tokyo, Japan.
  • Ooki T; Ikebukuro Metropolitan Clinic, Tokyo, Japan.
  • Oka H; Infection Prevention and Control Department, Yokohama City University Hospital, Yokohama, Japan.
  • Nishida Y; Saitama Sekishinkai Hospital, Saitama, Japan.
  • Stucky A; Saitama Sekishinkai Hospital, Saitama, Japan.
  • Smith C; Department of General Internal Medicine and Infectious Diseases, Saitama Medical Center, Saitama, Japan.
  • Hibberd M; Department of General Internal Medicine and Infectious Diseases, Saitama Medical Center, Saitama, Japan.
  • Ariyoshi K; Center for Surveillance, Immunization, and Epidemiologic Research, National Institute of Infectious Diseases, Tokyo, Japan.
  • Suzuki M; Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Clin Infect Dis ; 2022 Aug 03.
Article in English | MEDLINE | ID: covidwho-2227627
ABSTRACT

BACKGROUND:

Although several COVID-19 vaccines initially showed high efficacy, there have been concerns due to waning immunity and the emergence of variants with immune escape capacity.

METHODS:

A test-negative design case-control study was conducted in 16 healthcare facilities in Japan during the Delta-dominant period (August-September 2021) and the Omicron-dominant period (January-March 2022). Vaccine effectiveness (VE) against symptomatic SARS-CoV-2 infection was calculated for 2 doses for the Delta-dominant period and 2 or 3 doses for the Omicron-dominant period, compared to unvaccinated individuals.

RESULTS:

The analysis included 5795 individuals with 2595 (44.8%) cases. Among vaccinees, 2242 (55.8%) received BNT162b2 and 1624 (40.4%) received mRNA-1273 at manufacturer-recommended intervals. During the Delta-dominant period, VE was 88% (95% CI 82-93) 14 days-3 months after dose 2 and 87% (95% CI 38-97) 3-6 months after dose 2. During the Omicron-dominant period, VE was 56% (95% CI 37-70) 14 days-3 months since dose 2, 52% (95% CI 40-62) 3-6 months after dose 2, 49% (95% CI 34-61) 6 + months after dose 2, and 74% (95% CI 62-83) 14 + days after dose 3. Restricting to individuals at high risk of severe COVID-19 and additional adjustment for preventive measures (i.e. mask-wearing/high-risk behaviors) yielded similar estimates, respectively.

CONCLUSIONS:

In Japan where most are infection-naïve and strict prevention measures are maintained regardless of vaccination status, 2-dose mRNA vaccines provided high protection against symptomatic infection during the Delta-dominant period and moderate protection during the Omicron-dominant period. Among individuals who received an mRNA booster dose, VE recovered to a high level.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Observational study / Prognostic study Topics: Vaccines / Variants Language: English Journal subject: Communicable Diseases Year: 2022 Document Type: Article Affiliation country: Cid

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Observational study / Prognostic study Topics: Vaccines / Variants Language: English Journal subject: Communicable Diseases Year: 2022 Document Type: Article Affiliation country: Cid