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Immune escape and waning immunity of COVID-19 monovalent mRNA vaccines against symptomatic infection with BA.1/BA.2 and BA.5 in Japan.
Arashiro, Takeshi; Arima, Yuzo; Kuramochi, Jin; Muraoka, Hirokazu; Sato, Akihiro; Chubachi, Kumi; Oba, Kunihiro; Yanai, Atsushi; Arioka, Hiroko; Uehara, Yuki; Ihara, Genei; Kato, Yasuyuki; Yanagisawa, Naoki; Nagura, Yoshito; Yanai, Hideki; Ueda, Akihiro; Numata, Akira; Kato, Hideaki; Oka, Hideaki; Nishida, Yusuke; Ishii, Koji; Ooki, Takao; Nidaira, Yuki; Asami, Takahiro; Jinta, Torahiko; Nakamura, Akira; Taniyama, Daisuke; Yamamoto, Kei; Tanaka, Katsushi; Ueshima, Kankuro; Fuwa, Tetsuji; Stucky, Ashley; Suzuki, Tadaki; Smith, Chris; Hibberd, Martin; Ariyoshi, Koya; Suzuki, Motoi.
Afiliação
  • Arashiro T; Center for Surveillance, Immunization, and Epidemiologic Research, National Institute of Infectious Diseases, Tokyo, Japan; Department of Pathology, National Institute of Infectious Diseases, Tokyo, Japan; Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, L
  • Arima Y; Center for Surveillance, Immunization, and Epidemiologic Research, National Institute of Infectious Diseases, Tokyo, Japan.
  • Kuramochi J; Kuramochi Clinic Interpark, Tochigi, Japan; Department of Global Health Promotion, Tokyo Medical and Dental University, Tokyo, Japan.
  • Muraoka H; CLINIC FOR Tamachi, Tokyo, Japan.
  • Sato A; KARADA Internal Medicine Clinic, Tokyo, Japan.
  • Chubachi K; Chubachi Internal Respiratory Medicine Clinic, Tokyo, Japan.
  • Oba K; Department of Pediatrics, Showa General Hospital, Tokyo, Japan.
  • Yanai A; Department of General Internal Medicine, St. Luke's International Hospital, Tokyo, Japan.
  • Arioka H; Department of General Internal Medicine, St. Luke's International Hospital, Tokyo, Japan.
  • Uehara Y; Department of Clinical Laboratory, St. Luke's International Hospital, Tokyo, Japan; Department of Infectious Diseases, Fujita Health University School of Medicine, Aichi, Japan.
  • Ihara G; Machida Ekimae Naika Clinic, Tokyo, Japan.
  • Kato Y; Department of Infectious Diseases, International University of Health and Welfare Narita Hospital, Chiba, Japan.
  • Yanagisawa N; Yanagisawa Clinic, Tokyo, Japan.
  • Nagura Y; Shinjuku Home Clinic, Tokyo, Japan.
  • Yanai H; Fukujuji Hospital, Japan Anti-Tuberculosis Association, Kiyose, Japan.
  • Ueda A; Department of Infectious Diseases, Japanese Red Cross Medical Center, Tokyo, Japan.
  • Numata A; Ikebukuro Metropolitan Clinic, Tokyo, Japan.
  • Kato H; Infection Prevention and Control Department, Yokohama City University Hospital, Yokohama, Japan.
  • Oka H; Department of General Internal Medicine and Infectious Diseases, Saitama Medical Center, Saitama, Japan.
  • Nishida Y; Department of General Internal Medicine and Infectious Diseases, Saitama Medical Center, Saitama, Japan.
  • Ishii K; Saitama Sekishinkai Hospital, Saitama, Japan.
  • Ooki T; Saitama Sekishinkai Hospital, Saitama, Japan.
  • Nidaira Y; Kuramochi Clinic Interpark, Tochigi, Japan.
  • Asami T; Department of Internal Medicine, Sano Kosei General Hospital, Tochigi, Japan.
  • Jinta T; Department of Pulmonary Medicine, St. Luke's International Hospital, Tokyo, Japan.
  • Nakamura A; Department of Internal Medicine, Asahi General Hospital, Chiba, Japan.
  • Taniyama D; Department of Infectious Diseases, Showa General Hospital, Tokyo, Japan.
  • Yamamoto K; Department of General Internal Medicine and Infectious Diseases, Saitama Medical Center, Saitama, Japan.
  • Tanaka K; Infection Prevention and Control Department, Yokohama City University Hospital, Yokohama, Japan.
  • Ueshima K; NATURALI Co., Ltd, Tokyo, Japan.
  • Fuwa T; NATURALI Co., Ltd, Tokyo, Japan.
  • Stucky A; Center for Surveillance, Immunization, and Epidemiologic Research, National Institute of Infectious Diseases, Tokyo, Japan.
  • Suzuki T; Department of Pathology, National Institute of Infectious Diseases, Tokyo, Japan.
  • Smith C; Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom; School of Tropical Medicine and Global Health, Nagasaki University, Nagasaki, Japan.
  • Hibberd M; Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.
  • Ariyoshi K; School of Tropical Medicine and Global Health, Nagasaki University, Nagasaki, Japan.
  • Suzuki M; Center for Surveillance, Immunization, and Epidemiologic Research, National Institute of Infectious Diseases, Tokyo, Japan.
Vaccine ; 41(47): 6969-6979, 2023 11 13.
Article em En | MEDLINE | ID: mdl-37839947
ABSTRACT

BACKGROUND:

Repeated emergence of variants with immune escape capacity and waning immunity from vaccination are major concerns for COVID-19. We examined whether the surge in Omicron subvariant BA.5 cases was due to immune escape or waning immunity through vaccine effectiveness (VE) evaluation.

METHODS:

A test-negative case-control study was conducted in 16 clinics/hospitals during the BA.1/BA.2-dominant and BA.5-dominant periods. VE against symptomatic infection was estimated after adjusting for age, sex, comorbidity, occupation, testing frequency, prior infection, close contact history, clinic/hospital, week, and preventive measures. Absolute VE (aVE) was calculated for 2/3/4 doses, compared to the unvaccinated. Relative VE (rVE) was calculated, comparing 3 vs 2 and 4 vs 3 doses.

RESULTS:

13,025 individuals were tested during the BA.1/BA.2-dominant and BA.5-dominant periods with similar baseline characteristics. For BA.1/BA.2, aVE was 52 % (95 %CI34-66) 14 days-3 months post-dose 2, 42 % (29-52) > 6 months post-dose 2, 71 % (64-77) 14 days-3 months post-dose 3, and 68 % (52-79) 3-6 months post-dose 3. rVE was 49 % (38-57) 14 days-3 months post-dose 3 and 45 % (18-63) 3-6 months post-dose 3. For BA.5, aVE was 56 % (27-73) 3-6 months post-dose 2, 32 % (12-47) > 6 months post-dose 2, 70 % (61-78) 14 days-3 months post-dose 3, 59 % (48-68) 3-6 months post-dose 3, 50 % (29-64) > 6 months post-dose 3, and 74 % (61-83) ≥ 14 days post-dose 4. rVE was 56 % (45-65) 14 days-3 months post-dose 3, 39 % (27-48) 3-6 months post-dose 3, 25 % (-2-45) > 6 months post-dose 3, and 30 % (-6-54) ≥ 14 days post-dose 4.

CONCLUSIONS:

Booster doses initially provided high protection against BA.5 at a level similar to that against BA.1/BA.2. However, the protection seemed shorter-lasting against BA.5, which likely contributed to the surge. Furthermore, rVE post-dose 4 was low even among recent vaccinees. These results support the introduction of variant-containing vaccines and emphasize the need for vaccines with longer duration of protection.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pesquisa Biomédica / COVID-19 Limite: Humans País/Região como assunto: Asia Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pesquisa Biomédica / COVID-19 Limite: Humans País/Região como assunto: Asia Idioma: En Ano de publicação: 2023 Tipo de documento: Article