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Dynamic changes in clinical characteristics and serotype distribution of invasive pneumococcal disease among adults in Japan after introduction of the pediatric 13-valent pneumococcal conjugate vaccine in 2013-2019.
Tamura, Kosuke; Chang, Bin; Shimbashi, Reiko; Watanabe, Hiroshi; Tanabe, Yoshinari; Kuronuma, Koji; Oshima, Kengo; Maruyama, Takaya; Fujita, Jiro; Abe, Shuichi; Kasahara, Kei; Nishi, Junichiro; Kubota, Tetsuya; Kinjo, Yuki; Fujikura, Hiroyuki; Fukusumi, Munehisa; Shimada, Tomoe; Sunagawa, Tomimasa; Suzuki, Motoi; Yamamoto, Yoshihiro; Oishi, Kazunori.
Affiliation
  • Tamura K; Department of Research Planning, Toyama Institute of Health, Toyama, Japan.
  • Chang B; Department of Bacteriology I, National Institute of Infectious Diseases, Tokyo, Japan.
  • Shimbashi R; Center for Surveillance, Immunization, and Epidemiologic Research, National Institute of Infectious Diseases, Tokyo, Japan.
  • Watanabe H; Department of Infection Control and Prevention, Kurume University School of Medicine, Fukuoka, Japan.
  • Tanabe Y; Department of Respiratory Medicine, Niigata Prefectural Shibata Hospital, Niigata, Japan.
  • Kuronuma K; Department of Respiratory Medicine and Allergology, Sapporo Medical University School of Medicine, Hokkaido, Japan.
  • Oshima K; Department of Infectious Disease, Tohoku University Graduate School of Medicine, Miyagi, Japan.
  • Maruyama T; Mie Prefectural Ichishi Hospital, Mie, Japan.
  • Fujita J; Department of Infectious, Respiratory and Digestive Medicine, Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.
  • Abe S; Department of Infectious Diseases and Infection Control, Yamagata Prefectural Central Hospital, Japan.
  • Kasahara K; Center for Infectious Diseases, Nara Medical University, Nara, Japan.
  • Nishi J; Department of Microbiology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
  • Kubota T; Department of Respiratory Medicine and Allergology, Kochi Medical School, Kochi University, Kochi, Japan.
  • Kinjo Y; Department of Bacteriology, The Jikei University School of Medicine, Tokyo, Japan.
  • Fujikura H; Center for Infectious Diseases, Nara Medical University, Nara, Japan.
  • Fukusumi M; Center for Field Epidemic Intelligence, Research and Professional Development, National Institute of Infectious Diseases, Tokyo, Japan.
  • Shimada T; Center for Field Epidemic Intelligence, Research and Professional Development, National Institute of Infectious Diseases, Tokyo, Japan.
  • Sunagawa T; Center for Field Epidemic Intelligence, Research and Professional Development, National Institute of Infectious Diseases, Tokyo, Japan.
  • Suzuki M; Center for Surveillance, Immunization, and Epidemiologic Research, National Institute of Infectious Diseases, Tokyo, Japan.
  • Yamamoto Y; Department of Clinical Infectious Diseases, Toyama University Graduate School of Medicine and Pharmaceutical Sciences, Toyama, Japan.
  • Oishi K; Department of Bacteriology, Toyama Institute of Health, Toyama, Japan. Electronic address: toyamaeiken1@chic.ocn.ne.jp.
Vaccine ; 40(24): 3338-3344, 2022 05 26.
Article in En | MEDLINE | ID: mdl-35489986
ABSTRACT
Nationwide population-based surveillance for invasive pneumococcal disease (IPD) is being conducted in few Asian countries. We aimed to evaluate the clinical characteristics and serotype distribution among Japanese adult patients with IPD after introduction of the pediatric 13-valent pneumococcal conjugate vaccine (PCV13) in 2013. IPD surveillance was conducted among adults between 2013 and 2019, and 1,995 patients were analyzed by time period (early, 2013-2015; middle, 2016-2017; late, 2018-2019). We found that the period of 2018-2019 was independently associated with a lower risk of fatal outcome, compared with the period of 2013-2015. The proportion of those with serotype PCV13-nonPCV7 decreased significantly in patients aged 15-64 years and in those aged ≥ 65 years within 3 years after the introduction of pediatric PCV13. By contrast, the proportion of those with nonvaccine serotype increased significantly in those aged ≥ 65 years, but not in those aged 15-64 years. No significant change was found in the proportion of 23-valent polysaccharide pneumococcal vaccine (PPSV23)-nonPCV13 in both of adults aged 15-64 years and ≥ 65 years. The proportions of PCV15-, PCV20- and PCV24-covered serotypes were 38%, 56% and 58% in adult patients with IPD aged ≥ 65 years during the late period. Our data on the serotype distribution support an indirect effect from pediatric PCV13 use among adults, and afford a basis for estimates of protection against IPD by vaccination with newly developed PCVs in older adults in Japan.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pneumococcal Infections / Pneumococcal Vaccines Limits: Aged / Child / Humans / Infant Country/Region as subject: Asia Language: En Journal: Vaccine Year: 2022 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pneumococcal Infections / Pneumococcal Vaccines Limits: Aged / Child / Humans / Infant Country/Region as subject: Asia Language: En Journal: Vaccine Year: 2022 Document type: Article Affiliation country: