| Literature DB >> 34033735 |
Kimiko Kawata1, Sheikh Ariful Hoque2,3, Shuichi Nishimura4, Fumihiro Yagyu2, Mohammad Tajul Islam5, Laila Shamima Sharmin6, Ngan Thi Kim Pham2, Yuko Onda-Shimizu2, Trinh Duy Quang2, Sayaka Takanashi7, Shoko Okitsu2, Pattara Khamrin8, Niwat Maneekarn8, Satoshi Hayakawa2, Hiroshi Ushijima2.
Abstract
Although two live oral rotavirus (RV) vaccines, Rotarix and RotaTeq, play a critical role toward reducing disease severity, hospitalization, and death rate in RV infections, regular monitoring of vaccine effectiveness (VE) is yet necessary because the segmented genome structure and reassortment capability of RVs pose considerable threats toward waning VE. In this study, we examined the VE by a test-negative study design against G9P[8]I2 strain during a seasonal outbreak in February-May, 2018, in an outpatient clinic in Kyoto Prefecture, Japan. It remains important because G9P[8]I2 strain remains partially heterotypic to these vaccines and predominating in post-vaccination era. During year-long surveillance, RV infections were detected only from February to May. During this outbreak, 33 (42.3%) children out of 78 with acute gastroenteritis (AGE) remained RV-positive, of which 29 (87.8%) children were infected with G9P[8]I2. Two immunochromatographic (IC) assay kits exhibited 100% sensitivity and specificity to detect G9P[8]I2 strain. Only 23.2% children were found to be vaccinated. Yet, significant VE 69.7% (95% CI: 2.5%-90.6%) was recognized against all RV strains that increased with disease severity. Similar significant VE 71.8% (95% CI: 1%-92%) was determined against G9P[8]I2 strain. The severity score remained substantially low in vaccinated children. Our data reveal that vaccine-preventable G9P[8]I2 strain yet may cause outbreak where vaccination coverage remains low. Thus, this study emphasizes the necessity of global introduction of RV-vaccines in national immunization programs of every country.Entities:
Keywords: Effectiveness; G9P[8]I2; Japan; Rotavirus; vaccine
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Year: 2021 PMID: 34033735 PMCID: PMC8437538 DOI: 10.1080/21645515.2021.1925060
Source DB: PubMed Journal: Hum Vaccin Immunother ISSN: 2164-5515 Impact factor: 4.526