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DC Field | Value | Language |
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dc.contributor.author | Joon Hyung Kim | en_US |
dc.contributor.author | Mamadou Drame | en_US |
dc.contributor.author | Thanyawee Puthanakit | en_US |
dc.contributor.author | Nan Chang Chiu | en_US |
dc.contributor.author | Khuanchai Supparatpinyo | en_US |
dc.contributor.author | Li Min Huang | en_US |
dc.contributor.author | Cheng Hsun Chiu | en_US |
dc.contributor.author | Po Yen Chen | en_US |
dc.contributor.author | Kao Pin Hwang | en_US |
dc.contributor.author | Jasur Danier | en_US |
dc.contributor.author | Damien Friel | en_US |
dc.contributor.author | Bruno Salaun | en_US |
dc.contributor.author | Wayne Woo | en_US |
dc.contributor.author | David W. Vaughn | en_US |
dc.contributor.author | Bruce Innis | en_US |
dc.contributor.author | Anne Schuind | en_US |
dc.date.accessioned | 2022-10-16T07:21:46Z | - |
dc.date.available | 2022-10-16T07:21:46Z | - |
dc.date.issued | 2021-09-01 | en_US |
dc.identifier.issn | 15320987 | en_US |
dc.identifier.issn | 08913668 | en_US |
dc.identifier.other | 2-s2.0-85112751314 | en_US |
dc.identifier.other | 10.1097/INF.0000000000003247 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85112751314&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/77032 | - |
dc.description.abstract | Background: This phase 2 observer-blind, randomized, multicenter, dose-ranging study evaluated immunogenicity and safety of different formulations of an AS03-adjuvanted H5N1 influenza vaccine in children 6-35 months of age. Methods: One hundred eighty-five children randomized into 5 groups [1.9 mg hemagglutinin (HA)/AS03B, 0.9 g HA/AS03C, 1.9 g HA/AS03C, 3.75 mg HA/AS03Cor 3.75 mg HA/AS03D] were to receive 2 doses administered 21 days apart (primary vaccination). AS03 was classified by amount of DL-α-tocopherol, with AS03Bthe highest amount. One year later, all subjects were to receive unadjuvanted 3.75 mg HA as antigen challenge. Immunogenicity was assessed 21 days after primary vaccination (day 42) and 7 days after antigen challenge (day 392). Immunogenicity-fever index, based on hemagglutination inhibition and microneutralization antibody titers at day 42 and fever 7 days after each vaccination, was used to guide the selection of an acceptable formulation. Results: After primary vaccination, formulations elicited strong homologous immune responses with all subjects' hemagglutination inhibition titers ≥1:40 post-vaccination. Immunogenicity-fever index based on hemagglutination inhibition and microneutralization assays showed that 1.9 mg HA/AS03Branked the highest. Antibody levels persisted >4 times above baseline 12 months after primary vaccination with all formulations (day 385). Antibodies increased >4-fold after antigen challenge (day 392/day 385) with 1.9 mg HA/AS03B, 0.9 mg HA/AS03Cand 1.9 mg HA/AS03Cformulations. Overall per subject, the incidence of fever ranged from 28.6% (3.75 mg HA/AS03D) to 60.5% (1.9 mg HA/AS03B). Conclusions: All formulations were highly immunogenic and demonstrated acceptable safety profiles, with the 1.9 mg HA/AS03Bproviding the most favorable balance of immunogenicity versus reactogenicity for use in children 6-35 months of age. | en_US |
dc.subject | Medicine | en_US |
dc.title | Immunogenicity and Safety of AS03-adjuvanted H5N1 Influenza Vaccine in Children 6-35 Months of Age: Results From a Phase 2, Randomized, Observer-blind, Multicenter, Dose-ranging Study | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Pediatric Infectious Disease Journal | en_US |
article.volume | 40 | en_US |
article.stream.affiliations | China Medical University College of Medicine | en_US |
article.stream.affiliations | GlaxoSmithKline Pharmaceuticals SA/NV | en_US |
article.stream.affiliations | GlaxoSmithKline, USA | en_US |
article.stream.affiliations | Chang Gung University College of Medicine | en_US |
article.stream.affiliations | National Taiwan University Hospital | en_US |
article.stream.affiliations | Chulalongkorn University | en_US |
article.stream.affiliations | Veterans General Hospital-Taichung Taiwan | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
article.stream.affiliations | MacKay Children's Hospital | en_US |
article.stream.affiliations | PATH | en_US |
Appears in Collections: | CMUL: Journal Articles |
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