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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/31375
Title: Safety and immune responses following administration of H1N1 live attenuated influenza vaccine in Thais
Authors: Benjaluck Phonrat
Punnee Pitisuttithum
Supat Chamnanchanunt
Pilaipan Puthavathana
Nathamon Ngaosuwankul
Suda Louisirirotchanakul
Jittima Dhitavat
Sit Thirapakpoomanunt
Vichai Chokevivat
Suwit Wibulpolprasert
Mahidol University
Faculty of Medicine, Siriraj Hospital, Mahidol University
Thailand Government Pharmaceutical Organization
Thailand Ministry of Public Health
Keywords: Biochemistry, Genetics and Molecular Biology;Immunology and Microbiology;Medicine;Veterinary
Issue Date: 18-Jan-2013
Citation: Vaccine. Vol.31, No.11 (2013), 1503-1509
Abstract: Background: Emergence and rapid spread of influenza H1N1 virus prompted health authorities to develop a safe and effective influenza vaccine for domestic use. The Thai Government Pharmaceutical Organization (GPO) with technical support from Russia through WHO had prepared a pandemic live attenuated vaccine (PLAIV) using ca-ts attenuated candidate strain A/17/CA/2009/38 (H1N1) for Thais. Methods: Each participant received two doses of intranasal H1N1 vaccine or placebo 21 days apart. All were followed up at 7, 21, 42 and 60 days after first immunization. Blood was drawn for hemagglutination inhibition (HAI) assay from all participants at days 1, 21, 42, and 60 after first immunization. A subset of 40 participants aged 19-49 years was randomly selected for nasal washing at days 1, 21, 42, and 60 to assess IgA using direct enzyme-linked immunosorbent assay (ELISA) along with serum HAI and microneutralization (MN) assay determination. Results: A total of 363 subjects aged 12-75 years were randomized into 2 groups (271 vaccinees:92 placebos). Almost all AEs were mild to moderate. Local reactions were stuffy nose (22.3%), runny nose (25.1%), scratchy throat (27.2%) and sore throat (19.3%). Systemic reactions included headache (21.7%), myalgia (13.8%), fatigue (16.8%) and postnasal drip (19.9%). On day 60, HAI seroconversion rates for vaccine:placebo group were 30.3:6.0 for ITT and 29.4:5.1 for PP analysis. Children showed highest seroconversion rate at 44, but it decreased to 39.4 when all 3 assays (HAI, MN assay and ELISA) from subgroup analysis were considered. Conclusion: The vaccine candidate is safe. The use of more than one assay may be needed for evaluation of immune response because live attenuated vaccines could effectively induce different kinds of responses. Different individuals could also mount different kinds of immune response, even to the same antigen. © 2013 Elsevier Ltd.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84874439244&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/31375
ISSN: 18732518
0264410X
Appears in Collections:Scopus 2011-2015

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