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  1. Article: Screening interval for diabetic retinopathy: a personalised approach (abridged secondary publication).

    Lian, J / Lam, C L K / Thach, T Q / McGhee, S / Fung, C S C / Kwong, A S K / Chau, C K V / Chan, J C H

    Hong Kong medical journal = Xianggang yi xue za zhi

    2023  Volume 29 Suppl 3, Issue 3, Page(s) 33–35

    MeSH term(s) Humans ; Diabetic Retinopathy/diagnosis ; Diabetes Mellitus, Type 2/complications ; Mass Screening
    Language English
    Publishing date 2023-06-26
    Publishing country China
    Document type Journal Article
    ZDB-ID 1239255-8
    ISSN 1024-2708
    ISSN 1024-2708
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Cross-clade immunogenicity and safety of an AS03A-adjuvanted prepandemic H5N1 influenza vaccine in Hong Kong.

    Chu, D W S / Kwong, A S K / Tsui, W W S / Wang, J H L / Ngai, C K H / Wan, P K T / Ong, G / Tang, H W / Roman, F / Dram, M / Bock, H L

    Hong Kong medical journal = Xianggang yi xue za zhi

    2011  Volume 17, Issue 1, Page(s) 39–46

    Abstract: Objective: To present Hong Kong'Äìspecific data from a large Asian population (also involving Thailand, Singapore, and Taiwan) on safety and manufacturing consistency across four AS03(A)-adjuvanted H5N1 vaccine formulations in terms of immune response ... ...

    Abstract Objective: To present Hong Kong'Äìspecific data from a large Asian population (also involving Thailand, Singapore, and Taiwan) on safety and manufacturing consistency across four AS03(A)-adjuvanted H5N1 vaccine formulations in terms of immune response against the A/Vietnam/1194/2004 strain. Immunogenicity against the heterologous A/Indonesia/05/2005 strain was also assessed. NCT Number: 00449670.
    Design: Prospective, observer-blind study.
    Setting: Out-patient clinic of a tertiary hospital in Hong Kong.
    Participants: A total of 360 subjects aged 18 to 60 years were randomised into six groups to receive two doses (21 days apart) of the study vaccine.
    Interventions: One of the four adjuvanted formulations (3.75 microgram H5N1 haemagglutinin [HA]+AS03(A)) of the vaccine (H5N1-AS03(A)) or one of the two non-adjuvanted (3.75 microgram H5N1 [HA]) formulations of the vaccine (H5N1-DIL).
    Main outcome measures: Blood samples collected before vaccination and 21 days after each vaccine dose were analysed using haemagglutination-inhibition and neutralisation assays. Solicited, unsolicited, and serious adverse events were recorded.
    Results: Manufacturing consistency across all four vaccine formulations was demonstrated. After two doses, the AS03(A)-adjuvanted prepandemic influenza vaccine demonstrated high seroprotection rates against the A/Vietnam/1194/2004 strain (95.8%) and good immunogenicity against the heterologous A/Indonesia/05/2005 strain (45.7%), as compared to the non-adjuvanted vaccine (4.6% and 1.5%, respectively). The seroconversion rates induced by the adjuvanted formulations in terms of viral neutralising antibodies against the two strains were much higher than those induced by the non-adjuvanted formulations. There were no safety concerns for any of the adjuvanted vaccine formulations.
    Conclusions: The AS03(A)-adjuvanted H5N1 prepandemic influenza vaccine demonstrated good immunogenicity and an acceptable safety profile in Hong Kong.
    MeSH term(s) Adult ; Antibodies, Viral/blood ; Female ; Hong Kong ; Humans ; Influenza A Virus, H5N1 Subtype/immunology ; Influenza Vaccines/adverse effects ; Influenza Vaccines/immunology ; Male ; Pandemics ; Prospective Studies
    Chemical Substances Antibodies, Viral ; Influenza Vaccines
    Language English
    Publishing date 2011-02
    Publishing country China
    Document type Journal Article ; Multicenter Study ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 1239255-8
    ISSN 1024-2708
    ISSN 1024-2708
    Database MEDical Literature Analysis and Retrieval System OnLINE

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