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Open AccessJournal ArticleDOI

Interpretation of responses and protective levels of antibody against attenuated influenza A viruses using single radial haemolysis.

R. Al-Khayatt, +2 more
- 01 Oct 1984 - 
- Vol. 93, Iss: 2, pp 301-312
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TLDR
Antibody determinations against H3N2 and H1N1 type A influenza viruses were carried out on paired sera obtained from volunteers taking part in influenza virus vaccine studies, using both the haemagglutination-inhibition (HI) and single radial haemolysis (SRH) test.
Abstract
Antibody determinations against H3N2 and H1N1 type A influenza viruses were carried out on paired sera obtained from volunteers taking part in influenza virus vaccine studies, using both the haemagglutination-inhibition (HI) and single radial haemolysis (SRH) test. Good correlation between the HI and SRH test was found for both H3N2 and H1N1 antibody and the zone area increases corresponding to significant SRH antibody rises determined for both virus strains. In both H3N2 and H1N1 vaccine studies, intranasal infection of the volunteers with live attenuated viruses was involved and by the measurement of HI and SRH antibodies prior to and following infection, levels of antibody equating with protection against the infecting viruses could be estimated. For the HI test the antibody titres associated with 50% protection were 42 for H1N1, and 44 for H3N2 viruses; for the SRH test, 50% protection was associated with zone areas of 20.0-25.0 mm2 for both H1N1 and H3N2 viruses.

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Safety and antigenicity of non-adjuvanted and MF59-adjuvanted influenza A/Duck/Singapore/97 (H5N3) vaccine : a randomised trial of two potential vaccines against H5N1 influenza

TL;DR: Addition of MF59 to A/Duck/Singapore/97 vaccines boost the antibody response to protection levels, and these findings have implications for development and assessment of vaccines for future pandemics.
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Immune response after a single vaccination against 2009 influenza A H1N1 in USA: a preliminary report of two randomised controlled phase 2 trials.

TL;DR: One dose of vaccine was highly immunogenic in adults, suggesting that it afforded sufficient protection against this pandemic influenza A H1N1 virus.
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Systematic review and economic decision modelling for the prevention and treatment of influenza A and B

TL;DR: The cost-effectiveness varies markedly between the intervention strategies and target populations and the estimate of cost effectiveness is also sensitive to variations in certain key parameters of the model, for example the proportion of all influenza-like illnesses that are influenza.
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Serologic assays for influenza surveillance, diagnosis and vaccine evaluation

TL;DR: The use of standardized protocols and antibody standards are important steps to improve reproducibility and interlaboratory comparability of results of serologic assays for influenza viruses.
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Influenza Vaccination Strategies: Comparing Inactivated and Live Attenuated Influenza Vaccines

TL;DR: The immunological immune responses elicited by the two vaccines are discussed and future work to better define correlates of protection is discussed, with a focus on the live attenuated vaccines.
References
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Journal ArticleDOI

The role of serum haemagglutination-inhibiting antibody in protection against challenge infection with influenza A2 and B viruses.

TL;DR: The intranasal inoculation of volunteers with living partially attenuated strains of influenza A and B viruses offers a new opportunity to determine the protective effect of serum haemagglutin-inhibiting antibody against a strictly homologous virus.
Journal ArticleDOI

A Single Radial Haemolysis Technique for the Measurement of Influenza Antibody

TL;DR: A single radial haemolysis in geltechnique has been developed for the detection and measurement of antibody to influenza haemagglutinin, which is simple, quick, reproducible, and unaffected by non-specific inhibitors.
Journal ArticleDOI

Inactivated vaccines. 2. Laboratory indices of protection

TL;DR: Prevention of flu-like disease, fever, confinement to bed, and/or seroconversion to Hong Kong was significantly related to post-vaccine A/Hong Kong/68(H3N2) haemagglutination-inhibition (HI) titres and presence of NI antibody, in the absence of HI antibody, significantly reduced the AR to 24%.
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