Effectiveness of trivalent seasonal influenza vaccine in preventing laboratory-confirmed influenza in primary care in the United Kingdom: 2012/13 end of season results
Identifieur interne : 000119 ( France/Analysis ); précédent : 000118; suivant : 000120Effectiveness of trivalent seasonal influenza vaccine in preventing laboratory-confirmed influenza in primary care in the United Kingdom: 2012/13 end of season results
Auteurs : N. Andrews ; J. Mcmenamin ; H. Durnall ; J. Ellis ; A. Lackenby ; C. Robertson [France] ; B. Wissmann ; S. Cottrell ; B. Smyth ; C. Moore ; R. Gunson ; M. Zambon ; D. Fleming ; R. PebodySource :
English descriptors
- mix :
- DNA Time Factors Treatment Outcome Vaccination/statistics & numerical data, H1N1 Subtype/classification/genetics/immunology/*isolation & purification Influenza A Virus, H3N2 Subtype/classification/genetics/immunology/*isolation & purification Influenza B virus/genetics/*immunology/isolation & purification Influenza Vaccines/*administration & dosage/immunology/therapeutic use Influenza, Human/*epidemiology/immunology/*prevention & control/virology Male Middle Aged Primary Health Care Reverse Transcriptase Polymerase Chain Reaction Seasons *Sentinel Surveillance Sequence Analysis, Adolescent Adult Aged Case-Control Studies Child Female Great Britain/epidemiology Hemagglutination Inhibition Tests Humans Influenza A Virus.
Abstract
The effectiveness of the 2012/13 trivalent seasonal influenza vaccine (TIV) was assessed using a test-negative case-control study of patients consulting primary care with influenza-like illness in the United Kingdom. Strain characterisation was undertaken on selected isolates. Vaccine effectiveness (VE) against confirmed influenza A(H3N2), A(H1N1) and B virus infection, adjusted for age, sex, surveillance scheme (i.e. setting) and month of sample collection was 26% (95% confidence interval (CI): -4 to 48), 73% (95% CI: 37 to 89) and 51% (95% CI: 34 to 63) respectively. There was an indication, although not significant, that VE declined by time since vaccination for influenza A(H3N2) (VE 50% within three months, 2% after three months, p=0.25). For influenza A(H3N2) this is the second season of low VE, contributing to the World Health Organization (WHO) recommendation that the 2013/14 influenza vaccine strain composition be changed to an A(H3N2) virus antigenically like cell-propagated prototype 2012/13 vaccine strain (A/Victoria/361/2011). The lower VE seen for type B is consistent with antigenic drift away from the 2012/13 vaccine strain. The majority of influenza B viruses analysed belong to the genetic clade 2 and were antigenically distinguishable from the 2012/13 vaccine virus B/Wisconsin/1/2010 clade 3. These findings supported the change to the WHO recommended influenza B vaccine component for 2013/14.
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Hal:hal-01262537Le document en format XML
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<front><div type="abstract" xml:lang="en"> <p>The effectiveness of the 2012/13 trivalent seasonal influenza vaccine (TIV) was assessed using a test-negative case-control study of patients consulting primary care with influenza-like illness in the United Kingdom. Strain characterisation was undertaken on selected isolates. Vaccine effectiveness (VE) against confirmed influenza A(H3N2), A(H1N1) and B virus infection, adjusted for age, sex, surveillance scheme (i.e. setting) and month of sample collection was 26% (95% confidence interval (CI): -4 to 48), 73% (95% CI: 37 to 89) and 51% (95% CI: 34 to 63) respectively. There was an indication, although not significant, that VE declined by time since vaccination for influenza A(H3N2) (VE 50% within three months, 2% after three months, p=0.25). For influenza A(H3N2) this is the second season of low VE, contributing to the World Health Organization (WHO) recommendation that the 2013/14 influenza vaccine strain composition be changed to an A(H3N2) virus antigenically like cell-propagated prototype 2012/13 vaccine strain (A/Victoria/361/2011). The lower VE seen for type B is consistent with antigenic drift away from the 2012/13 vaccine strain. The majority of influenza B viruses analysed belong to the genetic clade 2 and were antigenically distinguishable from the 2012/13 vaccine virus B/Wisconsin/1/2010 clade 3. These findings supported the change to the WHO recommended influenza B vaccine component for 2013/14.</p>
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