How flu vaccines work. Universal Influenza Vaccination of Children - the UK experience. 2 parts to an infection.. Direct effects.

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Bristol Children s Vaccine Centre Universal Influenza Vaccination of Children - the UK experience @adamhfinn DIPS, Korsør 9 th November 018 How flu vaccines work Specific (on target) direct effects indirect effects prevention of onward transmission Also downstream leading to off target effects Direct effects parts to an infection.. Antigen B The victim gets the infection usually from another person (but sometimes from their own flora, the environment or a non-human host) The victim passes the infection on to one or several* other victims. Antibody * = epidemic New cases Indirect effects R>1 R<1 Infections require there to be enough susceptibles in the population to be able to spread Direct Vaccines as tools to protect vulnerable individuals against infectious diseases Indirect Vaccines as tools to protect whole populations against infectious diseases Time 1

Flu Infectiousness Grandparenticide Flu England 017-18 Young child Virus in secretions Onset illness Adult 1 3 5 Days Flu why the fuss? Weekly ILI consultation rates across UK countries, 016-17 England Wales Significant annual epidemics with morbidity and resources usage especially in the young and the elderly and mortality in the elderly Scotland Northern Ireland Risk of global pandemics and related Armageddon scenarios See @cambridgewg 50 00 RSV 150 Ro ta 100 Flu 50 All 3 0-50 Immunise high risk groups, including pregnant women Stop them getting sick and dying 6 8 10 *Recommended but not Funded Old idea direct protection Immunise the elderly 0 Europe universal flu Recommendations for kids Austria IIV 7m to 15y RbnF* Finland 6m-3y IIV & LAIV funded Latvia IIV 6m-y funded Malta IIV 6m-5y RbnF Poland IIV 13m-19y RbnF Slovakia IIV 6m-1y funded Slovenia IIV 6m-y RbnF UK y-9y LAIV funded (age to school Y5) LAIV in Germany Sweden Norway http://vaccine-schedule.ecdc.europa.eu/pages/scheduler.aspx

New idea indirect protection Immunise children universally directly protect them Block transmission of flu Protect not only those at high risk but also much larger low risk group of all ages, children and adults Reichert et al NEJM 001 Cluster randomised study New vaccine - LAIV Isolated Hutterite communities in Canada 950 children aged 3-15y in 50 communities Randomised to TIV or HepA vaccines 300 unimmunised people studied for flu 3.1% of unimmunised people in immunised communities got PCR+ flu vs 7.6% in unimmunised communities (61% effective) Nasal spray high acceptability Efficacious in young children (but only licensed for >y) Loeb et al 010 JAMA Efficacy of LAIV Relative to Placebo Second Hutterite Cluster randomised study 3 season study 01-15 1186 children aged 36m-15y in 5 communities Randomised to IIV (7%) or LAIV (77%) vaccines (both trivalent) Children & 35 unimmunised people studied for flu A&B (PCR) 5.3% of people in LAIV immunised communities got PCR+ flu vs 5.% in IIV immunised communities (Hazard ratio 1.03 (0.85-1.)) 17 Ambrose et al., Vaccine, 30:886-89, 01. Loeb et al 016 Annals Internal Medicine 3

England/UK universal LAIV 013-1 Introduced for year olds changed to -3 year olds (1 dose each). Primary school children (5-10 yo in pilot areas) 01-15 - year olds 1 dose. More pilots including secondary schools (11+) 015-16-17-7 year olds. 017-18 -9 year olds School pilot schemes 01-15 England 01-15 (year ) Large seasonal epidemic Mostly H3N then B Both significantly drifted from vaccine strains Pebody et al. Eurosurveillance Oct 015 GP diagnosed ILI Excess respiratory mortality Primary Secondary None Primary Secondary None Pebody et al. Eurosurveillance Oct 015 Pebody et al. Eurosurveillance Oct 015 016-017 LAIV effectiveness Weekly ILI consultation rates across UK countries, 016-17 England -y 38.% 5-7y 55.% Scotland -y 59% 5-11y 73% Wales -3y 5.3% -7y 66.9% Northern Ireland -y 5.6% -7y 78.3%

H1N1pdm09 1.-1.6 Source: Wikipedia page Basic Reproduction Number Flu England 017-18 Features of 17-18 UK epidemic Predominantly H3N and B H3N in all flu vaccines worked relatively poorly thought to be due to in vitro antigenic drift apart in humans versus in egg culture B in trivalent vaccines Victoria so mismatched H1N1 in LAIV worked well effectiveness case-control studies 5