Influenza Vaccine With Topical Imiquimod in Influenza Vaccine Non-responsive Children

This study is a cross-over randomized-controlled trial (RCT). The outline of the study is shown in Figure 1. This study is divided into two parts: (i) screening for vaccine non-responders; and (ii) RCT for vaccine responsiveness using second dose IIV-IM, IIV-ID or IIV-Q-ID.

Children and adolescents between 8 and 18 years old will be recruited through our network of primary and secondary schools that have participated the Seasonal Influenza Vaccination School Outreach Programme before the influenza vaccination campaign. Information sheets, a consent form and a health demographics form indicating that they fulfill the inclusion and exclusion criteria (see below) will be distributed to the parents through the participating schools. A study hotline will be available for parents to contact the study team to answer any enquiries.

In the health demographics form, apart from questions related to the inclusion and exclusion criteria, the study team will also enquire about the subjects' demographics, including birth, gender, past medical history, and body weight and height. Previous influenza vaccination history will also be sought, including age at receiving the first influenza vaccine, whether the subjects have received influenza vaccines in the last season and the type of influenza vaccines they received.

All subjects should be receiving 0.5ml IM quadrivalent IIV, which contains 15micrograms hemagglutinin of each influenza strain, through the Seasonal Influenza Vaccination School Outreach Programme. Consented subjects will have 5-10ml clotted blood and 3ml EDTA blood draw at day 21 post-vaccination at school by our outreach study team. The parents of all participating subjects will receive an incentive equivalent to HKD 100. They will also receive their influenza vaccine response results in concealed envelops distributed through the schools.

Post-vaccination HAI titer against the Influenza B Yamagata strain ≤10 will be considered as "preliminary no seroconversion". The same serum taken on day 21 post-vaccination will be further processed to confirm that their HAI titer against the other Influenza A H1N1 and H3N2 and Influenza B Victoria strains are also ≤10. MN assay for all four strains will also be performed as the baseline for the part 2 RCT.

Non-responders will be called back to attend a research clinic and will be randomized to one of the following revaccination strategies: (i) repeat 0.5ml IM Quadrivalent IIV (IIV-IM) (15micrograms haemagglutinin per vaccine strain); (ii) 0.1ml ID Quadrivalent IIV (IIV-ID) (3micrograms haemagglutinin per vaccine strain); or (iii) 0.1ml ID Quadrivalent IIV (3micrograms haemagglutinin antigen per vaccine strain) + 5% imiquimod cream (IIV-Q-ID). Subjects randomized to receive 5% imiquimod cream will have the injection site disinfected by 70% alcohol swab followed by application of the imiquimod cream for 5 minutes before the intradermal injection over a 16cm2 skin area of the deltoid described in previous studies. 0.1ml IIV, which contains 3micrograms hemagglutinin of each influenza strain, will be administered intradermally using a MicronJetTM microneedle. All subjects will be observed for 15 to 30 minutes in the waiting area for any local adverse reactions. These subjects will be called back on day 7 and 21 after the second dose of vaccination for blood testing. 5- 10ml clotted blood will be obtained to measure the vaccine response. HAI and MN assays against the four vaccine strains will be performed.

To determine the association between HLA alleles and IIV non-responsiveness, HLA genotyping will be performed among non-responders and responders in 1:2 ratios. Assuming that there will be 72-100 IIV non-responders from our cohort, HLA genotyping will be performed in 200 age- and gender-matched IIV responder controls.