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Editor, Senior Moderator
Vaccine
Available online 17 August 2012
In Press, Uncorrected Proof ? Note to users
Cover image
Dose sparing intradermal trivalent influenza (2010/2011) vaccination overcomes reduced immunogenicity of the 2009 H1N1 strain
Ivan F.N. Hunga, b, Corresponding author contact information, E-mail the corresponding author,
Yotam Levinc,
Kelvin K.W. Toa,
Kwok-Hung Chana,
Anna Jinxia Zhanga,
Patrick Lia,
Clara Lia,
Ting Xua,
Tin-Yan Wonga,
Kwok-Yung Yuena
a State Key Laboratory for Emerging Infectious Diseases, Carol Yu's Centre for Infection and Division of Infectious Diseases, The University of Hong Kong, Queen Mary Hospital, Hong Kong Special Administrative Region
b Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong Special Administrative Region
c NanoPass Technologies Ltd., Israel
Received 2 January 2012. Revised 5 August 2012. Accepted 8 August 2012. Available online 17 August 2012.
http://dx.doi.org/10.1016/j.vaccine.2012.08.014, How to Cite or Link Using DOI
Background
We hypothesized that low dose intradermal vaccination of the trivalent influenza vaccine (TIV) delivered by the MicronJet600? (NanoPass Technologies, Israel) would be non-inferior to the full dose intramuscular and mid dose Intanza? vaccination in the elderly and the chronically ill adults.
Methods
We performed a prospective randomized trial on elderly and chronically ill adults. Subjects were randomly assigned into 4 groups. Groups ID3 and ID9 received reduced dose ID TIV [3 μg and 9 μg of hemagglutinin (HA) per strain respectively) delivered by MicronJet600? (NanoPass Technologies, Israel). Group INT9 received reduced dose ID TIV (9 μg) delivered by Becton Dickinson's Soluvia? device (Intanza?9, Sanofi-Pasteur, France). Control group IM15 received a full dose IM TIV (15 μg). We measured antibody titers by hemagglutination inhibition (HAI) and microneutralization (MN) assays at baseline and day 21.
Results
Baseline characteristics for all groups were similar (group and sample sizes: ID3 = 63; ID9 = 68; INT9 = 65; and IM15 = 66). At day 21 post vaccination, the GMT ratio and the seroconversion rates difference for all three strains of the ID vaccine groups were non-inferior to the IM vaccine group. The seroconversion rate, seroprotection rate, and the GMT of the H1N1 strains by HAI and MN assays were significantly higher in the ID groups compared with the full dose IM vaccine group. The seroconversion rates of the H3N2 strain by HAI assay were also significantly higher in the ID groups when compared with the full dose IM group. Direct comparison among the three ID devices showed no significant differences. No serious adverse events related to vaccination were reported.
Conclusion
Dose-sparing ID TIV can overcome reduced immunogenicity of the H1N1 strain, and according to some measures, for the H3N2 strain. At risk subjects indicated for the TIV should be considered for intradermal immunization to compensate for reduced immunogenicity.
Highlights
► Reduced immunogenicity of the H1N1 component of the current TIV demonstrated. ► Reduced immunogenicity of the H1N1 component overcome by intradermal vaccination. ► Efficacy between two different intradermal devices compared. ► Superior efficacy of intradermal over conventional intramuscular vaccination demonstrated.
http://www.sciencedirect.com/science/article/pii/S0264410X12011930
Available online 17 August 2012
In Press, Uncorrected Proof ? Note to users
Cover image
Dose sparing intradermal trivalent influenza (2010/2011) vaccination overcomes reduced immunogenicity of the 2009 H1N1 strain
Ivan F.N. Hunga, b, Corresponding author contact information, E-mail the corresponding author,
Yotam Levinc,
Kelvin K.W. Toa,
Kwok-Hung Chana,
Anna Jinxia Zhanga,
Patrick Lia,
Clara Lia,
Ting Xua,
Tin-Yan Wonga,
Kwok-Yung Yuena
a State Key Laboratory for Emerging Infectious Diseases, Carol Yu's Centre for Infection and Division of Infectious Diseases, The University of Hong Kong, Queen Mary Hospital, Hong Kong Special Administrative Region
b Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong Special Administrative Region
c NanoPass Technologies Ltd., Israel
Received 2 January 2012. Revised 5 August 2012. Accepted 8 August 2012. Available online 17 August 2012.
http://dx.doi.org/10.1016/j.vaccine.2012.08.014, How to Cite or Link Using DOI
Background
We hypothesized that low dose intradermal vaccination of the trivalent influenza vaccine (TIV) delivered by the MicronJet600? (NanoPass Technologies, Israel) would be non-inferior to the full dose intramuscular and mid dose Intanza? vaccination in the elderly and the chronically ill adults.
Methods
We performed a prospective randomized trial on elderly and chronically ill adults. Subjects were randomly assigned into 4 groups. Groups ID3 and ID9 received reduced dose ID TIV [3 μg and 9 μg of hemagglutinin (HA) per strain respectively) delivered by MicronJet600? (NanoPass Technologies, Israel). Group INT9 received reduced dose ID TIV (9 μg) delivered by Becton Dickinson's Soluvia? device (Intanza?9, Sanofi-Pasteur, France). Control group IM15 received a full dose IM TIV (15 μg). We measured antibody titers by hemagglutination inhibition (HAI) and microneutralization (MN) assays at baseline and day 21.
Results
Baseline characteristics for all groups were similar (group and sample sizes: ID3 = 63; ID9 = 68; INT9 = 65; and IM15 = 66). At day 21 post vaccination, the GMT ratio and the seroconversion rates difference for all three strains of the ID vaccine groups were non-inferior to the IM vaccine group. The seroconversion rate, seroprotection rate, and the GMT of the H1N1 strains by HAI and MN assays were significantly higher in the ID groups compared with the full dose IM vaccine group. The seroconversion rates of the H3N2 strain by HAI assay were also significantly higher in the ID groups when compared with the full dose IM group. Direct comparison among the three ID devices showed no significant differences. No serious adverse events related to vaccination were reported.
Conclusion
Dose-sparing ID TIV can overcome reduced immunogenicity of the H1N1 strain, and according to some measures, for the H3N2 strain. At risk subjects indicated for the TIV should be considered for intradermal immunization to compensate for reduced immunogenicity.
Highlights
► Reduced immunogenicity of the H1N1 component of the current TIV demonstrated. ► Reduced immunogenicity of the H1N1 component overcome by intradermal vaccination. ► Efficacy between two different intradermal devices compared. ► Superior efficacy of intradermal over conventional intramuscular vaccination demonstrated.
http://www.sciencedirect.com/science/article/pii/S0264410X12011930