Background
In this study we compared the immunogenicity of influenza vaccine administered intradermally
to the standard intramuscular vaccination in lung transplant recipients.
Methods
Patients were randomized to receive the trivalent inactivated seasonal 2008–9 influenza
vaccine containing either 6 μg (intradermal) or 15 μg (intramuscular) of hemagglutinin
per viral strain. Immunogenicity was assessed by measurement of geometric mean titer
of antibodies using the hemagglutination-inhibition (HI) assay. Vaccine response was
defined as a 4-fold or higher increase of antibody titers to at least one vaccine
antigen.
Results
Eighty-five patients received either the intradermal (n = 41) or intramuscular (n = 44) vaccine. Vaccine response was seen in 6 of 41 patients (14.6%) in the intradermal
vs 8 of 43 (18.6%) in the intramuscular group (p = 0.77). Seroprotection (HI ≥1:32) was 39% for H1N1, 83% for H3N2 and 29% for B strain
in the intradermal group vs 28% for H1N1, 98% for H3N2 and 58% for B strain in the
intramuscular group (p = 0.36 for H1N1, p = 0.02 for H3N2, p < 0.01 for B). Mild adverse events were seen in 44% of patients in the intradermal
group and 34% in the intramuscular group (p = 0.38).
Conclusions
Immunogenicity of the 2008–9 influenza vaccine given intradermally or intramuscularly
was overall poor in lung transplant recipients. Novel strategies for influenza vaccination
in this population are needed.
Keywords
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Article info
Publication history
Published online: March 07, 2011
Identification
Copyright
© 2011 International Society for Heart and Lung Transplantation. Published by Elsevier Inc. All rights reserved.