2010
DOI: 10.1016/j.vaccine.2010.08.015
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Immunogenicity and safety of intradermal influenza vaccination in renal transplant patients who were non-responders to conventional influenza vaccination

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Cited by 55 publications
(41 citation statements)
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“…[21][22][23] In addition, 15 g of intradermal vaccine showed similar responses to intramuscular vaccine in a cohort of kidney transplant recipients who were non-responders to a previous intramuscular vaccine. 24 In contrast to studies performed in immunocompetent patients, we did not observe a higher rate of local adverse events in the intradermal group. This is in keeping with a previous study from our group using a boosting intradermal dose of influenza vaccine, where local reactions were seen in only 13% of lung transplant recipients.…”
Section: Discussioncontrasting
confidence: 99%
“…[21][22][23] In addition, 15 g of intradermal vaccine showed similar responses to intramuscular vaccine in a cohort of kidney transplant recipients who were non-responders to a previous intramuscular vaccine. 24 In contrast to studies performed in immunocompetent patients, we did not observe a higher rate of local adverse events in the intradermal group. This is in keeping with a previous study from our group using a boosting intradermal dose of influenza vaccine, where local reactions were seen in only 13% of lung transplant recipients.…”
Section: Discussioncontrasting
confidence: 99%
“…Recently, Morelon and colleagues have reported that intradermal inXuenza vaccination has an enhanced immunogenicity and probably leads to an increased protection against inXuenza in RT recipients who did not respond to conventional intramuscular vaccine application [34]. To prevent these vulnerable patients from inXuenza infection, annual inXuenza vaccination is strongly recommended in healthcare professionals and contact persons including young children who have often to be considered immunologically naïve [35].…”
Section: Discussionmentioning
confidence: 99%
“…[113][114][115] Nevertheless, in a study performed in chronic obstructive pulmonary disease patients, who received either 0.2 ml (6 μg of HA per virus strain) split into two site ID injections or a single 0.5 ml, full dose, IM injection, antibody responses of the ID arm were lower than those of IM group, even if each strain of the ID vaccination met the CHMP requirements. 116 In conclusion, based upon the reported clinical experience, ID vaccines need to be considered safe and immunogenic, being a valid alternative to other currently available products for the active immune-prevention of seasonal influenza in both adults and elderly individuals.…”
Section: O N O T D I S T R I B U T Ementioning
confidence: 99%