2010
DOI: 10.1016/j.vaccine.2010.04.075
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Clinical evaluation to determine the appropriate paediatric formulation of a tick-borne encephalitis vaccine

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Cited by 23 publications
(24 citation statements)
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“…13,15 Here we present the evaluation of antibody persistence between the second and third doses of the primary vaccination course (6 mo after the first vaccination with either FSME-IMMUN ® Junior or Encepur ® Children) as well as the immunogenicity and safety following the third vaccination (administered approximately one year after the first vaccination) with FSME-IMMUN ® Junior. All subjects received the vaccine intramuscularly into the musculus deltoideus of the upper arm or-depending on the developmental and nutritional status of the child-into the musculus vastus lateralis of the upper leg.…”
Section: Methodsmentioning
confidence: 99%
“…13,15 Here we present the evaluation of antibody persistence between the second and third doses of the primary vaccination course (6 mo after the first vaccination with either FSME-IMMUN ® Junior or Encepur ® Children) as well as the immunogenicity and safety following the third vaccination (administered approximately one year after the first vaccination) with FSME-IMMUN ® Junior. All subjects received the vaccine intramuscularly into the musculus deltoideus of the upper arm or-depending on the developmental and nutritional status of the child-into the musculus vastus lateralis of the upper leg.…”
Section: Methodsmentioning
confidence: 99%
“…Several explanations for this observation have been suggested before [9,18] and include intrinsic differences in the vaccine formulations such as in the antigenic content and/or the excipients added. Ultimately, regardless of their relative differences in immune response, it is well established that both Encepur ® and FSME-IMMUN ® elicit effective immune responses against TBE after a complete primary vaccination series in adults and children [9,11,17,19,20], even if used interchangeably [9,18]. What has not been well established, however, is the duration of antibody persistence following primary immunization with these vaccines.…”
Section: Discussionmentioning
confidence: 99%
“…More extensive clinical data are available for inactivated, whole-virus vaccines to prevent diseases caused by flaviviruses, which structurally resemble alphaviruses, such as tick-borne encephalitis virus (TBEV), Japanese encephalitis virus, and yellow fever virus (21)(22)(23). The most extensively studied flavivirus vaccine is an alumadjuvanted inactivated whole-virus TBEV vaccine, which has been demonstrated to be safe and immunogenic in a multitude of clinical studies (24)(25)(26)(27)(28)(29)(30) and which has been used in Europe for several decades. In field studies, it has been demonstrated that three immunizations with a 2.4-g dose of the inactivated wholevirus TBEV vaccine provide approximately 99% effectiveness in preventing tick-borne encephalitis (22).…”
Section: Discussionmentioning
confidence: 99%