2008
DOI: 10.1016/j.vaccine.2008.04.034
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Foot-and-mouth disease vaccine potency testing in cattle using homologous and heterologous challenge strains: Precision of the “Protection against Podal Generalisation” test

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Cited by 37 publications
(37 citation statements)
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“…It has been reported that this indirect potency measurement is at least as precise as the in vivo challenge test, and can be standardized to 'antigen PD 50 ' values [31]. Development of such an assay system need to be done in the country in order to avoid animal ethics problem, biosecurity and biosafety concerns, and problem in the disposal of infected cattle when challenge method is used for potency testing of the vaccine.…”
Section: Vaccine and Vaccinationmentioning
confidence: 99%
“…It has been reported that this indirect potency measurement is at least as precise as the in vivo challenge test, and can be standardized to 'antigen PD 50 ' values [31]. Development of such an assay system need to be done in the country in order to avoid animal ethics problem, biosecurity and biosafety concerns, and problem in the disposal of infected cattle when challenge method is used for potency testing of the vaccine.…”
Section: Vaccine and Vaccinationmentioning
confidence: 99%
“…Vaccine efficacy as well as surveillance of vaccine immunity is performed by serology. Strain-specific antibody titers obtained with liquid phase blocking ELISA (LPBE) have been statistically correlated to in vivo protection to assess vaccine potency and herd immunity through the estimation of a percentage of expected protection (EPP) [8][9][10][11][12].…”
Section: Introductionmentioning
confidence: 99%
“…However, many studies have discussed alternative FMD vaccine potency tests that are amenable from an animal welfare perspective and show better statistical reliability (1,2,9,23). In this regard, the RP ELISA could be employed as a simple and reliable assay to replace the LPB ELISA or the VNT.…”
mentioning
confidence: 99%