Appendix 20
Recommendations for tests for induction of antibodies to NSP antigens by FMD vaccines Extract from source: EMEA/CVMP/775/02-FINAL. Committee for Medicinal Products for Veterinary Use (CVMP) Position Paper on Requirements for Vaccines against Foot-And-Mouth Disease Position Paper adopted by CVMP on 16 June 2004, with date of coming into effect of 16 December 2004. http://www.emea.eu.int
Quality requirements in support of information related to non-structural proteins Manufacturers should supply data to substantiate information provided on the Summary of Product Characteristics (SPC) that a vaccine does not induce antibody to one or more NS proteins. To support such information: (i) The manufacturing process should include one or more steps to purify the virus from cellular or other contaminants, including NS proteins that are produced during virus growth in cell culture. As part of the authorisation dossier, the manufacturer should present data from immunochemical tests such as SDS-PAGE, irnmunoblotting, or some form of competitive based assay to demonstrate that the purification process reduces the level of NS proteins in the final purified, concentrated antigen. However, it is unlikely that any purification process can completely remove NS proteins and there is currently no method of predicting the immunogenicity of any proteins remaining. Therefore demonstrating that the vaccine does not induce significant levels of NS antibody in immunised animals currently represents the only means of supporting information on the SPC relating to NS antibody. (ii) The manufacturer should conduct a test to demonstrate that repeated immunisation of one or more of the indicated species with vaccines formulated to contain the maximum permitted amount and number of antigens does not result in seroconversion to NS proteins. Such a test should be required to be conducted at least once for each FMD vaccine (as defined above) for which information is provided (i.e the information relates to the formulation of both adjuvants and antigens together and not to the antigens alone). In order to reduce the use of animals, it may be possible to conduct this test in the animals used for demonstrating the safety of the administration of a single dose, an overdose and a repeat dose in Part III of the application dossier. A recommended immunisation and testing program is as follows: Prior to Day 0: Collect a sample of blood from a minimum of 10 animals to verify freedom from antibody to FMD virus structural and non-structural proteins. The animals should have no history of exposure to FMD, should not have been previously vaccinated and should be free of non-specific antibody to FMD virus NS antibodies. Day 0: Administer to a single site a minimum of two doses of a vaccine containing the maximum permitted amount of antigen of each of the maximum permitted number of antigens (i.e. if the authorisation permits up to 1 5ug of up to four different antigens then the vaccine should contain at least I 5ug of each of at least four different antigens) Day 14-28: Administer a second, identical injection after the interval recommended in the basic vaccination schedule, usually two to four weeks Day 42 onwards: Administer a third, identical injection between a minimum of one and a maximum of six months after the second injection. Day 56 onwards: Collect serum samples between two and four weeks after the last vaccination and test for antibody to NS proteins. The antibody levels against specified NS proteins should be lower than those considered as positive in a validated test. (iii) Manufacturers may use alternative immunisations and testing schedules provided that they can justify that the schedule used is the most likely to induce an antibody response to NS proteins. (iv)The manufacturer should use a test that has been adequately validated and, where possible, one that has been recognised by an international organisation such as Office International des Epizooties (OlE). In the absence of internationally recognised standards for NS antibody serology, the manufacturer should justify the validation performed to the satisfaction of the competent authority by reference to published data, by independent validation of the test by an internationally recognised FMD reference laboratory and/or by conducting suitable ‘in-house’ validation studies.
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