Key result
Vaccination with a live attenuated HCLV C-strain vaccine in CSFV postnatally persistently infected pigs failed to induce any detectable humoral or cellular immune response or vaccine viral RNA replication.
Why the study?
Does the hog cholera lapinised virus vaccine (HCLV) induce an immune response in CSFV postnatally persistently infected pigs?
Does the hog cholera lapinised virus vaccine (HCLV) induce an immune response in CSFV postnatally persistently infected pigs?
This study demonstrates the absence of an immune response to vaccination in pigs persistently infected with classical swine fever virus.
Answers are grounded in this paper and cite their sources.
May explain persistent CSF despite vaccination; leaves open whether updated vaccines are required.
Classical swine fever (CSF) causes major losses in pig farming, with various degrees of disease severity. Efficient live attenuated vaccines against classical swine fever virus (CSFV) are used routinely in endemic countries. However, despite intensive vaccination programs in these areas for more than 20 years, CSF has not been eradicated. Molecular epidemiology studies in these regions suggests that the virus circulating in the field has evolved under the positive selection pressure exerted by the immune response to the vaccine, leading to new attenuated viral variants. Recent work by our group demonstrated that a high proportion of persistently infected piglets can be generated by early postnatal infection with low and moderately virulent CSFV strains. Here, we studied the immune response to a hog cholera lapinised virus vaccine (HCLV), C-strain, in six-week-old persistently infected pigs following post-natal infection. CSFV-negative pigs were vaccinated as controls. The humoral and interferon gamma responses as well as the CSFV RNA loads were monitored for 21 days post-vaccination. No vaccine viral RNA was detected in the serum samples and tonsils from CSFV postnatally persistently infected pigs for 21 days post-vaccination. Furthermore, no E2-specific antibody response or neutralising antibody titres were shown in CSFV persistently infected vaccinated animals. Likewise, no of IFN-gamma producing cell response against CSFV or PHA was observed. To our knowledge, this is the first report demonstrating the absence of a response to vaccination in CSFV persistently infected pigs.
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Muñoz‐González et al. (2015) studied Classical swine fever virus (CSFV) postnatal persistent infection (n=8). Hog cholera lapinised virus vaccine (HCLV), C-strain vs. Pestivirus-free vaccinated pigs was evaluated on Humoral and cellular immune response (E2-specific antibodies, neutralizing antibodies, IFN-gamma) and vaccine viral RNA detection. Vaccination with a live attenuated HCLV C-strain vaccine in CSFV postnatally persistently infected pigs failed to induce any detectable humoral or cellular immune response or vaccine viral RNA replication.
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