Technical University of Denmark, National Veterinary Institute, Lindholm, DK-4771 Kalvehave, Denmark.
Vaccine. 2012 Oct 5;30(45):6376-81. doi: 10.1016/j.vaccine.2012.08.035. Epub 2012 Aug 30.
Marker vaccines offer the possibility to differentiate classical swine fever (CSF) infected from CSF vaccinated animals based on serology and their implementation will ensure free trade with pigs. Therefore, new generations of promising marker vaccines have been developed, among them the chimeric vaccine CP7_E2alf. However, in populations previously vaccinated with live attenuated vaccines like the C-strain, passive immunity through maternal antibodies can interfere with efficacy of CP7_E2alf vaccination. Therefore, the efficacy of CP7_E2alf was examined in piglets from sows vaccinated once intramuscularly with C-strain vaccine 4 weeks before farrowing. Thus, these piglets were vaccinated intramuscularly with CP7_E2alf at the age of 5 or 8 weeks. Subsequently, the piglets and their mock-vaccinated littermate controls were challenged 2 weeks post vaccination with highly virulent Classical swine fever virus (CSFV) strain "Koslov". CP7_E2alf provided clinical protection upon challenge as no severe clinical signs or mortality was observed in the vaccinated piglets. Post mortem examination revealed pathological changes associated to CSFV only in the mock-vaccinated piglets. No infectious CSFV could be isolated from the tonsils of the vaccinated piglets. Two weeks after vaccination at the time of challenge, the vaccinated piglets only, had an increase in the ELISA antibody titer. Interestingly, the maternally derived immunity in the mock-vaccinated control piglets seems to neutralize the challenge virus. Thus, the previously observed 100% mortality in naïve (negative for antibodies to CSFV) piglets infected with CSFV Koslov was reduced in the control piglets of this study to 30% for challenge at the age of 7 weeks and 50% at the age of 10 weeks, respectively. In conclusion, CP7_E2alf proved to be effective in preventing mortality, severe clinical signs and pathological lesions in 5 or 8 weeks old piglets positive for maternal antibodies derived from sows vaccinated intramuscularly 4 weeks before farrowing with one dose of C-strain vaccine.
标记疫苗提供了一种可能性,可以基于血清学将经典猪瘟(CSF)感染动物与 CSF 接种动物区分开来,其实施将确保与猪的自由贸易。因此,已经开发了新一代有前途的标记疫苗,其中包括嵌合疫苗 CP7_E2alf。然而,在先前用活减毒疫苗(如 C 株)接种的人群中,通过母源抗体产生的被动免疫可能会干扰 CP7_E2alf 疫苗的效力。因此,在母猪在分娩前 4 周通过肌肉内接种 C 株疫苗一次的情况下,检查了 CP7_E2alf 在仔猪中的效力。因此,这些仔猪在 5 或 8 周龄时通过肌肉内接种 CP7_E2alf 进行疫苗接种。随后,在疫苗接种后 2 周,用高致病性经典猪瘟病毒(CSFV)毒株“Koslov”对仔猪及其模拟疫苗接种的同窝对照进行攻毒。CP7_E2alf 在攻毒时提供了临床保护,因为未观察到接种仔猪出现严重的临床症状或死亡。剖检发现,仅在模拟疫苗接种的仔猪中存在与 CSFV 相关的病理变化。未从接种仔猪的扁桃体中分离到传染性 CSFV。在攻毒时的疫苗接种后 2 周,仅接种仔猪的 ELISA 抗体滴度增加。有趣的是,在模拟疫苗接种的对照仔猪中,母源免疫似乎中和了攻毒病毒。因此,在先前的研究中,在感染 CSFV Koslov 的无经验(对 CSFV 抗体呈阴性)仔猪中观察到的 100%死亡率在本研究的对照仔猪中分别降低到 7 周龄时的 30%和 10 周龄时的 50%。总之,CP7_E2alf 被证明在预防母源抗体阳性的 5 或 8 周龄仔猪的死亡率、严重的临床症状和病理损伤方面是有效的,这些仔猪来自于母猪在分娩前 4 周通过肌肉内接种 C 株疫苗一次的母猪。