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口服狂犬病病毒疫苗株SPBN GASGAS在狐狸中的长期免疫原性和效力

Long-Term Immunogenicity and Efficacy of the Oral Rabies Virus Vaccine Strain SPBN GASGAS in Foxes.

作者信息

Freuling Conrad M, Kamp Verena Te, Klein Antonia, Günther Maria, Zaeck Luca, Potratz Madlin, Eggerbauer Elisa, Bobe Katharina, Kaiser Christian, Kretzschmar Antje, Ortmann Steffen, Schuster Peter, Vos Adriaan, Finke Stefan, Müller Thomas

机构信息

Institute of Molecular Virology and Cell Biology, Friedrich-Loeffler-Institut (FLI), WHO Collaborating Centre for Rabies Surveillance and Research, OIE Reference Laboratory for Rabies, 17493 Greifswald-Insel Riems, Germany.

IDT Biologika GmbH, 06861 Dessau-Rosslau, Germany.

出版信息

Viruses. 2019 Aug 27;11(9):790. doi: 10.3390/v11090790.

Abstract

To evaluate the long-term immunogenicity of the live-attenuated, oral rabies vaccine SPBN GASGAS in a full good clinical practice (GCP) compliant study, forty-six (46) healthy, seronegative red foxes () were allocated to two treatment groups: group 1 ( = 31) received a vaccine bait containing 1.7 ml of the vaccine of minimum potency (10 FFU/mL) and group 2 ( = 15) received a placebo-bait. In total, 29 animals of group 1 and 14 animals of group 2 were challenged at 12 months post-vaccination with a fox rabies virus isolate (10 MICLD/mL). While 90% of the animals offered a vaccine bait resisted the challenge, only one animal (7%) of the controls survived. All animals that had seroconverted following vaccination survived the challenge infection at 12 months post-vaccination. Rabies specific antibodies could be detected as early as 14 days post-vaccination. Based on the kinetics of the antibody response to SPBN GASGAS as measured in ELISA and RFFIT, the animals maintained stable antibody titres during the 12-month pre-challenge observation period at a high level. The results indicate that successful vaccination using the oral route with this new rabies virus vaccine strain confers long-term duration of immunity beyond one year, meeting the same requirements as for licensure as laid down by the European Pharmacopoeia.

摘要

为在一项完全符合良好临床实践(GCP)的研究中评估减毒口服狂犬病疫苗SPBN GASGAS的长期免疫原性,将46只健康、血清阴性的赤狐分配到两个治疗组:第1组(n = 31)接受含有1.7毫升最低效力(10 FFU/mL)疫苗的疫苗诱饵,第2组(n = 15)接受安慰剂诱饵。总共,第1组的29只动物和第组的14只动物在接种疫苗后12个月用一种狐狸狂犬病病毒分离株(10 MICLD/mL)进行攻毒。虽然90%接受疫苗诱饵的动物抵抗了攻毒,但对照组只有一只动物(7%)存活。所有接种疫苗后血清阳转的动物在接种疫苗后12个月的攻毒感染中存活下来。狂犬病特异性抗体最早可在接种疫苗后14天检测到。根据ELISA和RFFIT检测到的对SPBN GASGAS抗体反应的动力学,动物在攻毒前12个月的观察期内保持高水平的稳定抗体滴度。结果表明,使用这种新型狂犬病病毒疫苗株通过口服途径成功接种可提供超过一年的长期免疫持续时间,符合欧洲药典规定的许可要求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0bf/6784248/26a224a1aa30/viruses-11-00790-g001.jpg

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