Department of Preventive Veterinary Medicine, Shandong Agricultural University, 61 Daizong Street, Taian City, Shandong Province 271018, China; Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, Shandong Agricultural University, 61 Daizong Street, Taian City, Shandong Province 271018, China.
Department of Preventive Veterinary Medicine, Shandong Agricultural University, 61 Daizong Street, Taian City, Shandong Province 271018, China; Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, Shandong Agricultural University, 61 Daizong Street, Taian City, Shandong Province 271018, China.
Virus Res. 2015 Dec 2;210:62-8. doi: 10.1016/j.virusres.2015.06.024. Epub 2015 Jul 18.
The intricate sequence and antigenic variability of avian leukosis virus subgroup J (ALV-J) have led to unprecedented difficulties in the development of vaccines. Much experimental evidence demonstrates that ALV-J mutants have caused immune evasion and pose a challenge for traditional efforts to develop effective vaccines. To investigate the potential of a multi-epitope vaccination strategy to prevent chickens against ALV-J infections, a recombinant chimeric multi-epitope protein X (rCMEPX) containing both immunodominant B and T epitope concentrated domains selected from the major structural protein of ALV-J using bioinformatics approach was expressed in Escherichia coli Rosetta (DE3). Its immunogenicity and protective efficacy was studied in chickens. The results showed that rCMEPX could elicit neutralizing antibodies and cellular responses, and antibodies induced by rCMEPX could specifically recognize host cell naturally expressed ALV-J proteins, which indicated that the rCMEPX is a good immunogen. Challenge experiments showed 80% chickens that received rCMEPX were well protected against ALV-J challenge. This is the first report of a chimeric multi-epitope protein as a potential immunogen against ALV-J.
禽白血病病毒亚群 J(ALV-J)序列复杂且具有抗原变异性,这使得疫苗的开发面临前所未有的困难。大量实验证据表明,ALV-J 突变体已导致免疫逃逸,这对传统的开发有效疫苗的努力构成了挑战。为了研究多表位疫苗接种策略预防鸡感染 ALV-J 的潜力,使用生物信息学方法从 ALV-J 的主要结构蛋白中选择免疫显性 B 和 T 表位集中的区域,构建了包含这些表位的重组嵌合多表位蛋白 X(rCMEPX),并在大肠杆菌 Rosetta(DE3)中表达。在鸡中研究了其免疫原性和保护效力。结果表明,rCMEPX 能够引发中和抗体和细胞反应,并且 rCMEPX 诱导的抗体可以特异性识别宿主细胞中自然表达的 ALV-J 蛋白,这表明 rCMEPX 是一种良好的免疫原。攻毒实验表明,接受 rCMEPX 免疫的 80%的鸡能够很好地抵抗 ALV-J 攻毒。这是首例关于嵌合多表位蛋白作为针对 ALV-J 的潜在免疫原的报告。