Department of Veterinary Medicine, Federal Rural University of Pernambuco, Recife, Brazil.
Department of Virology and Experimental Therapy, Aggeu Magalhães Research Center, Recife, Brazil.
Open Vet J. 2024 Apr;14(4):1019-1028. doi: 10.5455/OVJ.2024.v14.i4.9. Epub 2024 Apr 30.
Canine distemper (CD) is a worldwide spread disease that has been described in 12 families of mammals, especially in the Carnivora order, being better studied in domestic canines where vaccination represents the best means of control. CD is controlled by vaccination, but many cases of the disease still occur in vaccinated animals.
The aim of this work was to study antigen-specific epitopes that can subsidize the development of a new vaccine approach.
Mapping of T cell reactive epitopes for CD virus (CDV) was carried out through enzyme-linked immunospot assays using 119 overlapped synthetic peptides from the viral hemagglutinin protein, grouped in 22 pools forming a matrix to test the immune response of 32 animals.
Evaluations using the criteria established to identify reactive pools, demonstrated that 26 animals presented at least one reactive pool, that one pool was not reactive to any animal, and six pools were the most frequent among the reactive peptides. The crisscrossing of the most reactive pools in the matrix revealed nine peptides considered potential candidate epitopes for T cell stimulation against the CDV and those were used to design an protein, containing also predicted epitopes for B cell stimulation, and further analyzed using immune epitope databases to ensure protein quality and stability.
The final optimized protein presents characteristics that qualify it to be used to develop a new prototype epitope-based anti-CDV vaccine.
犬瘟热(CD)是一种在全球范围内传播的疾病,已在 12 个哺乳动物科中被描述,尤其是在食肉目动物中,在犬科动物中研究得更为深入,疫苗接种是控制该疾病的最佳手段。CD 通过疫苗接种来控制,但在接种疫苗的动物中仍有许多病例发生。
本研究旨在研究抗原特异性表位,以辅助开发新型疫苗方法。
使用酶联免疫斑点法(ELISPOT),通过 119 个重叠的犬瘟热病毒(CDV)血凝蛋白合成肽进行 T 细胞反应性表位的作图,这些肽分为 22 个池,形成一个矩阵,以测试 32 只动物的免疫反应。
使用既定标准评估反应性池,结果显示 26 只动物至少有一个反应性池,一个池对任何动物均无反应,六个池是反应性肽中最常见的。矩阵中最反应性的池的交叉揭示了九个被认为是针对 CDV 的 T 细胞刺激的潜在候选表位肽,这些肽用于设计一种含有预测的 B 细胞刺激表位的蛋白质,并进一步使用免疫表位数据库进行分析,以确保蛋白质的质量和稳定性。
最终优化的蛋白质具有可用于开发新型基于表位的抗 CDV 疫苗的特征。