Wang Zejing, Storb Rainer, Tapscott Stephen J, Riddell Stanley
Program in Transplantation Biology, Division of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Methods Mol Biol. 2012;792:65-74. doi: 10.1007/978-1-61779-325-7_5.
Adeno-associated viral (AAV) vector-mediated gene transfer represents a promising gene replacement strategy for treating various genetic diseases. One obstacle in using viral-derived vectors for in vivo gene delivery is the development of host immune responses to the vector. Recent studies have demonstrated cellular immune responses specific to capsid proteins of various AAV serotypes in animal models and in human trials for different diseases. We developed a canine-specific ELISPOT assay to detect such immunity in dogs received AAV treatment. Here, we describe in detail the use of a constructed panel of overlapping peptides spanning the entire VP1 sequence of AAV capsid protein to detect specific T-cell responses in peripheral blood in dogs following intramuscular injection of AAV. This high-throughput method allows the identification of T-cell epitopes without the need for large cell numbers and the need for major histocompatibility complex molecule-matched cell lines.
腺相关病毒(AAV)载体介导的基因转移是治疗各种遗传疾病的一种有前景的基因替代策略。使用病毒衍生载体进行体内基因递送的一个障碍是宿主对载体产生免疫反应。最近的研究已经在动物模型和针对不同疾病的人体试验中证明了针对各种AAV血清型衣壳蛋白的细胞免疫反应。我们开发了一种犬特异性ELISPOT检测方法,以检测接受AAV治疗的犬的这种免疫反应。在此,我们详细描述了使用一组构建的覆盖AAV衣壳蛋白整个VP1序列的重叠肽来检测犬肌肉注射AAV后外周血中的特异性T细胞反应。这种高通量方法无需大量细胞,也无需主要组织相容性复合体分子匹配的细胞系即可鉴定T细胞表位。