Department of Animal Health and Bioscience, Faculty of Agricultural Sciences, Aarhus University, Tjele, Denmark.
Scand J Immunol. 2011 Jul;74(1):23-30. doi: 10.1111/j.1365-3083.2011.02534.x.
In this study, we have described the establishment of an antigen-specific T cell proliferation assay based on recall stimulation with Newcastle disease (ND) antigen; further, we have described the results obtained after recall stimulation of animals containing different major histocompatibility complex (MHC) haplotypes, vaccinated against ND. First optimization of the assay was performed to lower unspecific proliferation and to enhance antigen-specific T cell proliferation. These two issues were achieved using ethylene diamine tetra acetic acid as stabilizing agent in blood samples and autologous immune serum in culture medium. The optimized assay was used to screen chickens with different MHC haplotypes for their ability to perform T cell proliferation. Results showed that the antigen-specific response of CD4(+) and CD8(+) T cells from B12 chickens was generally low, whereas B13, B130 and B201 chickens were medium in CD4(+) or CD8(+) T cell responses. High responses were seen only in few animals of each haplotype and not in general. A polymorphism in the chicken CD8α gene was found in our experimental chicken lines, resulting in incapability to detect CD8α(+) T cells using antibodies from the CT8 clone. Screening chickens with alternative antibodies showed that antibodies from the 2-398 clone were able to discriminate all CD8α(+) cells from CD8α(-) cells, and consequently this antibody was used in a second vaccination experiment performed with chickens of the haplotypes B13 and B130. This experiment showed a significant difference in antigen-specific proliferation of CD4(+) T cells between the two lines, but not in CD8α(+) T cell proliferation.
在这项研究中,我们描述了一种基于新城疫(ND)抗原回忆刺激的抗原特异性 T 细胞增殖测定法的建立;此外,我们还描述了对含有不同主要组织相容性复合体(MHC)单倍型的、针对 ND 进行疫苗接种的动物进行回忆刺激后获得的结果。首先,我们对测定法进行了优化,以降低非特异性增殖并增强抗原特异性 T 细胞增殖。这两个问题是通过在血液样本中使用乙二胺四乙酸作为稳定剂和在培养基中使用自体免疫血清来实现的。优化后的测定法用于筛选具有不同 MHC 单倍型的鸡,以检测其 T 细胞增殖能力。结果表明,B12 鸡的 CD4(+)和 CD8(+)T 细胞的抗原特异性反应通常较低,而 B13、B130 和 B201 鸡的 CD4(+)或 CD8(+)T 细胞反应则处于中等水平。只有在每个单倍型的少数动物中才会看到高反应,而不是普遍存在。在我们的实验鸡系中发现了鸡 CD8α 基因的多态性,导致无法使用 CT8 克隆的抗体检测 CD8α(+)T 细胞。用替代抗体筛选鸡表明,来自 2-398 克隆的抗体能够区分 CD8α(+)细胞和 CD8α(-)细胞,因此该抗体用于对 B13 和 B130 单倍型的鸡进行的第二次疫苗接种实验。该实验显示了两种单倍型的鸡之间 CD4(+)T 细胞的抗原特异性增殖存在显著差异,但 CD8α(+)T 细胞增殖没有差异。