Department of Microbiology,National Veterinary Institute,SE-751 89 Uppsala,Sweden.
Department of Animal Science,Aarhus University,Blichers Allé 20, P.O. box 50, DK-8830, Tjele,Denmark.
Parasitology. 2019 Apr;146(5):625-633. doi: 10.1017/S0031182018001877. Epub 2018 Nov 9.
This study aimed to set up methodology to monitor parasite-specific T-cell activation in vitro using Eimeria tenella-infected chickens. A sonicated E. tenella sporozoite protein preparation was used for the activation of chicken spleen cell cultures. Proliferation assessed by 3H-thymidin incorporation or blast transformation of T-cells assessed by immunofluorescence labelling and flow cytometry were used as read-outs for activation. Results showed that E. tenella-specific proliferation was detected in cultures of spleen cells collected in a 'window' between 8 and 14 days after primary infection. However, due to high variation in proliferative responses between individuals and to high background proliferation, large numbers of observations were needed to obtain significant results. Moreover, the outcome was not improved by increasing the infection dose to chickens or by depletion of T-cell receptor (TCR) γ/δ expressing cells from cultures. An E. tenella-specific blast transformation response was observed for TCRα/β expressing cells within the same 'window', confirming the identity of the responding cells as classic T-cells. Thus, it is possible to study the kinetics of E. tenella-specific T-cell responses in vitro. However, more in-depth phenotypic identification of the responding T-cells could improve the methodology.
本研究旨在建立一种方法,利用感染柔嫩艾美耳球虫(Eimeria tenella)的鸡体外监测寄生虫特异性 T 细胞的激活。用超声处理的柔嫩艾美耳球虫裂殖子蛋白制剂激活鸡脾细胞培养物。通过 3H-胸腺嘧啶掺入或通过免疫荧光标记和流式细胞术评估的 T 细胞的细胞分裂转化来评估增殖,作为激活的读出。结果表明,在初次感染后 8 至 14 天的“窗口期”收集的脾细胞培养物中检测到柔嫩艾美耳球虫特异性增殖。然而,由于个体间增殖反应的高度变异性和高背景增殖,需要大量观察才能获得显著结果。此外,增加鸡的感染剂量或从培养物中耗尽 T 细胞受体(TCR)γ/δ表达细胞并不能改善结果。在同一“窗口期”内观察到 TCRα/β表达细胞的柔嫩艾美耳球虫特异性细胞分裂转化反应,证实了反应细胞作为经典 T 细胞的身份。因此,有可能在体外研究柔嫩艾美耳球虫特异性 T 细胞反应的动力学。然而,更深入地表征反应 T 细胞的表型可以改进该方法。