Kariuki T M, Grootenhuis J G, Dolan T T, Bishop R P, Baldwin C L
International Laboratory for Research on Animal Diseases, Nairobi, Kenya.
Infect Immun. 1990 Nov;58(11):3574-81. doi: 10.1128/iai.58.11.3574-3581.1990.
Immunity to infection by the protozoan parasite Theileria parva in cattle is partially attributable to cytotoxic T cells, which kill lymphocytes infected with the schizont stage of the parasite. Here we evaluated five stocks of buffalo-derived T. parva lawrencei parasites and two stocks of cattle-derived T. parva parva parasites for their ability to induce in vivo cytotoxic T cells which can kill lymphocytes infected with a wide variety of strains of T. parva parasites. A group of seven full-sibling cattle, produced by embryo transfer and matched for at least one major histocompatibility complex class I haplotype, were immunized by infection and treatment with the parasite stocks. Target cells used in in vitro cytotoxicity assays were infected with five buffalo-derived parasite stocks and five cattle-derived parasite stocks, including T. parva parva and T. parva bovis. Immunization with any of the seven parasite stocks resulted in the generation of cytotoxic T cells which recognized parasite antigens on most if not all of the target cell lines tested, although the T. parva bovis stock was the least effective at doing so. Further in-depth analyses performed with peripheral blood mononuclear cells from one of the cattle immunized with T. parva lawrencei parasites showed that the pattern of killing of the panel of target cells was altered when either cells infected with different parasite stocks or clones of infected cells were used as stimulator cells in vitro, suggesting the presence of more than one population of parasite-specific cytotoxic effector cells in the peripheral blood mononuclear cells. However, clones of these cytotoxic effector cells recognized common or cross-reactive antigen epitopes expressed by the entire panel of infected target cells. These T-cell clones will be useful for identifying common T-cell antigen epitopes of T. parva and the parasite genes encoding them.
牛对原生动物寄生虫小泰勒虫感染的免疫力部分归因于细胞毒性T细胞,这些细胞毒性T细胞可杀死被该寄生虫裂殖体阶段感染的淋巴细胞。在此,我们评估了五株源自水牛的小泰勒虫劳伦斯亚种寄生虫和两株源自牛的小泰勒虫小亚种寄生虫诱导体内细胞毒性T细胞的能力,这些细胞毒性T细胞能够杀死被多种小泰勒虫寄生虫菌株感染的淋巴细胞。通过胚胎移植产生了一组七头全同胞牛,它们至少匹配一种主要组织相容性复合体I类单倍型,并通过感染和用寄生虫株进行处理来进行免疫。体外细胞毒性试验中使用的靶细胞被五株源自水牛的寄生虫株和五株源自牛的寄生虫株感染,包括小泰勒虫小亚种和小泰勒虫牛亚种。用这七种寄生虫株中的任何一种进行免疫都会导致细胞毒性T细胞的产生,这些细胞毒性T细胞能识别大多数(如果不是全部)测试靶细胞系上的寄生虫抗原,尽管小泰勒虫牛亚种株在这方面效果最差。对用小泰勒虫劳伦斯亚种寄生虫免疫的其中一头牛的外周血单个核细胞进行的进一步深入分析表明,当用感染不同寄生虫株的细胞或感染细胞的克隆作为体外刺激细胞时,靶细胞杀伤模式会发生改变,这表明外周血单个核细胞中存在不止一种寄生虫特异性细胞毒性效应细胞群体。然而,这些细胞毒性效应细胞的克隆识别整个感染靶细胞系所表达的共同或交叉反应性抗原表位。这些T细胞克隆将有助于鉴定小泰勒虫的共同T细胞抗原表位以及编码它们的寄生虫基因。