Brown W C, Zhao S, Rice-Ficht A C, Logan K S, Woods V M
Department of Veterinary Pathobiology, Texas A&M University, College Station 77843.
Infect Immun. 1992 Oct;60(10):4364-72. doi: 10.1128/iai.60.10.4364-4372.1992.
Helper T cell clones from two Babesia bovis-immune cattle were characterized for use in identification of potentially protective immunogens of B. bovis merozoites. Proliferation assays with 11 CD4+ clones revealed a differential pattern of response to soluble cytosolic antigen, membrane-enriched antigen, detergent extracts of the membrane-enriched antigen, soluble culture supernatant exoantigen, and different geographical isolates of B. bovis as well as Babesia bigemina parasites. When the data were combined, the clones could be grouped according to five different patterns of response. One group recognized only the membrane-enriched fraction of New World and Australian parasites. Four remaining groups recognized antigens found in the cytosolic as well as the membrane-enriched fraction, and clones representative of each group were used to identify cytosolic antigens fractionated by anion-exchange chromatography with the use of fast-performance liquid chromatography. One clone (C97.3C3), which responded to all B. bovis isolates and to B. bigemina, recognized a single peak of activity that eluted with 0.25 M NaCl and contained protein bands of 70 and 75 kDa. The remaining clones were stimulated by a second antigenic peak that eluted between 0.35 and 0.45 M NaCl and contained protein bands of 42, 47, 56, and 84 kDa. The majority of the clones produced interferon, whereas tumor necrosis factor alpha/tumor necrosis factor beta production was less frequent. These studies provide the basis for using helper T cell clones to identify potentially protective immunogens of B. bovis and delineate a minimum of five helper T cell epitopes recognized by two immune cattle.
对来自两头感染牛巴贝斯虫的免疫牛的辅助性T细胞克隆进行了表征,以用于鉴定牛巴贝斯虫裂殖子潜在的保护性免疫原。用11个CD4 +克隆进行的增殖试验显示,对可溶性胞质抗原、富含膜的抗原、富含膜的抗原的去污剂提取物、可溶性培养上清液外抗原、牛巴贝斯虫不同地理分离株以及双芽巴贝斯虫寄生虫的反应模式存在差异。当将数据合并时,这些克隆可根据五种不同的反应模式进行分组。一组仅识别新世界和澳大利亚寄生虫的富含膜的部分。其余四组识别在胞质以及富含膜的部分中发现的抗原,并使用每组的代表性克隆通过快速高效液相色谱法鉴定经阴离子交换色谱分离的胞质抗原。一个对所有牛巴贝斯虫分离株和双芽巴贝斯虫有反应的克隆(C97.3C3)识别出一个单一的活性峰,该峰在0.25 M NaCl处洗脱,包含70和75 kDa的蛋白条带。其余克隆受到在0.35至0.45 M NaCl之间洗脱的第二个抗原峰的刺激,该峰包含42、47、56和84 kDa的蛋白条带。大多数克隆产生干扰素,而肿瘤坏死因子α/肿瘤坏死因子β的产生频率较低。这些研究为使用辅助性T细胞克隆鉴定牛巴贝斯虫潜在的保护性免疫原提供了基础,并确定了至少五个被两头免疫牛识别的辅助性T细胞表位。