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牛分枝杆菌三种抗原(MPB70、19,000分子量蛋白和MPB57)的牛T细胞表位鉴定

Identification of bovine T-cell epitopes for three Mycobacterium bovis antigens: MPB70, 19,000 MW and MPB57.

作者信息

Pollock J M, Douglas A J, Mackie D P, Neill S D

机构信息

Department of Agriculture for Northern Ireland, Veterinary Sciences Division, Stormont, Belfast.

出版信息

Immunology. 1994 May;82(1):9-15.

Abstract

Bovine tuberculosis remains a serious problem in several regions, partly due to a lack of specific diagnostic tests. The aim of this study was to identify bovine T-cell epitopes for defined Mycobacterium bovis antigens using an experimental model of the natural disease. Panels of synthetic peptides (16-mers with five residue overlaps) were produced from published amino acid sequences for MPB70, the 19,000 MW antigen and MPB57. In vitro lymphocyte proliferation assays were used to identify T-cell epitopes. Lymphocytes from experimentally infected cattle proliferated in response to five epitopes (residues 88-105 and 144-163 for MPB70; 1-16 and 67-84 for the 19,000 MW antigen; and 85-100 for MBP57). These epitopes were not recognized by control, non-infected animals, but were recognized by field reactors to intradermal tuberculin testing. All five epitopes were recognized by three different breeds of cattle (Friesian, Charolais and Simmental). In addition, the bovine T-cell epitopes identified for the 19,000 MW antigen in this study were similar to epitopes previously reported for man and mouse. Thus, as well as identifying candidate reagents for improved diagnostic tests and vaccination, this study provides evidence for genetic promiscuity T-cell recognition of major myobacterial epitopes.

摘要

牛结核病在几个地区仍然是一个严重问题,部分原因是缺乏特异性诊断测试。本研究的目的是使用自然疾病的实验模型来鉴定针对特定牛分枝杆菌抗原的牛T细胞表位。从已发表的MPB70、19000MW抗原和MPB57的氨基酸序列制备了合成肽库(16聚体,有五个残基重叠)。体外淋巴细胞增殖试验用于鉴定T细胞表位。来自实验感染牛的淋巴细胞对五个表位有增殖反应(MPB70的第88 - 105位和144 - 163位;19000MW抗原的第1 - 16位和67 - 84位;以及MBP57的第85 - 100位)。这些表位未被对照的未感染动物识别,但被皮内结核菌素试验的现场反应动物识别。所有五个表位都被三种不同品种的牛(弗里斯兰牛、夏洛来牛和西门塔尔牛)识别。此外,本研究中为19000MW抗原鉴定的牛T细胞表位与先前报道的人和小鼠的表位相似。因此,除了鉴定用于改进诊断测试和疫苗接种的候选试剂外,本研究还为主要分枝杆菌表位的T细胞识别的遗传混杂性提供了证据。

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