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一种能够激活T淋巴细胞的特异性结核分枝杆菌蛋白的鉴定。

Identification of a specific Mycobacterium tuberculosis protein able to activate T lymphocytes.

作者信息

Vismara D, Favaro M, Mariani F, Piccolella E, Colizzi V

机构信息

Dipartimento di Biologia, Università degli Studi Tor Vergata, Rome, Italy.

出版信息

Ann Ist Super Sanita. 1991;27(1):21-6.

PMID:1720294
Abstract

The recent advances in the field of immunology and molecular biology allow to consider not distant the identification of protective antigens to be used in new prophilactic and diagnostic tools. In our laboratory we have analysed a M. tuberculosis expression library by murine monoclonal antibodies, human sera and human T lymphocytes. We have identified a 35 Kd protein present only on the M. tuberculosis complex (M. tuberculosis, M. bovis, M. africanum). This 35 Kd protein is also detected, by immunohistological analysis, inside the alveolar macrophage of pulmonary tuberculosis patients. Both recombinant beta-galactosidase and MS2 polymerase-fused proteins have been produced and used to perform western blotting and T cell proliferation assay. As the cloned fragment contains an internal EcoRI restriction site, it was possible to identify two fragments of 1.7 and 2.2 kb respectively. Southern blot analysis showed that both the fragments hibridized with the genomic DNA from M. tuberculosis complex but not with the DNA from other mycobacterial isolates from 12 pulmonary tuberculous patients hibridized with the 1.7 kb fragment. The possible use of this insert for the molecular diagnosis of tuberculosis is under investigation.

摘要

免疫学和分子生物学领域的最新进展使得在不久的将来有望鉴定出可用于新型预防和诊断工具的保护性抗原。在我们实验室,我们利用鼠单克隆抗体、人血清和人T淋巴细胞分析了结核分枝杆菌表达文库。我们鉴定出一种仅存在于结核分枝杆菌复合群(结核分枝杆菌、牛分枝杆菌、非洲分枝杆菌)中的35 Kd蛋白。通过免疫组织学分析,在肺结核患者的肺泡巨噬细胞内也检测到了这种35 Kd蛋白。已经制备了重组β-半乳糖苷酶和MS2聚合酶融合蛋白,并用于进行蛋白质印迹和T细胞增殖试验。由于克隆片段含有一个内部EcoRI限制性酶切位点,因此有可能分别鉴定出1.7 kb和2.2 kb的两个片段。Southern印迹分析表明,这两个片段均与结核分枝杆菌复合群的基因组DNA杂交,但不与来自12例肺结核患者的其他分枝杆菌分离株的DNA杂交,其中有部分患者的DNA与1.7 kb片段杂交。该插入片段在结核病分子诊断中的潜在用途正在研究中。

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