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一种35千道尔顿的蛋白质是人类针对麻风分枝杆菌免疫反应的主要靶点。

A 35-kilodalton protein is a major target of the human immune response to Mycobacterium leprae.

作者信息

Triccas J A, Roche P W, Winter N, Feng C G, Butlin C R, Britton W J

机构信息

Centenary Institute of Cancer Medicine and Cell Biology, Newtown, New South Wales, Australia.

出版信息

Infect Immun. 1996 Dec;64(12):5171-7. doi: 10.1128/iai.64.12.5171-5177.1996.

Abstract

The control of leprosy will be facilitated by the identification of major Mycobacterium leprae-specific antigens which mirror the immune response to the organism across the leprosy spectrum. We have investigated the host response to a 35-kDa protein of M. leprae. Recombinant 35-kDa protein purified from Mycobacterium smegmatis resembled the native antigen in the formation of multimeric complexes and binding by monoclonal antibodies and sera from leprosy patients. These properties were not shared by two forms of 35-kDa protein purified from Escherichia coli. The M. smegmatis-derived 35-kDa protein stimulated a gamma interferon-secreting T-cell proliferative response in the majority of paucibacillary leprosy patients and healthy contacts of leprosy patients tested. Cellular responses to the protein in patients with multibacillary leprosy were weak or absent, consistent with hyporesponsiveness to M. leprae characteristic of this form of the disease. Almost all leprosy patients and contacts recognized the 35-kDa protein by either a T-cell proliferative or an immunoglobulin G antibody response, whereas few tuberculosis patients recognized the antigen. This specificity was confirmed in guinea pigs, with the 35-kDa protein eliciting strong delayed-type hypersensitivity in M. leprae-sensitized animals but not in those sensitized with Mycobacterium tuberculosis or Mycobacterium bovis BCG. Therefore, the M. leprae 35-kDa protein appears to be a major and relatively specific target of the human immune response to M. leprae and is a potential component of a diagnostic test to detect exposure to leprosy or a vaccine to combat the disease.

摘要

鉴定主要的麻风分枝杆菌特异性抗原将有助于麻风病的控制,这些抗原能反映整个麻风病谱中机体对该病原体的免疫反应。我们研究了宿主对麻风分枝杆菌一种35 kDa蛋白的反应。从耻垢分枝杆菌中纯化的重组35 kDa蛋白在形成多聚体复合物以及与麻风病患者的单克隆抗体和血清结合方面类似于天然抗原。从大肠杆菌中纯化的两种形式的35 kDa蛋白不具有这些特性。在大多数检测的少菌型麻风病患者和麻风病患者的健康接触者中,耻垢分枝杆菌来源的35 kDa蛋白刺激了分泌γ干扰素的T细胞增殖反应。多菌型麻风病患者对该蛋白的细胞反应较弱或不存在,这与该型疾病对麻风分枝杆菌反应低下的特征一致。几乎所有麻风病患者及其接触者通过T细胞增殖反应或免疫球蛋白G抗体反应识别35 kDa蛋白,而很少有结核病患者识别该抗原。在豚鼠中证实了这种特异性,35 kDa蛋白在麻风分枝杆菌致敏的动物中引发强烈的迟发型超敏反应,但在结核分枝杆菌或牛分枝杆菌卡介苗致敏的动物中则不会。因此,麻风分枝杆菌35 kDa蛋白似乎是人类对麻风分枝杆菌免疫反应的主要且相对特异的靶点,并且是检测麻风病暴露的诊断试验或对抗该疾病疫苗的潜在组成部分。

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