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MPT63衍生的HLA-A*0201限制性CD8+ T细胞表位对活动性肺结核的诊断潜力

The diagnostic potential of MPT63-derived HLA-A*0201-restricted CD8+ T-cell epitopes for active pulmonary tuberculosis.

作者信息

Duan Zhiliang, Li Dezhou, Jia Qingjun, Xu Juanjuan, Chen Xinyu, Xu Zhigang, Liu Huifang, Chen Bokun, Wen Jinsheng

机构信息

Department of Clinical Laboratory, Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Xueyuan West Road.

Institute of Arboviruses, School of Basic Medical Sciences, Wenzhou Medical University, Chashan, Wenzhou 325000.

出版信息

Microbiol Immunol. 2015 Dec;59(12):705-15. doi: 10.1111/1348-0421.12339.

Abstract

MPT63 protein is found only in Mycobacterium tuberculosis complex, including M. tuberculosis and M. bovis. Detection of MPT63-specific IFN-γ-secreting T cells could be useful for the diagnosis of tuberculosis (TB) diseases. In the present study, the HLA-A0201 restriction of ten predicted MPT63-derived CD8(+) T-cell epitopes was assessed on the basis of T2 cell line and HLA-A0201 transgenic mice. The diagnostic potential of immunogenic peptides in active pulmonary TB patients was evaluated using an IFN-γ enzyme-linked immunospot assay. It was found that five peptides bound to HLA-A0201 with high affinity, whereas the remaining peptides exhibited low affinity for HLA-A0201. Five immunogenic peptides (MPT6318-26 , MPT6329-37 , MPT6320-28 , MPT635-14 and MPT6310-19 ) elicited large numbers of cytotoxic IFN-γ-secreting T cells in HLA-A0201 transgenic mice. Each of the five immunogenic peptides was recognized by peripheral blood mononuclear cells from 45% to 73% of 40 HLA-A0201 positive TB patients. The total diagnostic sensitivity of the five immunogenic peptides was higher than that of a T-SPOT.TB assay (based on ESAT-6 and CFP-10) (93% versus 90%). It is noticeable that the diagnostic sensitivity of the combination of five immunogenic peptides and T-SPOT.TB assay reached 100%. These MPT63-derived HLA-A*0201-restricted CD8(+) T-cell epitopes would likely contribute to the immunological diagnosis of M. tuberculosis infection and may provide the components for designing an effective TB vaccine.

摘要

MPT63蛋白仅在结核分枝杆菌复合群中发现,包括结核分枝杆菌和牛分枝杆菌。检测MPT63特异性分泌γ干扰素的T细胞可能有助于结核病(TB)的诊断。在本研究中,基于T2细胞系和HLA-A0201转基因小鼠评估了10个预测的MPT63衍生的CD8(+) T细胞表位的HLA-A0201限制性。使用γ干扰素酶联免疫斑点试验评估免疫原性肽在活动性肺结核患者中的诊断潜力。发现5种肽与HLA-A0201具有高亲和力结合,而其余肽对HLA-A0201表现出低亲和力。5种免疫原性肽(MPT6318-26、MPT6329-37、MPT6320-28、MPT635-14和MPT6310-19)在HLA-A0201转基因小鼠中引发大量分泌细胞毒性γ干扰素的T细胞。40名HLA-A0201阳性结核病患者中,45%至73%的外周血单个核细胞识别这5种免疫原性肽中的每一种。这5种免疫原性肽的总诊断敏感性高于T-SPOT.TB检测(基于ESAT-6和CFP-10)(93%对90%)。值得注意的是,5种免疫原性肽与T-SPOT.TB检测联合使用时诊断敏感性达到100%。这些MPT63衍生的HLA-A*0201限制性CD8(+) T细胞表位可能有助于结核分枝杆菌感染的免疫学诊断,并可能为设计有效的结核病疫苗提供成分。

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