首页> 外文期刊>Scandinavian journal of immunology. >HLA-A*0201-restricted cytotoxic T-cell epitopes in three PE/PPE family proteins of Mycobacterium tuberculosis.
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HLA-A*0201-restricted cytotoxic T-cell epitopes in three PE/PPE family proteins of Mycobacterium tuberculosis.

机译:HLA-A * 0201限制了结核分枝杆菌的三种PE / PPE家族蛋白中的细胞毒性T细胞表位。

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摘要

CD8+ T cells are thought to play an important role in protective immunity against tuberculosis. We report the identification of three peptides derived from Rv1818c, Rv3812 and Rv3018c proteins of Mycobacterium tuberculosis that bound to HLA-A*0201 molecules and their ability to induce in vitro T-cell response in peripheral blood lymphocytes from HLA-A*0201-positive healthy individuals (PPD+) and patients with TB. The peptide-specific cytotoxic T lymphocytes (CTL) generated were capable of recognizing peptide pulsed targets. Three 9-mer peptides bound with high affinity to HLA-A*0201 and displayed low dissociation rates of the bound peptide from HLA. Epitope-specific recognition was demonstrated by the release of perforin and gamma-interferon. Overall, our results demonstrate the presence of HLA class I-restricted CD8+ CTL against proteins from PE and PPE proteins of M. tuberculosis and identify epitopes that are strongly recognized by HLA-A*0201-restricted CD8+ T cells in humans. These epitopes thus represent potential subunit components for the design of vaccines against tuberculosis.
机译:人们认为CD8 + T细胞在抵抗结核病的保护性免疫中起着重要作用。我们报告鉴定了与结核分枝杆菌的Rv1818c,Rv3812和Rv3018c蛋白结合到HLA-A * 0201分子的三种肽的鉴定,以及它们在从HLA-A * 0201阳性的外周血淋巴细胞中诱导体外T细胞反应的能力健康个体(PPD +)和结核病患者。产生的肽特异性细胞毒性T淋巴细胞(CTL)能够识别肽脉冲靶标。三个与HLA-A * 0201高亲和力结合的9-mer肽,显示结合的肽与HLA的解离速率低。穿孔素和γ-干扰素的释放证明了表位特异性识别。总体而言,我们的结果证明存在针对人类结核分枝杆菌PE和PPE蛋白的HLA I类限制性CD8 + CTL,并鉴定了人类中HLA-A * 0201限制性CD8 + T细胞强烈识别的表位。因此,这些表位代表用于设计抗结核疫苗的潜在亚基成分。

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