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表达针对结核分枝杆菌 38 kDa 抗原的 TCR 的基因工程 CD4+和 CD8+ T 细胞的开发。

Development of genetically engineered CD4+ and CD8+ T cells expressing TCRs specific for a M. tuberculosis 38-kDa antigen.

机构信息

Institute of Molecular Immunology, School of Biotechnology, Southern Medical University, Guangzhou 510515, China.

出版信息

J Mol Med (Berl). 2011 Sep;89(9):903-13. doi: 10.1007/s00109-011-0760-4. Epub 2011 May 10.

Abstract

Cell-mediated immunity is critical to the clearance of Mycobacterium tuberculosis due to the primarily intracellular niche of this pathogen. Adoptive transfer of M. tuberculosis-specific effector T cells has been shown to confer immunity to M. tuberculosis-infected recipients resulting in M. tuberculosis clearance. However, it is difficult to generate sufficient numbers of M. tuberculosis antigen-specific T cells in a short time. Recent studies have developed T cell receptor (TCR) gene-modified T cells that allow for the rapid generation of large numbers of antigen-specific T cells. Many TCRs that target various tumor and viral antigens have now been isolated and shown to have functional activity. Nevertheless, TCRs specific for intracellular bacterial antigens (including M. tuberculosis antigens) have yet to be isolated and their functionality confirmed. We isolated M. tuberculosis 38-kDa antigen-specific HLA class I and class II-restricted TCRs and modified the TCR gene C regions by substituting nine amino acids with their murine TCR homologs (minimal murinization). Results showed that both wild-type and minimal murinized TCR genes were successfully cloned into retroviral vectors and transduced into primary CD4(+) and CD8(+) T cells and displayed anti-M. tuberculosis activity. As expected, minimal murinized TCRs displayed higher cell surface expression levels and stronger anti-M. tuberculosis activity than wild-type TCRs. To the best of our knowledge, this is the first report describing TCRs targeting M. tuberculosis antigens and this investigation provides the basis for future TCR gene-based immunotherapies that can be designed for the treatment of immunocompromised M. tuberculosis-infected patients.

摘要

细胞介导的免疫对于清除结核分枝杆菌至关重要,因为这种病原体主要存在于细胞内。已经证明,结核分枝杆菌特异性效应 T 细胞的过继转移可以赋予结核分枝杆菌感染受者免疫力,导致结核分枝杆菌清除。然而,在短时间内产生足够数量的结核分枝杆菌抗原特异性 T 细胞是困难的。最近的研究已经开发了 T 细胞受体(TCR)基因修饰的 T 细胞,允许快速产生大量抗原特异性 T 细胞。现在已经分离出许多针对各种肿瘤和病毒抗原的 TCR,并证明它们具有功能活性。然而,针对细胞内细菌抗原(包括结核分枝杆菌抗原)的 TCR 尚未被分离出来,其功能也尚未得到证实。我们分离了结核分枝杆菌 38kDa 抗原特异性 HLA Ⅰ类和Ⅱ类限制性 TCR,并通过用其小鼠 TCR 同源物取代九个氨基酸来修饰 TCR 基因 C 区(最小化鼠源化)。结果表明,野生型和最小化鼠源化 TCR 基因都成功地克隆到逆转录病毒载体中,并转导到原代 CD4(+)和 CD8(+)T 细胞中,并显示出抗结核分枝杆菌活性。正如预期的那样,最小化鼠源化 TCR 比野生型 TCR 具有更高的细胞表面表达水平和更强的抗结核分枝杆菌活性。据我们所知,这是首次描述针对结核分枝杆菌抗原的 TCR 的报告,这项研究为未来基于 TCR 基因的免疫疗法提供了基础,可用于治疗免疫功能低下的结核分枝杆菌感染患者。

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