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Human glioblastoma stem-like cells are more sensitive to allogeneic NK and T cell-mediated killing compared with serum-cultured glioblastoma cells

机译:与血清培养的胶质母细胞瘤细胞相比,人胶质母细胞瘤干样细胞对同种异体NK和T细胞介导的杀伤更为敏感

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摘要

Glioblastoma multiforme (GBM) is the most dramatic primary brain cancer with a very poor prognosis because of inevitable disease recurrence. The median overall survival is less than 1 year after diagnosis. Cancer stem cells have recently been disclosed in GBM. GBM stem-like cells (GSCs) exhibit resistance to radio/chemotherapeutic treatments and are therefore considered to play an important role in disease recurrence. GSCs are thus appealing targets for new treatments for GBM patients. In this study, we show that GBM cells with stem cell characteristics are resistant to lysis mediated by resting natural killer (NK) cells because of the expression of MHC class I molecules. However, GSCs are killed by lectin-activated NK cells. Furthermore, in experiments using the therapeutic antibody CetuximAb, we show that GSCs are sensitive to antibody-mediated cytotoxicity. We confirm the sensitivity of GSC to cytotoxicity carried out by IL2-activated NK cells and tumor-specific T cells. More importantly, we show that GSCs are more sensitive to NK and T cell-mediated lysis relatively to their corresponding serum-cultured GBM cells obtained from the same initial tumor specimen. Altogether, these results demonstrate the sensitivity of GSC to immune cell cytotoxicity and, therefore, strongly suggest that GSCs are suitable target cells for immunotherapy of GBM patients.
机译:多形性胶质母细胞瘤(GBM)是最剧烈的原发性脑癌,由于不可避免的疾病复发,因此预后很差。诊断后中位总生存期少于1年。癌症干细胞最近已在GBM中公开。 GBM干样细胞(GSC)表现出对放射/化学疗法治疗的抵抗力,因此被认为在疾病复发中起重要作用。因此,GSC是GBM患者新治疗的目标。在这项研究中,我们表明具有干细胞特征的GBM细胞由于MHC I类分子的表达而对静止的自然杀伤(NK)细胞介导的裂解具有抗性。但是,GSC被凝集素激活的NK细胞杀死。此外,在使用治疗性抗体CetuximAb的实验中,我们显示GSC对抗体介导的细胞毒性敏感。我们确认GSC对由IL2激活的NK细胞和肿瘤特异性T细胞进行的细胞毒性的敏感性。更重要的是,我们显示,相对于从相同初始肿瘤标本中获得的相应血清培养的GBM细胞,GSC对NK和T细胞介导的裂解更为敏感。总而言之,这些结果证明了GSC对免疫细胞毒性的敏感性,因此强烈暗示GSC是GBM患者免疫疗法的合适靶细胞。

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