PROTAC 工程化蛋白/DNA 纳米抗原是癌症免疫治疗中树突状细胞疫苗的有效增强剂
PROTAC-Engineered Protein/DNA Nanoantigen is a Potent Booster for Dendritic Cell Vaccines in Cancer Immunotherapy.
树突状细胞(DC)疫苗在肿瘤免疫治疗中的疗效常因抗原交叉呈递(XPT)效率低下导致的免疫原性较弱而受到限制。
英文原题:Friend or Foe? Exploring the Role of Cytomegalovirus (HCMV) Infection in Head and Neck Tumors.
Friend or Foe? Exploring the Role of Cytomegalovirus (HCMV) Infection in Head and Neck Tumors.
尽管人巨细胞病毒(HCMV)不被视为致癌病原体,但它与多种恶性肿瘤相关。
尽管人巨细胞病毒(HCMV)不被视为致癌病原体,但它与多种恶性肿瘤相关。相反,多项研究报告了该病毒可能的抗肿瘤特性,显然是通过HCMV激发的T细胞肿瘤杀伤作用介导的;近期这些特性正在临床试验中通过树突状细胞疫苗和HCMV特异性细胞毒性T细胞用于抗癌治疗的研究。在本研究中,我们通过Spearman相关性分析、单因素和多因素回归分析,分析了全球73个国家头颈部肿瘤与HCMV感染之间的关系。有趣的是,HCMV在鼻咽癌患者中表现出促癌作用;相反,该病毒与唇/口腔区域肿瘤及唾液腺肿瘤呈反向关联(即抗肿瘤关联)。尽管这种推测的保护效应最初在甲状腺肿瘤和下咽部肿瘤中也有观察到,但经过多因素回归分析后,该关联未能成立。喉癌与HCMV感染之间无关联。看来,取决于组织类型,HCMV可能同时发挥保护性和致癌性作用。该病毒在全球范围内观察到的保护性特征可能在未来用于唾液腺肿瘤及唇/口腔区域肿瘤的治疗方法。由于相关性并不一定意味着因果关系,需要来自全面临床研究的更深入分子分析来证实我们的发现。
Although not regarded as an oncogenic pathogen, the human cytomegalovirus (HCMV) has been associated with a wide array of malignancies. Conversely, a number of studies report on possible anti-tumor properties of the virus, apparently mediated via HCMV-galvanized T-cell tumor killing; these were recently being investigated in clinical trials for the purposes of anti-cancer treatment by means of dendritic cell vaccines and HCMV-specific cytotoxic T cells. In the present study, we have analyzed the relation between a complement of head-and-neck tumors and HCMV infection across 73 countries worldwide using Spearman correlation, univariate and multivariate regression analysis. Intriguingly, HCMV was found to be pro-oncogenic in patients with nasopharyngeal carcinoma; contrarywise, the virus manifested an inverse (i.e., anti-tumor) association with the tumors of the lip/oral region and the salivary glands. Although this putative protective effect was noted initially for thyroid neoplasia and hypopharyngeal tumors as well, after multivariate regression analysis the connection did not hold. There was no association between laryngeal cancer and HCMV infection. It would appear that, depending on the tissue, HCMV may exert both protective and oncogenic effects. The globally observed protective feature of the virus could potentially be utilized in future therapeutic approaches for salivary tumors and neoplasia in the lip/oral region. As correlation does not necessarily imply causation, more in-depth molecular analyses from comprehensive clinical studies are warranted to substantiate our findings.
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