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Vaccine Strategies in Gliomas

机译:Gliomas疫苗策略

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摘要

Abstract Purpose of review To discuss the current state of glioma vaccine development and highlight the challenges associated with clinical implementation of these approaches. Recent findings Vaccination strategies against gliomas have matured considerably during the past years, although proof-of efficacy from controlled clinical trials is still lacking. Advances in antigen discovery, including the definition of neoepitopes including epidermal growth factor receptor variant III (EGFRvIII), isocitrate dehydrogenase (IDH)1R132H and Histone (H)3.3K27M, using multi-omic approaches and computational algorithms allow targeting single antigens, but also implementing truly personalized approaches. In addition, new concepts of vaccine manufacturing including RNA and DNA vaccines improve immunogenicity and applicability in personalized settings. Summary As an increasing amount of clinical data defy the concept of the central nervous system (CNS) as a strictly immunoprivileged site, novel vaccine approaches enter the clinic including critical efforts to identify biomarkers of response and resistance and strategies to overcome the immunosuppressive glioma microenvironment.
机译:摘要审查目的探讨胶质瘤疫苗开发当前状态,突出与这些方法临床实施相关的挑战。然而,过去几年,对胶质瘤的疫苗接种策略已经成熟,尽管来自受控临床试验的验证效果仍然缺乏。抗原发现的进展,包括新内膜术的定义,包括表皮生长因子受体变体III(EGFRVIII),异柠檬酸脱氢酶(IDH)1R132H和组蛋白(H)3.3k27m,使用多环境方法和计算算法允许靶向单一抗原,但也是实施真正个性化方法。此外,包括RNA和DNA疫苗的疫苗制造的新概念可提高个性化环境中的免疫原性和适用性。总结作为临床数据的增加,临床数据缺乏中枢神经系统(CNS)的概念作为严格免疫蓬恼的现场,新的疫苗方法进入诊所,包括识别抗反症和抗性的生物标志物的重要努力,以克服免疫抑制胶质瘤微环境。

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