000132944 001__ 132944 000132944 005__ 20240229105041.0 000132944 0247_ $$2doi$$a10.1007/s11940-018-0498-1 000132944 0247_ $$2pmid$$apmid:29594595 000132944 0247_ $$2ISSN$$a1092-8480 000132944 0247_ $$2ISSN$$a1534-3138 000132944 0247_ $$2altmetric$$aaltmetric:35023365 000132944 037__ $$aDKFZ-2018-00583 000132944 041__ $$aeng 000132944 082__ $$a610 000132944 1001_ $$0P:(DE-He78)5ef8651b0f857b9c640aa5b1498c43b5$$aPlatten, Michael$$b0$$eFirst author$$udkfz 000132944 245__ $$aVaccine Strategies in Gliomas. 000132944 260__ $$aPhiladelphia, Pa.$$bCurrent Science Inc.$$c2018 000132944 3367_ $$2DRIVER$$aarticle 000132944 3367_ $$2DataCite$$aOutput Types/Journal article 000132944 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article$$bjournal$$mjournal$$s1660118080_9237$$xReview Article 000132944 3367_ $$2BibTeX$$aARTICLE 000132944 3367_ $$2ORCID$$aJOURNAL_ARTICLE 000132944 3367_ $$00$$2EndNote$$aJournal Article 000132944 520__ $$aTo discuss the current state of glioma vaccine development and highlight the challenges associated with clinical implementation of these approaches.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. 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