REVIEW article

Front. Oncol.

Sec. Molecular and Cellular Oncology

Volume 15 - 2025 | doi: 10.3389/fonc.2025.1613332

Vaccine Therapies for Glioma: clinical frontiers and potential breakthrough

Provisionally accepted
Ying  XingYing Xing1Caixia  LiuCaixia Liu1Yunfeng  FengYunfeng Feng2Shangyu  LiShangyu Li1Yuping  ChenYuping Chen1*
  • 1Baoding Hospital, Beijing Children’s Hospital, Capital Medical University, Baoding, China
  • 2Celest Therapeutics (Shanghai) Co., Ltd., Shanghai city, China

The final, formatted version of the article will be published soon.

Abstract: Glioma, the most common primary malignant brain tumor, is characterized by high recurrence and mortality rates. Its effective treatment remains a therapeutic challenge in clinical neuro-oncology. Despite over twenty years of exploring new therapies for glioma, progress in improving patient survival outcomes has been limited. Tumor vaccines, as a promising therapeutic approach, may offer hope for glioma treatment. Currently, tumor vaccines targeting glioma include peptide vaccines, dendritic cell vaccines, and nucleic acid vaccines. Neoantigens, due to their high specificity and resistance to central immune tolerance, are ideal targets for tumor vaccines. Although promising results have been resulted in preclinical and clinical for glioma vaccines, there are still challenges impeding vaccine therapy for glioma. Therefore, future glioma vaccine applications must focus on the important roles of epitope spreading and antigen quality in enhancing immune response and therapeutic effectiveness. In this review, we discuss the current glioma vaccine antigen targets and types, introduce recent important clinical studies on glioma vaccines, and propose strategies to address potential barriers to vaccine application.

Keywords: Glioma, Vaccine, Epitope spreading, neoantigen, antigen hierarchy sequencing

Received: 17 Apr 2025; Accepted: 09 Jun 2025.

Copyright: © 2025 Xing, Liu, Feng, Li and Chen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Yuping Chen, Baoding Hospital, Beijing Children’s Hospital, Capital Medical University, Baoding, China

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