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Glioblastoma vaccines: past, present, and opportunities.
Xiong, Zujian; Raphael, Itay; Olin, Michael; Okada, Hideho; Li, Xuejun; Kohanbash, Gary.
Afiliação
  • Xiong Z; Department of Neurological Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA 15201, USA; Xiangya School of Medicine, Central South University, Changsha, Hunan 410008, PR China.
  • Raphael I; Department of Neurological Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA 15201, USA.
  • Olin M; Department of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA.
  • Okada H; Department of Neurological Surgery, University of California, San Francisco, CA 94143, USA.
  • Li X; Department of Neurosurgery, Xiangya Hospital, Central South University, Changsha, Hunan 410008, PR China; Hunan International Scientific and Technological Cooperation Base of Brain Tumor Research, Xiangya Hospital, Central South University, Changsha, Hunan 410008 PR China. Electronic address: lxjneu
  • Kohanbash G; Department of Neurological Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA 15201, USA; Department of Immunology, University of Pittsburgh, Pittsburgh, PA 15213, USA. Electronic address: gary.kohanbash@pitt.edu.
EBioMedicine ; 100: 104963, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38183840
ABSTRACT
Glioblastoma (GBM) is one of the most lethal central nervous systems (CNS) tumours in adults. As supplements to standard of care (SOC), various immunotherapies improve the therapeutic effect in other cancers. Among them, tumour vaccines can serve as complementary monotherapy or boost the clinical efficacy with other immunotherapies, such as immune checkpoint blockade (ICB) and chimeric antigen receptor T cells (CAR-T) therapy. Previous studies in GBM therapeutic vaccines have suggested that few neoantigens could be targeted in GBM due to low mutation burden, and single-peptide therapeutic vaccination had limited efficacy in tumour control as monotherapy. Combining diverse antigens, including neoantigens, tumour-associated antigens (TAAs), and pathogen-derived antigens, and optimizing vaccine design or vaccination strategy may help with clinical efficacy improvement. In this review, we discussed current GBM therapeutic vaccine platforms, evaluated and potential antigenic targets, current challenges, and perspective opportunities for efficacy improvement.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Glioblastoma / Vacinas Anticâncer Limite: Adult / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Glioblastoma / Vacinas Anticâncer Limite: Adult / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article