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Immune Escape in Glioblastoma: Mechanisms of Action and Implications for Immune Checkpoint Inhibitors and CAR T-Cell Therapy.
Yu, Catherine; Hsieh, Kristin; Cherry, Daniel R; Nehlsen, Anthony D; Resende Salgado, Lucas; Lazarev, Stanislav; Sindhu, Kunal K.
Afiliação
  • Yu C; Department of Radiation Oncology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
  • Hsieh K; Department of Radiation Oncology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
  • Cherry DR; Department of Radiation Oncology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
  • Nehlsen AD; Department of Radiation Oncology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
  • Resende Salgado L; Department of Radiation Oncology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
  • Lazarev S; Department of Radiation Oncology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
  • Sindhu KK; Department of Radiation Oncology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Biology (Basel) ; 12(12)2023 Dec 15.
Article em En | MEDLINE | ID: mdl-38132354
ABSTRACT
Glioblastoma, the most common primary brain cancer in adults, is characterized by a poor prognosis and resistance to standard treatments. The advent of immunotherapy has revolutionized the treatment of several cancers in recent years but has failed to demonstrate benefit in patients with glioblastoma. Understanding the mechanisms by which glioblastoma exerts tumor-mediated immune suppression in both the tumor microenvironment and the systemic immune landscape is a critical step towards developing effective immunotherapeutic strategies. In this review, we discuss the current understanding of immune escape mechanisms in glioblastoma that compromise the efficacy of immunotherapies, with an emphasis on immune checkpoint inhibitors and chimeric antigen receptor T-cell therapy. In parallel, we review data from preclinical studies that have identified additional therapeutic targets that may enhance overall treatment efficacy in glioblastoma when administered alongside existing immunotherapies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Biology (Basel) Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Biology (Basel) Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Suíça