Next-generation antigen-presenting cell immune therapeutics for gliomas

Catalina Lee-Chang*, Maciej S. Lesniak*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

25 Scopus citations

Abstract

Antigen presentation machinery and professional antigen-presenting cells (APCs) are fundamental for an efficacious immune response against cancers, especially in the context of T cell–centric immunotherapy. Dendritic cells (DCs), the gold standard APCs, play a crucial role in initiating and maintaining a productive antigen-specific adaptive immunity. In recent decades, ex vivo–differentiated DCs from circulating CD14+ monocytes have become the reference for APC-based immunotherapy. DCs loaded with tumor-associated antigens, synthetic peptides, or RNA activate T cells with antitumor properties. This strategy has paved the way for the development of alternative antigen-presenting vaccination strategies, such as monocytes, B cells, and artificial APCs, that have shown effective therapeutic outcomes in preclinical cancer models. The search for alternative APC platforms was initiated by the overall limited clinical impact of DC vaccines, especially in indications such as gliomas, a primary brain tumor known for resistance to any immune intervention. In this Review, we navigate the APC immune therapeutics’ past, present, and future in the context of primary brain tumors.

Original languageEnglish (US)
Article numbere163449
JournalJournal of Clinical Investigation
Volume133
Issue number3
DOIs
StatePublished - Feb 1 2023

Funding

The authors are supported by the National Cancer Institute (R37CA258426 to CLC; R35CA197725 and P50CA221747 to MSL), the National Institute of Neurological Disorders and Stroke (R01NS115955 to MSL), the Cancer Research Institute, the Malnati Brain Tumor Institute, and the American Brain Tumor Association.

ASJC Scopus subject areas

  • General Medicine

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