Synthetic High-density Lipoprotein Nanodiscs for Personalized Immunotherapy against Gliomas

Lindsay Scheetz, Padma Kadiyala, Xiaoqi Sun, Sejin Son, Alireza Hassani Najafabadi, Marisa Aikins, Pedro R. Lowenstein, Anna Schwendeman, Maria G. Castro, James J. Moon

Research output: Contribution to journalArticlepeer-review

52 Scopus citations

Abstract

Purpose: Gliomas are brain tumors with dismal prognoses. The standard-of-care treatments for gliomas include surgical resection, radiation, and temozolomide administration; however, they have been ineffective in providing significant increases in median survival. Antigen-specific cancer vaccines and immune checkpoint blockade may provide promising immunotherapeutic approaches for gliomas. Experimental Design: We have developed immunotherapy delivery vehicles based on synthetic high-density lipoprotein (sHDL) loaded with CpG, a Toll-like receptor-9 agonist, and tumor-specific neoantigens to target gliomas and elicit immune-mediated tumor regression. Results: We demonstrate that vaccination with neoantigen peptide-sHDL/CpG cocktail in combination with anti–PD-L1 immune checkpoint blocker elicits robust neoantigen-specific T-cell responses against GL261 cells and eliminated established orthotopic GL261 glioma in 33% of mice. Mice remained tumor free upon tumor cell rechallenge in the contralateral hemisphere, indicating the development of immunologic memory. Moreover, in a genetically engineered murine model of orthotopic mutant IDH1 (mIDH1) glioma, sHDL vaccination with mIDH1 neoantigen eliminated glioma in 30% of animals and significantly extended the animal survival, demonstrating the versatility of our approach in multiple glioma models. Conclusions: Overall, our strategy provides a general roadmap for combination immunotherapy against gliomas and other cancer types.

Original languageEnglish
Pages (from-to)4369-4380
Number of pages12
JournalClinical Cancer Research
Volume26
Issue number16
DOIs
StatePublished - 15 Aug 2020
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2020 American Association for Cancer Research.

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