TY - JOUR
T1 - Synthetic High-density Lipoprotein Nanodiscs for Personalized Immunotherapy against Gliomas
AU - Scheetz, Lindsay
AU - Kadiyala, Padma
AU - Sun, Xiaoqi
AU - Son, Sejin
AU - Najafabadi, Alireza Hassani
AU - Aikins, Marisa
AU - Lowenstein, Pedro R.
AU - Schwendeman, Anna
AU - Castro, Maria G.
AU - Moon, James J.
N1 - Publisher Copyright:
© 2020 American Association for Cancer Research.
PY - 2020/8/15
Y1 - 2020/8/15
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85089728769&partnerID=8YFLogxK
U2 - 10.1158/1078-0432.CCR-20-0341
DO - 10.1158/1078-0432.CCR-20-0341
M3 - Article
C2 - 32439701
AN - SCOPUS:85089728769
SN - 1078-0432
VL - 26
SP - 4369
EP - 4380
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 16
ER -