Treatment of an aggressive orthotopic murine glioblastoma model with combination checkpoint blockade and a multivalent neoantigen vaccine

• Published in: Neuro-oncology (Charlottesville, Va.) Vol. 22; no. 9; pp. 1276 - 1288
• Main Authors: Liu, Connor J, Schaettler, Maximilian, Blaha, Dylan T, Bowman-Kirigin, Jay A, Kobayashi, Dale K, Livingstone, Alexandra J, Bender, Diane, Miller, Christopher A, Kranz, David M, Johanns, Tanner M, Dunn, Gavin P
• Format: Journal Article
• Language: English
• Published: US Oxford University Press 29-09-2020
• Subjects: Animals; Antigens, Neoplasm; Basic and Translational Investigations; CD8-Positive T-Lymphocytes; Glioblastoma - therapy; Humans; Immunotherapy; Lymphocytes, Tumor-Infiltrating; Mice; Tumor Microenvironment; Vaccines, Combined; immunogenomics; neoantigen; glioblastoma; personalized vaccination
• ISSN: 1522-8517; 1523-5866
• DOI: 10.1093/neuonc/noaa050

Abstract
Background
Although clinical trials testing immunotherapies in glioblastoma (GBM) have yielded mixed results, new strategies targeting tumor-specific somatic coding mutations, termed “neoantigens,” represent promising therapeutic approaches. We characterized the microenvironment and neoantigen landscape of the aggressive CT2A GBM model in order to develop a platform to test combination checkpoint blockade and neoantigen vaccination.
Methods
Flow cytometric analysis was performed on intracranial CT2A and GL261 tumor-infiltrating lymphocytes (TILs). Whole-exome DNA and RNA sequencing of the CT2A murine GBM was employed to identify expressed, somatic mutations. Predicted neoantigens were identified using the pVAC-seq software suite, and top-ranking candidates were screened for reactivity by interferon-gamma enzyme linked immunospot assays. Survival analysis was performed comparing neoantigen vaccination, anti-programmed cell death ligand 1 (αPD-L1), or combination therapy.
Results
Compared with the GL261 model, CT2A exhibited immunologic features consistent with human GBM including reduced αPD-L1 sensitivity and hypofunctional TILs. Of the 29 CT2A neoantigens screened, we identified neoantigen-specific CD8+ T-cell responses in the intracranial TIL and draining lymph nodes to two H2-Kb restricted (Epb4H471L and Pomgnt1R497L) and one H2-Db restricted neoantigen (Plin2G332R). Survival analysis showed that therapeutic neoantigen vaccination with Epb4H471L, Pomgnt1R497L, and Plin2G332R, in combination with αPD-L1 treatment was superior to αPD-L1 alone.
Conclusions
We identified endogenous neoantigen specific CD8+ T cells within an αPD-L1 resistant murine GBM and show that neoantigen vaccination significantly augments survival benefit in combination with αPD-L1 treatment. These observations provide important preclinical correlates for GBM immunotherapy trials and support further investigation into the effects of multimodal immunotherapeutic interventions on antiglioma immunity.
Key Points
1. Neoantigen vaccines combined with checkpoint blockade may be promising treatments.
2. CT2A tumors exhibit features of human GBM microenvironments.
3. Differential scanning fluorimetry assays may complement in silico neoantigen prediction tools.