Systemic viral vector vaccination induces brain resident memory T cells to drive anti-glioblastoma immunity
Steffke, E. E.; Latifi, L.; Hana, T.; Hara, A.; Coombs, M.; Spurgeon, J.; McAuliffe, J.; Pereira-Almeida, V.; Wicki, A.; Abdel Malak, S.; Noblecourt, L.; Huguely Wilkinson, C.; Hancock, J.; Panetti, S.; Kim, H.; Anderson, B.; Cam-El Makranz, C.; Briceno, N.; Zhang, M.; Zhang, W.; Davis, D.; Song, H.; Bryan, M. E.; Okada, H.; Gilbert, M.; Leung, C. S. K.; Van den Eynde, B. J.; Terabe, M.
Show abstract
Glioblastoma is a lethal brain tumor that is unresponsive to current cancer immunotherapeutic approaches, including immune checkpoint blockade (ICB). This suggests that initial priming of T cells, rather than their expansion and licensing as effectors, is a restricting feature in this tumor setting. To overcome the limited initiation of CD8+ T cell responses, we employed a strong heterologous prime-boost vaccination with the simian adenovirus ChAdOx1 and poxvirus modified vaccinia Ankara (MVA). Vaccination conferred therapeutic efficacy against orthotopic, immune checkpoint-blockade (ICB)-refractory SB28 murine glioblastoma. Vaccination was effective against both the murine tumor antigen, P1A, and a newly identified glioblastoma-associated antigen, Gpr149. Additional treatment with ICB provided no additional benefit. Systemic ChAdOx1/MVA vaccination induced robust infiltration of antigen-specific T cells in tumor-challenged brains, the majority of which exhibited a CD103+CD69+CD8+ tissue-resident memory (TRM)-like phenotype. These cells were polyfunctional, durable in brains with sustained tumor control, and mediated tissue-specific immunological memory. Moreover, intracranial adoptive transfer of glioblastoma-derived antigen-specific TRM-like cells was sufficient to protect naive recipients from subsequent orthotopic tumor challenge. Together, these findings establish that viral vector vaccination can generate tumor-specific TRM-like cells that mediate effective anti-glioblastoma immunity, providing a rationale for clinical evaluation of ChAdOx1/MVA-based strategies in glioblastoma.
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