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ABSTRACT: BACKGROUND
Despite aggressive treatments, GBM continues to have unacceptably high mortality rates. Immune-checkpoint blockade and ACT have shown excellent results in other solid tumors, especially in melanoma. Unfortunately, these results have not been extrapolated to GBM. We have developed a novel platform for ACT using tumor mRNA-pulsed dendritic cells(DCs) to in-vitro expand polyclonal populations of tumor-reactive T-cells. This platform has shown promising effects in preclinical brain tumor models (Flores et al OncoImmunology 2015, Wildes et al CCR 2018, Flores et al NatureComm 2018) and being evaluated in clinical trials at UF Health (NCT02465268,NCT03334305). STUDY OBJECTIVE
Evaluate whether immune-checkpoint blockade during ex-vivo expansion of antigen-spe
SUBMITTER: Ogando-Rivas E
PROVIDER: S-EPMC6846700 | biostudies-literature | 2019 Nov
REPOSITORIES: biostudies-literature