Research Article: The 41BB-agonist potentiates the therapeutic efficacy of a combined irreversible electroporation ablation treatment of lung cancer by promoting unexpected CD8 + CD103 + cDC1 and tissue-resident memory T cell responses
Abstract:
Irreversible electroporation (IRE) is a relatively new, non-thermal ablation technology for cancer treatment that requires further investigation to optimize its therapeutic efficacy. To improve IRE-ablation, we developed an IRE+Combo-treatment regimen that included the Combo adjuvants poly-I:C (pIC)/CpG, anti-PD-L1 antibody (PD-L1-Ab) and the 41BB-agonist, and investigated its anti-tumor immunity in a 3LL OVA lung cancer model. We demonstrated that inclusion of the 41BB-agonist in the IRE+Combo-ablation stimulated a more efficient CD8 + T cell response (5.3%) than that observed in the absence of 41BB-agonist (3.0%) or upon IRE ablation alone (0.4%), leading to eradication of subcutaneous 3LL OVA cancer in 75% of 3LL OVA -bearing mice. We further showed that the IRE+Combo-treatment regimen resulted in the eradication of both 3LL OVA cancer and lung tumor metastases. Interestingly, our flow cytometry analyses argued that addition of the 41BB-agonist to the IRE+Combo-ablation stimulated a higher frequency of novel CD8 + CD103 + conventional type-1 dendritic cells (cDC1) (14.4%) in tumor-drainage lymph-nodes (TDLNs) relative to control IRE+CpG/pIC/PD-L1-Ab- (7.5%) and IRE- (4.0%) treatment groups. This novel cDC1 subpopulation exhibited the most robust expression of DC maturation markers and costimulatory 41BBL and 41BB of all cDC1 subsets. The 41BB-agonist also stimulated a higher frequency of 41BB + CD103 + TCF-1 + tissue-resident memory T (T RM ) cells (14.5%) in TDLNs when compared with the two control (2.6% and 0.3%) treatment groups. Importantly, the IRE+Combo-treatment regimen was more efficient than the two control groups at converting the immunosuppressive tumor microenvironment (TME), an effect that was mitigated by reducing the frequency of inhibitory myeloid-derived suppressive cells while increasing that of immunogenic cDC1 and CD8 + T cells and rescuing T cell exhaustion. Taken together, our data establish that the 41BB-agonist potentiates the efficacy of IRE+Combo-therapy for lung cancer treatment by promoting unexpected cDC1 and T RM cell responses, and emphasize the importance of targeting this promising molecular signal to improve current cancer IRE-ablation protocols.
Introduction:
Irreversible electroporation (IRE) is a new, non-thermal form of cancer ablation technology that delivers short bursts of current to induce irreversible, nano-sized holes in cell membranes, leading to broad tumor cell apoptosis ( 1 , 2 ). Unlike thermal forms of ablation technologies like radiofrequency, high intensity focused ultrasound and microwaves that cause a “heat sink” effect and induce collateral damage to nearby tissue structures, IRE does not damage adjacent blood vessels, bile ducts and nerves or…
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