Copyright: ©Author(s) 2026.
World J Gastroenterol. Apr 21, 2026; 32(15): 115226
Published online Apr 21, 2026. doi: 10.3748/wjg.v32.i15.115226
Published online Apr 21, 2026. doi: 10.3748/wjg.v32.i15.115226
Figure 8 High-frequency irreversible electroporation combined with BMS-1 and R848 elicits systemic antitumor immunity by modulating splenic immune cell subsets.
A and B: Proportion of splenic CD3+ CD4+ T cells; C and D: Proportion of splenic CD3+ CD8+ T cells; E and F: Proportion of splenic CD4+ CD25+ FOXP3+ Tregs; G and H: Proportion of splenic CD11c+ CD80+ CD86+ dendritic cells; I-L: Polarization of splenic macrophages: Proportion of F4/80+ CD11b+ CD86+ M1 and F4/80+ CD11b+ CD206+ M2 macrophages and the M1/M2 macrophage ratio. Each panel shows representative flow cytometry plots alongside quantitative data (n = 5). aP < 0.05, bP < 0.01, cP < 0.001, and dP < 0.0001. H-FIRE: High-frequency irreversible electroporation.
- Citation: Huang SM, Zhang XB, Li J, Zhang GH, Zhang X, Wei YT, Sun H, Ma L, Wang ZJ, Yao DX, Shi HJ, Wang T, Xiao YY. High-frequency irreversible electroporation synergizes with PD-1/PD-L1 inhibitor BMS-1 and TLR7/8 agonist R848 to potentiate liver cancer antitumor immunity. World J Gastroenterol 2026; 32(15): 115226
- URL: https://www.wjgnet.com/1007-9327/full/v32/i15/115226.htm
- DOI: https://dx.doi.org/10.3748/wjg.v32.i15.115226