Fig. 5From: Dual activity of PD-L1 targeted Doxorubicin immunoliposomes promoted an enhanced efficacy of the antitumor immune response in melanoma murine modelImmune response promoted by different treatments in tumor tissue. B16OVA tumor bearing mice were administered with different treatments: saline, free Dox, Conventional Dox liposomes (LPD), LPD co-administered with 28 µg of free α-PD-L1 (mAb) or Targeted Dox liposome or immunoliposomes (LPF). Dox was intravenously injected at 3 mg/kg and eight days later, tumors were removed to evaluate different T cell subpopulations. a CD8+ cells; b Tumor specific cytotoxic T lymphocytes (Tetramer+/CD8+); c Activated cytotoxic T lymphocytes (PD1+/CD8+); d Activated CD8+ tumor specific lymphocytes. Bars show the minimum and maximum value with the mean of each treatment. Data correspond to two independent assays. n = 8 in total **p < 0.01 compared to control groupBack to article page