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Pd 1 mab

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PD-1 mAb is a monoclonal antibody that specifically binds to the Programmed Cell Death 1 (PD-1) receptor. PD-1 is an immune checkpoint protein expressed on the surface of T cells, B cells, and other immune cells. The core function of PD-1 mAb is to block the interaction between PD-1 and its ligands, PD-L1 and PD-L2, thereby modulating immune responses.

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3 protocols using pd 1 mab

1

Combination Therapy Inhibits Tumor Growth

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Six-week-old BALB/c mice were purchased from Shanghai SLAC Animal Laboratory Co. Ltd. (Shanghai, China) and fed at the Animal Center of Tongji University. CT26 cells (1 × 106 cells) were administered into the right limbs of BALB/c mice. Tumor size was determined on the indicated days using the formula (width)2 × length/2. After the tumor grew into 100 mm3, mice were treated with different strategies and segregated into four groups according to the tumor therapy received: phosphate-buffer saline (PBS), STAT3 inhibitor (5 µM, MedChemExpress, New Jersey, USA), PD-1 mAb (10 µg/mL, Bioxcell, Lebanon, NH, USA) or combinatorial treatment with STAT3 inhibitor (5 µM) and PD-1 mAb (10 µg/mL), a replicate for each treatment group for each day for intraperitoneal injection. At the endpoint of experiments, all mice were euthanized, and organs were harvested for flow cytometry and histopathological analysis.
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2

Combinatorial Cancer Immunotherapy in Mice

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Six‐week‐old BALB/c mice were included in the study. CT26 cells (5 × 105 cells) were administered into the right limbs of immunocompetent BALB/c mice. Seven days after tumor cell injection (day 0), tumors were measured using the formula (width)2 × length/2. Mice were segregated into four groups according to the tumor therapy received: PBS, OncoAd (5 × 108 VPs of each virus in 100 μl), PD‐1 mAb (10 μg ml−1; Bioxcell) or combinatorial treatment with OncoAd (5 × 108 VPs of each virus in 100 μl) and PD‐1 mAb (10 μg ml−1; Bioxcell). On day 0, OncoAd or PBS were directly injected into the tumor. A second dose (PBS, OncoAd [5 × 108 VPs of each virus in 100 μl]) was administered on day 4. Anti‐PD‐1 therapy developed herein was administered on days 8, 10, and 12 intraperitoneally, and a replicate for each treatment group for each day. On day 14, all mice were euthanized and organs were harvested for flow cytometry and histopathological analysis.
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3

Tumor Immunotherapy Protocol with PD-1 mAb and HSA-IL21

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HSA-IL21 (the half-life extended IL21 was kindly provided by Anwita Biosciences, CA, USA), PD-1mAb (clone:J43), hamster IgG were purchased from Bioxcell company (catalog no. BE0091) for tumor therapy. For Flow cytometry, CD45 (clone: 30-F11), CD4 (clone: GK1.5), CD8 (clone: 53–6.7), NK1.1 (clone: PK136), B220 (clone: RA3-6B2), Foxp3 (MF-14), PD-1(29F.1A12), Tim-3 (clone: RMT3-23), Lag-3 (clone: C9B7W), CD39 (clone: 24DMS1), CD62L (clone: MEL-14), CD44 (clone: IM7), CD103 (clone: M290), CD69 (clone: H1.2F3), IFN-γ (clone: XMG1.2), GzmB (clone: QA16A02), CD11b (clone: M1/70), Ly6C (clone: HK1.4), Ly6G (clone: 1A8), Gr-1 (clone: RB6-8C5), CD24 (clone: M1/69), F4/80 (clone: BM8), CD11C (clone: N418), CD206 (clone: MR6F3), Arginase 1 (clone: A1exF5) were purchased from Biolegend ebioscience or BD Bioscience. Zombie NIR dye was purchased from Biolegend.
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