Tumor vaccine with IL-33 (interleukin-33) used as therapeutic target
A technology of interleukin and anti-tumor immunity, applied in the field of breast cancer vaccines, can solve problems such as threats to women's life and health and patient death
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Embodiment 1
[0017] Example 1: Induced expression and purification of HBcAg-33
[0018] The induced expression and purification methods of HBcAg-33 are as described in the patent > (ZL 2014 1 0248884.2). According to the steps of this method, HBcAg-33 VLPs and carrier HBcAg VLPs were obtained as immunogens for subsequent experiments.
Embodiment 2
[0019] Example 2: Preventive immunization strategy for mice
[0020] Balb / c female mice at 6-8 weeks were randomly divided into 3 groups, 8 rats / group, which were vaccine group, vehicle group and PBS group respectively. Immunization forms such as figure 1 As shown, the purified HBcAg-33 VLPs, carrier HBcAg VLPs, and PBS were subcutaneously immunized on the back of the corresponding group respectively, and each animal was immunized once every two weeks at an injection dose of 100ug, for a total of 3 times. One week after each immunization, blood was collected from the saphenous vein of the thigh of the mice to detect the antibody level. Such as figure 2 As shown, the antibody titer can reach up to 409600.
Embodiment 3
[0021] Example 3: Establishment of an orthotopic model of mouse breast cancer:
[0022] First, in RPMI-1640 medium containing 10% FBS, 1% penicillin and streptomycin mixed solution, at 37°C, 5% CO 2 4T1 tumor cells were cultured in the incubator, and 4T1 tumor cells were injected into the fourth abdominal fat pad of mice every two weeks after the last immunization, 1×10 per mouse. 5 cell, the tumor was formed on the 10th day, the tumor was measured every two days, the tumor growth curve was drawn, and the tumor growth was monitored. image 3 shown.
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