论文部分内容阅读
以 ̄(35)S标记抗人脑胶质瘤单克隆抗体SZ39制备成导向放疗剂 ̄(35)S-MAbSZ39,荷瘤鼠体内治疗研究表明103.6MBq ̄(35)S-MAb ̄(35)SZ39对肿瘤可产生抑制作用,阻制肿瘤生长一周左右,给药后26天,抑制率达50%.流式细胞计数仪分析,导向治疗后肿瘤细胞DNA合成受抑,S期细胞蓄积,G1期细胞受阻,有细胞周期同步化趋势,有利于再次导向放射治疗。病理学检查证实, ̄(35)S-MAb ̄(35)SZ39对脊髓正常组织无明显毒付作用。以上结果显示了 ̄(35)S-MAb ̄(35)SZ39对人脑胶质瘤放射免疫治疗的潜在价值。
A 35S-labeled anti-human glioma monoclonal antibody SZ39 was prepared as a directed radiotherapy agent ̄(35)S-MAbSZ39. In vivo treatment studies in tumor-bearing mice showed 103.6MBq ̄(35)S-MAb ̄ (35 ) SZ39 can inhibit the growth of tumors, inhibit tumor growth for about one week, and after 26 days of administration, the inhibition rate reaches 50%. Flow cytometric analysis showed that DNA synthesis of tumor cells was inhibited after targeted treatment, cell accumulation was observed in S phase, G1 phase cells were blocked, and cell cycle synchronization was observed, which was conducive to redirected radiation therapy. Pathological examination confirmed that ̄(35)S-MAb ̄(35)SZ39 had no obvious toxic effect on normal spinal cord tissue. The above results show the potential value of ̄(35)S-MAb ̄(35)SZ39 for radioimmunotherapy of human glioma.