中国肿瘤生物治疗杂志
中國腫瘤生物治療雜誌
중국종류생물치료잡지
CHINESE JOURNAL OF CANCER BIOTHERAPY
2000年
4期
288-290
,共3页
吴桂臣%罗荣城%韩焕兴%尤长宣%丁雪梅%李爱民%王传斌%张鸣江
吳桂臣%囉榮城%韓煥興%尤長宣%丁雪梅%李愛民%王傳斌%張鳴江
오계신%라영성%한환흥%우장선%정설매%리애민%왕전빈%장명강
肝细胞癌%裸鼠%放射免疫显像%HBsAg%单克隆抗体
肝細胞癌%裸鼠%放射免疫顯像%HBsAg%單剋隆抗體
간세포암%라서%방사면역현상%HBsAg%단극륭항체
hepatoma%nude mice%radioimmunoimaging%HBsAg%monoelonal antibody
目的:在人源抗HBs Fab表达载体构建、抗体片段表达及纯化成功后,进行放射免疫显像研究,以评价其在动物模型中的免疫导向活性。方法:用131I标记人源抗HBs Fab,经腹腔注射l,3,5,7 d后行裸鼠人肝癌模型放射免疫显像,于第7天作组织分布测定,并以鼠源抗HBsAg单抗为对照进行比较。结果:实验组在标记抗体注入后第3天即获阳性显像,第5天更加清晰,此时人源抗HBs Fab、鼠源单抗及无关Fab的瘤/肝放射性比值分别为5>4,4>0和0>9。结论:人源抗HBs Fab具有良好的导向活性,为其用于肝癌的导向治疗提供了实验依据。
目的:在人源抗HBs Fab錶達載體構建、抗體片段錶達及純化成功後,進行放射免疫顯像研究,以評價其在動物模型中的免疫導嚮活性。方法:用131I標記人源抗HBs Fab,經腹腔註射l,3,5,7 d後行裸鼠人肝癌模型放射免疫顯像,于第7天作組織分佈測定,併以鼠源抗HBsAg單抗為對照進行比較。結果:實驗組在標記抗體註入後第3天即穫暘性顯像,第5天更加清晰,此時人源抗HBs Fab、鼠源單抗及無關Fab的瘤/肝放射性比值分彆為5>4,4>0和0>9。結論:人源抗HBs Fab具有良好的導嚮活性,為其用于肝癌的導嚮治療提供瞭實驗依據。
목적:재인원항HBs Fab표체재체구건、항체편단표체급순화성공후,진행방사면역현상연구,이평개기재동물모형중적면역도향활성。방법:용131I표기인원항HBs Fab,경복강주사l,3,5,7 d후행라서인간암모형방사면역현상,우제7천작조직분포측정,병이서원항HBsAg단항위대조진행비교。결과:실험조재표기항체주입후제3천즉획양성현상,제5천경가청석,차시인원항HBs Fab、서원단항급무관Fab적류/간방사성비치분별위5>4,4>0화0>9。결론:인원항HBs Fab구유량호적도향활성,위기용우간암적도향치료제공료실험의거。
Objective: To evaluate the targeting activity in the animal model with human hepatoma, the 131I-human antiHBsAg Fab radioimmunoimaging was explored. Methods: Radioimmunoimagings were taken on different intervals after injection of 131 I-human anti-HBsAg Fab to the nude mice and tissue distribution was measured. The human anti-HBsAg Fab was compared with the murine monoclonal antibodies. Results: The experimental group developed tumor positive images after 3 days of radio-labeled monoclonal antibodies injection, and the peak accumulation of radio-activity on the 5th day.Statistics indicated the tumor/liver ratio of the human anti-HBsAg Fab, murine monoclonal antibodies and the control groups were 5.4,4.0 and 0.9 respectively on the 7th day. Conclusions: Our results suggest that the 131 I-human anti-HB-sAg Fab has a considerable targeting activity, and provide an evidence that it can be used as a novel humanized carrer for targeting therapy of hepatoma.