中国组织工程研究与临床康复
中國組織工程研究與臨床康複
중국조직공정연구여림상강복
JOURNAL OF CLINICAL REHABILITATIVE TISSUE ENGINEERING RESEARCH
2010年
18期
3318-3322
,共5页
人红细胞膜%S180肉瘤%瘤内注射%异种抗原%器官移植
人紅細胞膜%S180肉瘤%瘤內註射%異種抗原%器官移植
인홍세포막%S180육류%류내주사%이충항원%기관이식
背景:异种抗原的免疫原性比较强,容易引起较强的免疫应答.如果将异种抗原直接引入肿瘤内部,在肿瘤内部引发一系列免疫反应,有可能逆转肿瘤微环境的免疫抑制状态,达到抗肿瘤的目的.目的:评价人红细胞膜抗原瘤内注射对荷S180肉瘤小鼠肿瘤生长的抑制作用.方法:复制昆明小鼠S180肉瘤皮下瘤模型,瘤内注射质量浓度为5 g/L的人红细胞膜抗原或生理盐水,连续注射5 d,记录注射前及注射第3,7,14天肿瘤体积变化.同时设肿瘤细胞与人红细胞膜抗原同时接种组、免疫后瘤内注射人红细胞膜抗原组、免疫后瘤内注射生理盐水组.另取60只小鼠复制S180肉瘤皮下瘤模型,免疫及瘤内注射人红细胞膜抗原或生理盐水同前.注射第14天每组处死6只小鼠,肿瘤称质量,行病理学分析,每组剩余小鼠继续观察生存情况.结果与结论:各组小鼠肿瘤体积逐渐增大,第14天人红细胞膜抗原与肿瘤细胞同时接种组、免疫后人红细胞膜抗原瘤内注射组、人红细胞膜抗原瘤内注射组肿瘤体积均小于瘤内注射生理盐水组.瘤内注射人红细胞膜抗原可显著降低肿瘤质量.瘤内注射人红细胞膜抗原后镜下可见肿瘤细胞坏死、淋巴细胞等炎症细胞浸润.未观察到各组小鼠生存期有明显差别.结果表明异种红细胞膜抗原瘤内注射可以抑制小鼠S180肉瘤肿瘤生长.
揹景:異種抗原的免疫原性比較彊,容易引起較彊的免疫應答.如果將異種抗原直接引入腫瘤內部,在腫瘤內部引髮一繫列免疫反應,有可能逆轉腫瘤微環境的免疫抑製狀態,達到抗腫瘤的目的.目的:評價人紅細胞膜抗原瘤內註射對荷S180肉瘤小鼠腫瘤生長的抑製作用.方法:複製昆明小鼠S180肉瘤皮下瘤模型,瘤內註射質量濃度為5 g/L的人紅細胞膜抗原或生理鹽水,連續註射5 d,記錄註射前及註射第3,7,14天腫瘤體積變化.同時設腫瘤細胞與人紅細胞膜抗原同時接種組、免疫後瘤內註射人紅細胞膜抗原組、免疫後瘤內註射生理鹽水組.另取60隻小鼠複製S180肉瘤皮下瘤模型,免疫及瘤內註射人紅細胞膜抗原或生理鹽水同前.註射第14天每組處死6隻小鼠,腫瘤稱質量,行病理學分析,每組剩餘小鼠繼續觀察生存情況.結果與結論:各組小鼠腫瘤體積逐漸增大,第14天人紅細胞膜抗原與腫瘤細胞同時接種組、免疫後人紅細胞膜抗原瘤內註射組、人紅細胞膜抗原瘤內註射組腫瘤體積均小于瘤內註射生理鹽水組.瘤內註射人紅細胞膜抗原可顯著降低腫瘤質量.瘤內註射人紅細胞膜抗原後鏡下可見腫瘤細胞壞死、淋巴細胞等炎癥細胞浸潤.未觀察到各組小鼠生存期有明顯差彆.結果錶明異種紅細胞膜抗原瘤內註射可以抑製小鼠S180肉瘤腫瘤生長.
배경:이충항원적면역원성비교강,용역인기교강적면역응답.여과장이충항원직접인입종류내부,재종류내부인발일계렬면역반응,유가능역전종류미배경적면역억제상태,체도항종류적목적.목적:평개인홍세포막항원류내주사대하S180육류소서종류생장적억제작용.방법:복제곤명소서S180육류피하류모형,류내주사질량농도위5 g/L적인홍세포막항원혹생리염수,련속주사5 d,기록주사전급주사제3,7,14천종류체적변화.동시설종류세포여인홍세포막항원동시접충조、면역후류내주사인홍세포막항원조、면역후류내주사생리염수조.령취60지소서복제S180육류피하류모형,면역급류내주사인홍세포막항원혹생리염수동전.주사제14천매조처사6지소서,종류칭질량,행병이학분석,매조잉여소서계속관찰생존정황.결과여결론:각조소서종류체적축점증대,제14천인홍세포막항원여종류세포동시접충조、면역후인홍세포막항원류내주사조、인홍세포막항원류내주사조종류체적균소우류내주사생리염수조.류내주사인홍세포막항원가현저강저종류질량.류내주사인홍세포막항원후경하가견종류세포배사、림파세포등염증세포침윤.미관찰도각조소서생존기유명현차별.결과표명이충홍세포막항원류내주사가이억제소서S180육류종류생장.
BACKGROUND: Herterologous antigen has strong immunogenicity and easily induces immunological response. Introduction of herterologous antigen into tumor may induce a serial of immunological reactions in the tumor and may reverse the immunosuppression of tumor microenvironment to treat tumor.OBJECTIVE: To evaluate the antitumor efficacy of intratumoral injection of human erythrocyte membrane antigens in micebearing S180 sarcoma.METHODS: Kunming mice bearing S180 sarcoma model were established and treated with 5 g/L human erythrocyte membrane antigens suspension or normal saline for five days. Tumor volume was calculated before the first injection and 3, 7, and 14 days after the first injection. In addition, the tumor cells in combination with human erythrocyte membrane antigens group, the njectionof saline group (the control group), and the injection of human erythrocyte membrane antigens or saline group (pre-immunized by suspension of human erythrocyte of blood group type A). Another 60 mice bearing S180 sarcoma were established and subjected to the above pre-immunization and injection of saline or human erythrocyte membrane antigens. Six mice selected from each group were sacrificed 14 days after the first injection, and tumors were weighed, followed by histological examination. Survival of remainders in each group was observed.RESULTS AND CONCLUSION: Tumor volumes in each group increased gradually. Tumor volumes in the human erythrocyte membrane antigens injection group, the tumor cells in combination with human erythrocyte membrane antigens group, and the human erythrocyte membrane antigens injection group (immunized) were smaller than the control group, Intratumoral injection of human erythrocyte membrane antigens significantly reduced tumor weights. Tumor necrosis, infiltration of inflammatory cells such as lymphocytes were observed in tumor tissues section examination following the intratumoral injection of human erythrocyte membrane antigens. The mouse survival time showed no statistical difference among different groups. Intratumoral injection of heteroloaous ervthrocvte membrane antiaens can inhibit tumor arowth of S180 sarcoma bearina mice.