中国实验诊断学
中國實驗診斷學
중국실험진단학
Chinese Journal of Laboratory Diagnosis
2015年
10期
1636-1638
,共3页
赵鑫%常颖%刘玉侠%卢卫平%王宝%王哲%于鸿%王启文%王斌
趙鑫%常穎%劉玉俠%盧衛平%王寶%王哲%于鴻%王啟文%王斌
조흠%상영%류옥협%로위평%왕보%왕철%우홍%왕계문%왕빈
树突状细胞%CIK 细胞%T 淋巴细胞亚群%杀伤活性
樹突狀細胞%CIK 細胞%T 淋巴細胞亞群%殺傷活性
수돌상세포%CIK 세포%T 림파세포아군%살상활성
dendritic cells%CIK cells%T lymphocyte subsets%killing activity
目的:探讨 DC(dendritic cells)、CIK(cytokine-induced killer cells)联合培养对肺腺癌细胞 A549的杀伤活性的影响,并与单独 CIK 对 A549杀伤活性进行比较,为肿瘤生物治疗提供有效方法。方法分别培养 DC、CIK 细胞,经鉴定后进行联合培养,联合培养3天后,对 A549细胞进行杀伤活性实验,检测 DC 联合 CIK 及单独 CIK 对A549的杀伤活性,同时用流式细胞检测 DC、CIK 联合培养细胞及单独 CIK 细胞中淋巴细胞亚群的表达。结果DC联合 CIK 对 A549的杀伤活性为88.38%,CIK 对 A549的杀伤活性为66.24%,两者对 A549的杀伤活性比较有显著差异(P <0.01);DC、CIK 联合培养的淋巴细胞亚群中的 CD3+、CD4+、NK 、NKT 、CD3+ HLA-DR+、CD8+ CD28+的数量均高于 CIK 细胞。结论DC 、CIK 联合培养对肺癌细胞 A549的杀伤活性明显高于单独 CIK 对 A549的杀伤活性(P <0.01);抗肿瘤淋巴细胞(CD3+、CD4+、NK、NKT 、CD3+ HLA-DR+、CD8+ CD28+)数量也明显高于 CIK 细胞。
目的:探討 DC(dendritic cells)、CIK(cytokine-induced killer cells)聯閤培養對肺腺癌細胞 A549的殺傷活性的影響,併與單獨 CIK 對 A549殺傷活性進行比較,為腫瘤生物治療提供有效方法。方法分彆培養 DC、CIK 細胞,經鑒定後進行聯閤培養,聯閤培養3天後,對 A549細胞進行殺傷活性實驗,檢測 DC 聯閤 CIK 及單獨 CIK 對A549的殺傷活性,同時用流式細胞檢測 DC、CIK 聯閤培養細胞及單獨 CIK 細胞中淋巴細胞亞群的錶達。結果DC聯閤 CIK 對 A549的殺傷活性為88.38%,CIK 對 A549的殺傷活性為66.24%,兩者對 A549的殺傷活性比較有顯著差異(P <0.01);DC、CIK 聯閤培養的淋巴細胞亞群中的 CD3+、CD4+、NK 、NKT 、CD3+ HLA-DR+、CD8+ CD28+的數量均高于 CIK 細胞。結論DC 、CIK 聯閤培養對肺癌細胞 A549的殺傷活性明顯高于單獨 CIK 對 A549的殺傷活性(P <0.01);抗腫瘤淋巴細胞(CD3+、CD4+、NK、NKT 、CD3+ HLA-DR+、CD8+ CD28+)數量也明顯高于 CIK 細胞。
목적:탐토 DC(dendritic cells)、CIK(cytokine-induced killer cells)연합배양대폐선암세포 A549적살상활성적영향,병여단독 CIK 대 A549살상활성진행비교,위종류생물치료제공유효방법。방법분별배양 DC、CIK 세포,경감정후진행연합배양,연합배양3천후,대 A549세포진행살상활성실험,검측 DC 연합 CIK 급단독 CIK 대A549적살상활성,동시용류식세포검측 DC、CIK 연합배양세포급단독 CIK 세포중림파세포아군적표체。결과DC연합 CIK 대 A549적살상활성위88.38%,CIK 대 A549적살상활성위66.24%,량자대 A549적살상활성비교유현저차이(P <0.01);DC、CIK 연합배양적림파세포아군중적 CD3+、CD4+、NK 、NKT 、CD3+ HLA-DR+、CD8+ CD28+적수량균고우 CIK 세포。결론DC 、CIK 연합배양대폐암세포 A549적살상활성명현고우단독 CIK 대 A549적살상활성(P <0.01);항종류림파세포(CD3+、CD4+、NK、NKT 、CD3+ HLA-DR+、CD8+ CD28+)수량야명현고우 CIK 세포。
Objective To discussion of cytotoxicity effects of DC (dendritic cells)and CIK (cytokine-induced cells) co-cultured on lung adenocarcinoma cell line A549,and Compare with CIK alone on A549 killing activity,Provide an ef-fective method for tumor biotherapy.Methods respectively cultured DC,CIK cell,and co-cultured after the identifica-tion,after 3 days,to killing activity experiments on A549 cell,detect cytotoxicity of DC joint CIK and separate CIK a-gainst A549,While using flow cytometry detect lymphocyte subsets expression of DC joint CIK and CIK alone.Results The cytotoxicity of DC joint CIK on A549 was 88.38%,CIK was 66.24%,there were significant differences of cyto-toxic activity on A549(P <0.01)between,the number of lymphocyte subsets (CD3 + ,CD4 + ,NK,NKT,CD3 + HLA-DR+ ,CD8+ CD28+ cell)of DC joint CIK was significantly higher than CIK.Conclusion The killing activity of DC and CIK co-cultured on A549 lung cancer has significantly higher than that of single CIK cytotoxicity on A549(P <0.01).