第二军医大学学报
第二軍醫大學學報
제이군의대학학보
ACADEMIC JOURNAL OF SECOND MILITARY MEDICAL UNIVERSITY
2001年
1期
32-35
,共4页
刘艳君%田野苹%曹雪涛%张明徽%厉永建%周正芳%郑玲莉
劉豔君%田野蘋%曹雪濤%張明徽%厲永建%週正芳%鄭玲莉
류염군%전야평%조설도%장명휘%려영건%주정방%정령리
巨噬细胞游走抑制因子%疫苗,合成%T淋巴细胞%基因疗法
巨噬細胞遊走抑製因子%疫苗,閤成%T淋巴細胞%基因療法
거서세포유주억제인자%역묘,합성%T림파세포%기인요법
目的:研究T细胞在巨噬细胞游走 抑制因子(MIF)基因修饰的瘤苗诱导抗肿瘤免疫反应中的作用。方法:将重组MIF腺病毒转染小鼠FBL3红白血病细胞制成的瘤苗接种于小鼠体内,观察脾脏和淋 巴结中T细胞数量和功能的改变。结果:经MIF基因修饰的瘤苗免疫后 ,小鼠脾细胞和腹股沟引流淋巴结细胞数量明显增多,脾细胞CTL活性显著增强,引流淋巴 结中CD3+、CD28+、CD4+和CD8+ T细胞百分率均较对照组增加。MIF基因修饰的 瘤苗免疫对小鼠受野生型FBL3肿瘤细胞再攻击具有明显的保护作用。结论:MIF基因修饰的瘤苗能诱导T细胞介导的抗肿瘤免疫反应,有可能作为肿瘤基因治疗的 候选者。
目的:研究T細胞在巨噬細胞遊走 抑製因子(MIF)基因脩飾的瘤苗誘導抗腫瘤免疫反應中的作用。方法:將重組MIF腺病毒轉染小鼠FBL3紅白血病細胞製成的瘤苗接種于小鼠體內,觀察脾髒和淋 巴結中T細胞數量和功能的改變。結果:經MIF基因脩飾的瘤苗免疫後 ,小鼠脾細胞和腹股溝引流淋巴結細胞數量明顯增多,脾細胞CTL活性顯著增彊,引流淋巴 結中CD3+、CD28+、CD4+和CD8+ T細胞百分率均較對照組增加。MIF基因脩飾的 瘤苗免疫對小鼠受野生型FBL3腫瘤細胞再攻擊具有明顯的保護作用。結論:MIF基因脩飾的瘤苗能誘導T細胞介導的抗腫瘤免疫反應,有可能作為腫瘤基因治療的 候選者。
목적:연구T세포재거서세포유주 억제인자(MIF)기인수식적류묘유도항종류면역반응중적작용。방법:장중조MIF선병독전염소서FBL3홍백혈병세포제성적류묘접충우소서체내,관찰비장화림 파결중T세포수량화공능적개변。결과:경MIF기인수식적류묘면역후 ,소서비세포화복고구인류림파결세포수량명현증다,비세포CTL활성현저증강,인류림파 결중CD3+、CD28+、CD4+화CD8+ T세포백분솔균교대조조증가。MIF기인수식적 류묘면역대소서수야생형FBL3종류세포재공격구유명현적보호작용。결론:MIF기인수식적류묘능유도T세포개도적항종류면역반응,유가능작위종류기인치료적 후선자。
Objective: To investigate the role of T cell in the antitumor immune responses induced by MIF gene-modified tumor vaccine. Methods: MIF gene was transferred into FBL3 erythroleukemia cel l by adenovirus carrier and a new type of tumor vaccine was prepared. The chang es of the number and the function of T cell in spleen and lymph node was observe d. Results: After the mice were immunized with MIF gene-m odified FBL3 vaccine, the number of lymphocyte in spleens and lymph nodes increa sed markedly and the specific CTL activities of splenocytes also increased great ly. FACS analysis showed that the CD3+, CD4+, CD8+ T cells and CD28 posi tive cells in draining lymph nodes of MIF-FBL3 group mice increased more marked ly than that of control groups. When the wild type FBL3 cells were injected into the mice immunized with MIF gene-modified FBL3 vaccine, the growth of tumors w ere obviously inhibited and the survival rate of the mice was increased. Conclusion: It is suggested that MIF gene-modified tumor vaccine can induce specific antitumor immune responses mediated by T cells and may be a candidate for gene therapy of tumor.