热休克蛋白96白血病抗原肽抗髓系白血病效应的研究  被引量:1

The anti-leukemia effect of heat shock protein-peptide complex-96

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作  者:方群[1] 张卫平[1] 赵洪灿[2] 范剑[3] 沈丹[3] 童向民[3] 

机构地区:[1]浙江中医药大学附属第三医院感染科,杭州310009 [2]杭州市第一人民医院检验科,310006 [3]浙江大学医学院附属第一医院血液科,杭州310003

出  处:《中华危重症医学杂志(电子版)》2013年第1期12-16,共5页Chinese Journal of Critical Care Medicine:Electronic Edition

基  金:国家自然科学基金(81172250);浙江省自然科学基金(LY12H16015);浙江省卫生厅(2011ZDA008;2012ZB070);杭州市科技局项目(20120533Q02)

摘  要:目的研究热休克蛋白96(HSP-gp96)白血病抗原肽的抗白血病效应及相关机制。方法将不同的白血病细胞株(K562、HL-60、U937)分别分为A、B细胞株组,A组加预先构建的HSP-gp96重组腺病毒感染,B组不加以感染。将两组细胞株均制备为相应的抗原肽(分别设为A1、B1组),外周血单个核细胞诱导树突细胞(DC)后分别负载A1及B1组抗原肽以分别获取相应的DC复合物(分别设为A2、B2组)。用四甲基偶氮唑蓝反应比色法检测各组对T淋巴细胞增殖的影响,用乳酸脱氢酶释放法检测其在不同效靶比下的自然杀伤细胞(NK)活性和细胞毒性T淋巴细胞(CTL)效应,并比较K562来源的A2组复合物对3种白血病细胞株杀伤效应的不同。结果与A、B及B1组相比,3种不同细胞株的A1、A2和B2组均可刺激T淋巴细胞的增殖,同时也能增强NK细胞活性和CTL效应(P均<0.05)。其中A1、A2组对NK活性和CTL效应的增强尤为显著。且随着效靶比的增加,A1、A2和B2组NK细胞活性和CTL效应也明显增强。另外,K562细胞株制备的A2组复合物的CTL效应在K562细胞中明显增强,与HL-60及U937细胞相比,差异有统计学意义。结论 HSP-gp96白血病抗原肽抗白血病效应明显,经DC诱导后其作用增强,且后者对同源细胞株的杀伤效应具有特异性。Objective To investigate the anti-leukemia effect of heat shock protein- peptide complex-96 (HSP-gp96). Methods Human leukemia cell lines (K562, HL-60 and U937) were respectively divided into group A and group B. Only human leukemia cell lines in group A were infected with the constructed recombinant adenovirus Ad-gp96. The cell lines in groups A and B were prepared for antigen peptide and then categorized into group A1 and group B1. Peripheral blood mononuclear cell induced by dendritic ceils (DC) loading antigen peptide prepared the DC-complex (group A2 and group B2). Of each group, the proliferation of T lymphocytes was detected by methyl thiazolyl tetrazolium cytotoxicity method, and cytotoxic lymphocyte (CTL) and natural killer (NK) cell activity at different effect- target ratio was measured by lactate dehydrogenase release assay. Results Compared with groups A, B and B~, the proliferation of T lymphocytes were stimulated more remarkably in groups A~, A2 and B~ (especially in 'groups A1 and B2), the activity of NK cell and CTL were enhanced (all P 〈 0.05), and the cytotoxic effect in the leukemia cells as the effect- target ratio were higher. The gp96-peptide complex derived from K562 was more efficient in enhancing the activity of CTL than HL-60 and U937 cells. Conclusion Leukemia antigen gp96-peptide complex has a significant anti-leukemia effect, especially after stimulated by DCs. Furthermore, this anti-leukemia effect has a specificity.

关 键 词:白血病 髓样 HSP90热休克蛋白质类 树突细胞 

分 类 号:R733.7[医药卫生—肿瘤]

 

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