Objective To observe the effect of aCD 3 McAb on PBMC and TIL.

目的　观察抗人CD3单抗(aCD3McAb) 对单核细胞(PBMC) 和肿瘤组织中提取的浸润淋巴细胞(TIL)增殖的影响.

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In some of T 1 DM patients, AIRE gene expressions in PBMC were defective.

部分T1DM病人PBMC上AIRE表达缺失.

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Conclusions DcR 3 gene of PBMC over express in patients with IPF.

结论　IPF病人PBMC中DcR3基因的表达水平增高.

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Two target cells were used to detect the antibody - dependent cytotoxicity ( ADCC ) function of PBMC.

选用绵羊红细胞(SRBC) 和鸡红细胞(CRBC)作为靶细胞,用微量比色法检测人外周血单个核细胞 ( PBMC ) 的抗体依赖细胞介导的细胞毒(ADCC)活性.

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After the PBMC were transfected by Ad EWS - FLI 1 , the EWS - FLI 1 mRNA was detected by ( RT - PCR . )

转染PBMC后,RT -PCR 证实有EWS -FLI1mRNA的 转录.

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The positive rate of MAGE mRNA in the PBMC was closely correlated with the TNM stages.

乳腺癌患者PBMC中两种MAGE基因mRNA的检出率与肿瘤TNM分期密切相关.

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Conclusion CpG ODN may stimulate PBMC activity, and improve the dilling activity of PBMC on HO 8910.

结论CpGODN可刺激PBMC增殖, 提高PBMC的杀伤活性,从而增强机体的特异性和非特异性免疫效应.

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CONCLUSION: AGEP enhanced MCP - 1 mRNA expression in human PBMC.

结论: AGEP能增加人血单核巨噬细胞MCP -1 基因的表达.

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The PBMC - ADCC activity in 40 normal adults was 43.52±10.18％ ( mean ± SD ) .

40名正常人的ADCC活性为 43.52±10.18%.

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Objective To amphfy enough V 7 9 V δ2 T cells for the adoptive therapy of tumor.

目的体外以仲丁胺刺激健康人外周血PBMC中 Vγ9Vδ2T细胞 的增殖,为γδT细胞的过继免疫治疗建立效应细胞制备平台.

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There are 8.825 + 2.958 adherent cells per 100 peripheral blood mononuclear cells.

每100个外周血单个核细胞(PBMC)可获得8.825±2.958个贴壁细胞.

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