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Effects of dendritic cells transfected with full-length wild-type p53 and stimulated by gastric cancer lysates on immune response

机译:全长野生型p53转染树突状细胞并被胃癌裂解液刺激对免疫反应的影响

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AIM: To investigate the effects of dendritic cells (DCs) transfected with full-length wild-type p53 and stimulated by gastric cancer lysates on immune response. METHODS: The wild-type p53was transduced to DCs with adenovirus, and the DCs were stimulated by gastric cancer lysates. The surface molecules (B7-1, B7-2, MHC-Ⅰ, MHC-Ⅱ) of all DCs were detected by FACS, and the ability of the DCs to induce efficient and specific immunological response in anti-~(51)Cr-labeled target cells was studied. BALB/c mice injected with DCs and Mk28 were established, and CTL response in mice immunized with Lywt-p53DC was evaluated. Tumor-bearing mice were treated with Lywt-p53DC. RESULTS: The surface molecules of Lywt-p53DC had a high expression of B7-1 (86.70±0.07%), B7-2 (18.77±0.08%), MHC-Ⅰ (87.20±0.05%) and MHC-Ⅱ (56.70±0.07%); T lymphocytes had a specific CTL lysis ability induced by Lywt-p53DC; the CTL lysis rate was as high as 81%. The immune protection of Lywtp-53DC was obvious, the tumor diameter in Lywtp-53DC group was 3.10±0.31 mm, 2.73±0.23 mm, 3.70±0.07 mm on d 13, 16 and 19, respectively, which were smaller than control, DC, wtp53DC and LyDC group (P < 0.05). Tumor growth rate in Lywtp53DC group was slower than that in other groups (P < 0.05). CONCLUSION: DCs transfected with wild-type p53 and stimulated by gastric cancer lysates have specific CTL killing activity.
机译:目的:研究全长野生型p53转染的树突状细胞(DC)受到胃癌裂解物刺激后对免疫反应的影响。方法:用腺病毒将野生型p53转导至DC,并用胃癌裂解液刺激DC。通过FACS检测所有DC的表面分子(B7-1,B7-2,MHC-Ⅰ,MHC-Ⅱ),以及DC诱导抗〜(51)Cr-的有效和特异性免疫应答的能力。研究了标记的靶细胞。建立注射DC和Mk28的BALB / c小鼠,并评价用Lywt-p53DC免疫的小鼠的CTL应答。用Lywt-p53DC治疗荷瘤小鼠。结果:Lywt-p53DC的表面分子高表达B7-1(86.70±0.07%),B7-2(18.77±0.08%),MHC-Ⅰ(87.20±0.05%)和MHC-Ⅱ(56.70±)。 0.07%); T淋巴细胞具有由Lywt-p53DC诱导的特异的CTL裂解能力。 CTL裂解率高达81%。 Lywtp-53DC的免疫保护作用明显,Lywtp-53DC组在第13、16和19天的肿瘤直径分别为3.10±0.31 mm,2.73±0.23 mm,3.70±0.07 mm,小于对照组,DC ,wtp53DC和LyDC组(P <0.05)。 Lywtp53DC组的肿瘤生长速度低于其他组(P <0.05)。结论:转染野生型p53并受胃癌裂解物刺激的DC具有特异性的杀伤CTL的活性。

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