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首页> 外文期刊>International journal of hyperthermia: The official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group >Melan-A specific CD8+ T lymphocytes after hyperthermic isolated limb perfusion: A pilot study in patients with in-transit metastases of malignant melanoma
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Melan-A specific CD8+ T lymphocytes after hyperthermic isolated limb perfusion: A pilot study in patients with in-transit metastases of malignant melanoma

机译:高温隔离肢体灌注后的Melan-A特异性CD8 + T淋巴细胞:恶性黑色素瘤转移性转移患者的一项初步研究

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Purpose: Isolated limb perfusion (ILP) with hyperthermia is an effective treatment for in-transit metastases of malignant melanoma in the extremities. Preclinical studies have shown that hyperthermia may induce an immunogenic death of tumour cells. We therefore decided to study whether ILP may induce tumour-specific immune responses in the clinical setting. Method: The number of Melan-A/Mart-1 specific CD8+ T cells, as well as other phenotypically different immune cells, was recorded in peripheral blood in 12 HLA-A2+ patients with in-transit metastases undergoing hyperthermic ILP with melphalan. Results: All patients underwent ILP without any complication and with an overall response rate of 83%. No substantial changes in the number of circulating T-cells, B-cells, NK-cells or monocytes were observed during follow-up. Four out of 12 patients showed an elevation of Melan-A+ CD8+ T-cells 4 weeks after ILP. Conclusion: We here report our preliminary observations that a small increase in tumour-specific T-cells could be seen in a subpopulation of patients after ILP. However, much more work is necessary to fully delineate the systemic immune response to hyperthermic ILP.
机译:目的:孤立性肢体灌注(ILP)伴热疗是治疗四肢恶性黑色素瘤在途转移的有效方法。临床前研究表明,体温过高可能会诱导肿瘤细胞的免疫原性死亡。因此,我们决定研究在临床环境中ILP是否可以诱导肿瘤特异性免疫反应。方法:在12例HLA-A2 +转移性转移中接受美法仑高热ILP的HLA-A2 +患者的外周血中,记录了Melan-A / Mart-1特异性CD8 + T细胞以及其他表型不同的免疫细胞的数量。结果:所有患者均接受ILP治疗,无任何并发症,总缓解率为83%。在随访期间,未观察到循环中的T细胞,B细胞,NK细胞或单核细胞数量的实质性变化。 ILP后4周,四分之十二的患者显示Melan-A + CD8 + T细胞升高。结论:我们在这里报告了我们的初步观察结果,ILP后的患者亚群中可以看到肿瘤特异性T细胞的少量增加。但是,需要更多的工作来全面描述对高温ILP的全身免疫反应。

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