RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
肿瘤细胞治疗研究
英文原题:Natural Killer Cell Immunotherapy After Allogeneic Hematopoietic Stem Cell Transplantation in Acute Leukemia Patients: Phase I Clinical Trial.
Natural Killer Cell Immunotherapy After Allogeneic Hematopoietic Stem Cell Transplantation in Acute Leukemia Patients: Phase I Clinical Trial.
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在本研究中,我们介绍了一种激活 CD56+细胞的可行方法。尽管干预组和对照组患者的生存率在统计学上无差异,但本研究表明,第+40 天时 NK 细胞比例较高与移植后更好的生存率和更少的并发症相关。
免疫治疗为预防复发和移植并发症提供了一种有前景的方法。自然杀伤(NK)细胞在免疫系统对感染和恶性细胞的初始防御中发挥关键作用。用白细胞介素-15激活NK细胞可增强抗白血病免疫反应。我们开展了这项临床试验,以评估CD56+细胞输注在提高急性髓系白血病患者生存率和降低复发方面的安全性和有效性。
在移植后第+7天、+14天和第+21天,分别注射了递增剂量的1×10^6、3×10^6和5×10^6个白细胞介素-15激活的CD56+细胞/kg,这些细胞来源于单倍体相合供者的外周血。对患者进行不良事件监测。为了评估疗效,在第+30天和第+90天采集骨髓样本。在第+40天,评估NK细胞群体及其与患者临床状态的相关性。此外,在第+40天检查免疫重建情况。患者随访一年。
CD56+细胞输注是安全的,未伴随任何并发症。虽然干预组和对照组的生存率在统计学上没有差异,但观察到干预组有生存改善的趋势。完全缓解的患者在第+40天时NK细胞百分比较移植物排斥、复发或死亡的患者更高。
Immunotherapy offers a promising approach to prevent relapse and transplant complications. Natural killer (NK) cells play a crucial role in the immune system's initial defense against infections and malignant cells. Activation of NK cells with interleukin-15 enhances anti-leukemic immune responses. We conducted this clinical trial to evaluate the safety and efficacy of CD56 + cell infusion in increasing survival and reducing relapse in patients with acute myeloid leukemia.
Three escalating doses of 1 × 10 6 , 3 × 10 6 , and 5 × 10 6 interleukin-15-activated CD56 + cells/kg derived from peripheral blood of haploidentical donors were injected on days + 7, +14, and + 21 following transplantation. Patients were monitored for adverse events. To evaluate efficacy, bone marrow samples were taken on days + 30 and + 90. On day + 40, the population of NK cells and its correlation with patients' clinical status were evaluated. Besides, immune reconstitution was examined on day + 40. Patients were followed up for one year.
The CD56 + cells infusion was safe and not associated with any complications. While survival rates were not statistically different between the intervention and control groups, a trend toward improved survival was observed in the intervention group. Patients with complete remission showed a higher percentage of NK cells on day + 40 than patients who experienced graft rejection, relapse, or death.
In this study, we introduce a feasible method for activating CD56 + cells. Although the survival rates of patients in the intervention and control groups did not differ statistically, this study showed that a higher percentage of NK cells on day + 40 is associated with better survival and fewer complications following transplantation. TRIAL REGISTRATION: This study was registered at the Iranian Registry of Clinical Trials under code IRCT20230801058996N2 on 2023-09-10.
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