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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The influence of anti-cancer therapies on lymphocyte subpopulations of lung cancer patients.
The influence of anti-cancer therapies on lymphocyte subpopulations of lung cancer patients.
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本研究表明,不同类型的抗癌治疗会影响非小细胞肺癌患者的淋巴细胞亚群。
2018年1月至2020年3月,莱比锡肺病诊所连续纳入32例NSCLC患者。使用BD Biosciences的FACS Canto II流式细胞仪,在计划治疗前及治疗期间进行免疫表型分析,每位患者最多观察7个时间点,评估130项免疫学参数。
免疫治疗(p=0.032)、免疫化疗(p=0.030)及抗VEGF抗体治疗(p=0.024)后,绝对过渡型B细胞计数显著增加。术后辅助化疗后,B细胞绝对计数和比例也显著升高(p=0.023);而化疗后过渡型B细胞绝对计数和比例显著降低(p=0.001)。免疫治疗(p=0.031)和免疫化疗(p=0.030)后,活化细胞毒性T细胞显著增加。NSCLC患者总生存率为31%。
不同抗癌疗法会影响NSCLC患者的淋巴细胞亚群。仍需开展更大规模、多中心研究,以验证这些结果并评估淋巴细胞亚群的预后价值。
A total of 32 consecutive NSCLC patients were recruited at Pulmonology Clinic, Leipzig from January 2018 to March 2020 and enrolled in this study. Immunophenotyping was done using a FACS Canto II flow cytometer (BD Biosciences) before the administration of the planned therapy and during therapy with up to 7 observational windows for each patient targeting 130 immunologic parameters.
Absolute transitional B cells was significantly increased after immunotherapy (p = 0.032), immunochemotherapy (p = 0.030), and antibodies against VEGF (p = 0.024). Similarly, absolute counts and percentage of B cells were significantly increased after adjuvant chemotherapy (p = 0.023). However, absolute counts and percentage of transitional B cells are significantly decreased after chemotherapy (p = 0.001). Activated cytotoxic T cells were significantly increased after immunotherapy (p = 0.031) and immunochemotherapy (p = 0.030). The overall survival rate of NSCLC patients was 31%.
In conclusion, this study suggests that different types of anti-cancer therapies affect lymphocyte subpopulations of NSCLC patients. Further large-scale and multicentre studies are required to confirm our results and to evaluate the prognostic value of lymphocyte subpopulations.
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