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:Impact on CD4+ CD25 High -CD127 low regulatory T (Treg) cells of neoadjuvant therapy for rectal cancer patients.
Impact on CD4+ CD25 High -CD127 low regulatory T (Treg) cells of neoadjuvant therapy for rectal cancer patients.
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Treg 细胞可能构成判断直肠癌患者新辅助治疗效果的参考。
直肠癌新辅助治疗的疗效尚未得到评估。
评估直肠癌患者新辅助治疗后外周血免疫细胞的比例变化,并探讨肿瘤消退与调节性T(Treg)细胞之间的关系。
2018年1月至9月在山西省肿瘤医院接受术前新辅助治疗的直肠癌患者被纳入研究。通过流式细胞术检测新辅助治疗前后外周血中Treg、CD4+T、CD8+T、NK、B细胞及CD4+/CD8+比值。根据对新辅助治疗的反应,将患者分为降期组和对照组。
共纳入108例患者。新辅助治疗后Treg细胞比例显著降低(P < 0.05),但CD4 + T、CD8 + T、NK、B细胞及CD4 + /CD8 + 比值均未见变化(均P > 0.05)。降期组76例,对照组32例。降期组与对照组之间临床参数无显著差异(均P > 0.05)。新辅助治疗前,两组间免疫细胞比例无显著差异(均P > 0.05)。新辅助治疗后,降期组Treg、CD4 + T和B细胞均较治疗前显著降低(P < 0.05)。对照组新辅助治疗后CD4 + /CD8 + 比值降低(P < 0.05),而Treg和自然杀伤(NK)细胞比例未见变化。新辅助治疗后,与对照组相比,降期组Treg和B细胞较低,而CD4 + 及CD4 + /CD8 + 比值较高(P < 0.01)。
The efficacy of neoadjuvant therapy for rectal cancer has not been assessed.
To evaluate proportional changes in peripheral blood immune cells in rectal cancer patients after neoadjuvant therapy and assess the relationship between tumor regression and regulatory T (Treg) cells.
Rectal cancer patients who had received neoadjuvant therapy prior to surgery at Shanxi Cancer Hospital between January and September 2018 were enrolled in the study. Treg, CD4 + T, CD8 + T, NK, B cells, and CD4 + /CD8+ ratio in peripheral blood before and after neoadjuvant therapy were measured by flow cytometry. Patients were divided into down-staging and control groups, depending on their responses to neoadjuvant therapy.
A total of 108 patients were enrolled. The proportion of Treg cells was significantly lower after neoadjuvant therapy (P < 0.05) but no changes were seen in CD4 + T, CD8 + T, NK, B cells, or CD4 + /CD8 + ratio (all P > 0.05). There were 76 patients in the down-staging and 32 in the control groups. There were no significant differences in clinical parameters between down-staging and control groups (all P > 0.05). There were no significant differences in immune cell proportions between the two groups prior to neoadjuvant therapy (all P > 0.05). Treg, CD4 + T, and B cells were all significantly lower in the down-staging group after neoadjuvant therapy than before (P < 0.05). CD4 + /CD8 + ratios were lower (P < 0.05) while proportions of Treg and natural killer (NK) cells did not change after neoadjuvant therapy in the control group. Following neoadjuvant therapy, Treg and B cells were lower while CD4 + and CD4 + /CD8 + ratios were higher in the down-staging group compared to the control group (P < 0.01).
Treg cells may constitute a reference for judging the effect of neoadjuvant therapy in rectal cancer patients.
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