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 use of natural killer cell activity and PPD test in the prediction of results in intravesical BCG treatment of patients with nonmuscle-invasive bladder cancer.
The use of natural killer cell activity and PPD test in the prediction of results in intravesical BCG treatment of patients with nonmuscle-invasive bladder cancer.
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我们得出结论,在 NMIBC 患者开始膀胱内 BCG 治疗前进行的 PPD 试验和 NK 活性检测结果,可能是一个可用于预测治疗期间复发风险的标志物。
通过使用细胞免疫反应的组成部分,如结核菌素皮肤试验(PPD)和自然杀伤(NK)活性测定,预测非肌层浸润性膀胱肿瘤(NIBC)患者膀胱内BCG治疗的疗效。
99例因NMIBC开始接受膀胱内BCG治疗的患者被前瞻性评估。纳入根据EAU NMIBC评分系统属于中危、高危和极高危组且既往从未接受过膀胱内BCG治疗的患者。记录患者的临床和人口学特征(年龄、性别、EAU NMIBC风险组、EORTC进展和复发评分、CUETO进展和复发评分、合并症的存在及类型)。在开始膀胱内BCG治疗前3天测量NK活性并实施PPD试验。PPD结果在试验后72小时以毫米为单位测量。
BCG治疗前测量的PPD值作为独立变量,在复发患者中显著较低。当cutoff值为200-500 pg/dl时,BCG治疗前获得的NK活性结果与治疗后复发之间存在显著相关性。复发时间与PPD和NKA测量值之间无显著关系。
To predict the efficacy of intravesical BCG therapy in patients with nonmuscle-invasive bladder tumors (NIBC) by using components of the cellular immune response such as the tuberculin skin test (PPD) and natural killer (NK) activity measurement.
Ninety-nine patients who were started on intravesical BCG therapy for NIBC were evaluated prospectively. Patients who were included in the intermediate, high, and very high-risk groups according to the EAU NMIBC Scoring System and who had never received intravesical BCG therapy previously were included. The clinical and demographic characteristics of the patients (age, gender, EAU NMBIC risk group, EORTC progression and recurrence scores, CUETO progression and recurrence scores, presence and types of comorbidity) were recorded. NK activity was measured and the PPD test was applied 3 days before the start of intravesical BCG therapy. The results of PPD were measured in millimeters 72 h after the test.
PPD values measured before BCG treatment, as an independent variable, were found to be significantly lower in patients with recurrence. A significant correlation was detected between NK activity results obtained before BCG treatment and recurrence after treatment, when the cutoff was 200-500 pg/dl. There was no significant relationship between the time to recurrence and PPD and NKA measurements.
We conclude that the results of PPD test and NK activity measurement performed before starting intravesical BCG therapy in NIBC may be a marker that can be used to predict the risk of recurrence under treatment.
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