基于 DNA 超分子水凝胶的保护性 NK 细胞储库用于增强三阴性乳腺癌治疗
Protective NK Cell Reservoir Based on DNA Supramolecular Hydrogel for Enhanced Triple-Negative Breast Cancer Therapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:High platelet-to-lymphocyte ratios in triple-negative breast cancer associates with immunosuppressive status of TILs.
High platelet-to-lymphocyte ratios in triple-negative breast cancer associates with immunosuppressive status of TILs.
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我们的数据表明,PLR 与 TIL 评估相结合可能有助于更准确地预测 TNBC 患者的结局。
TIL(肿瘤浸润淋巴细胞)(TILs)是乳腺癌的预后标志物,TIL高浸润与患者更好的预后相关。同时,外周血中涉及免疫细胞的参数也已被确立为预后标志物。高血小板与淋巴细胞比值(PLR)和中性粒细胞与淋巴细胞比值(NLR)与乳腺癌不良预后相关,但其机制仍不清楚。迄今为止,TILs和这些参数一直是分别进行研究的。
我们研究了502例未接受术前化疗的浸润性乳腺癌患者的手术标本中,TILs与同一患者外周血标志物PLR和NLR之间的关系。为了分析三阴性乳腺癌(TNBC)患者的结局,还检查了59例接受术前化疗的患者。为了进行免疫细胞谱分析,对CD3、CD4、CD8、FOXP3和T-bet进行了多重荧光免疫组化(mfIHC)。
在TNBC中观察到PLR与TIL呈正相关(P = 0.013)。在mfIHC上,高PLR和高NLR患者的肿瘤含有更多CD3 + CD4 + FOXP3 + T细胞(分别为P = 0.049和0.019),而在CD8 + T细胞中未观察到趋势。TNBC患者根据TIL和PLR表现出不同的结局模式,TIL高/PLR低组的疾病复发率和死亡率最低,无远处转移生存期和总生存期最长,而TIL低/PLR高组的生存期最短。
Rating lymphocytes (TILs) are a prognostic marker in breast cancer and high TIL infiltration correlates with better patient outcomes. Meanwhile, parameters involving immune cells in peripheral blood have also been established as prognostic markers. High platelet-to-lymphocyte ratios (PLRs) and neutrophil-to-lymphocyte ratios (NLRs) are related to poor outcomes in breast cancer, but their mechanisms remain unknown. To date, TILs and these parameters have been examined separately.
We investigated the relationship between TILs and the peripheral blood markers, PLR and NLR, in the same patients, using surgical specimens from 502 patients with invasive breast carcinoma without preoperative chemotherapy. For analysis of triple-negative breast cancer (TNBC) patient outcomes, 59 patients who received preoperative chemotherapy were also examined. For immune cell profiling, multiplexed fluorescent immunohistochemistry (mfIHC) of CD3, CD4, CD8, FOXP3 and T-bet, was conducted.
A positive correlation between PLR and TIL was observed in TNBC (P = 0.013). On mfIHC, tumors in patients with high PLR and NLR contained more CD3 + CD4 + FOXP3 + T-cells (P = 0.049 and 0.019, respectively), while no trend was observed in CD8 + T-cells. TNBC patients had different patterns of outcomes according to TIL and PLR, with the TIL-high/PLR-low group having the lowest rate of disease relapse and death, and the longest distant metastasis-free and overall survivals, while the TIL-low/PLR-high group had the shortest survivals.
Our data suggest that the combination of PLR with TIL assessment may enable more accurate prediction of patient outcomes with TNBC.
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