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.
肿瘤细胞治疗研究
英文原题:Tumour Infiltrating Lymphocytes (TILs) and immune composition in breast cancer patients from Kenya: Spatial distributions and associations with risk factors and tumour characteristics.
Tumour Infiltrating Lymphocytes (TILs) and immune composition in breast cancer patients from Kenya: Spatial distributions and associations with risk factors and tumour characteristics.
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侵袭性更强的 BC 中 TIL 富集情况与既往在其他人群中发表的数据相似。
撒哈拉以南非洲乳腺癌患者的免疫特征研究不足。本研究描述肯尼亚女性肿瘤内间质TIL(sTIL)和浸润前缘间质TIL(LE-TIL)的分布,并按乳腺癌亚型分析TIL与风险因素和临床特征的关系。
依据国际TIL工作组指南,对经病理确诊的乳腺癌HE切片进行视觉定量;制作组织芯片并以免疫组化检测CD3、CD4、CD8、CD68、CD20和FOXP3。通过线性及逻辑回归评估风险因素、肿瘤特征与标志物及总TIL的关系,并调整协变量。
纳入226例浸润性乳腺癌。LE-TIL平均比例为27.9%,显著高于sTIL的13.5%。两类区域的TIL主要由CD3、CD8和CD68细胞构成。TIL较高与Ki-67高表达、高分级及侵袭性亚型相关,但关联因空间位置而异。初潮年龄较晚(≥15岁)与肿瘤内间质CD3增加相关(OR 2.06,95% CI 1.26–3.37)。
侵袭性乳腺癌中TIL富集与其他人群报告相似。sTIL和LE-TIL与多数因素的关联不同,凸显未来研究评估TIL空间分布的重要性。
The immune landscape of breast cancer (BC) in patients from Sub Saharan Africa is understudied. Our aims were to describe the distribution of Tumour Infiltrating Lymphocytes (TILs) within the intratumoural stroma (sTILs) and the leading/invasive edge stroma (LE-TILs), and to evaluate TILs across BC subtypes with established risk factors and clinical characteristics in Kenyan women.
Visual quantification of sTILs and LE-TILs were performed on Haematoxylin and eosin -stained pathologically confirmed BC cases based on the International TIL working group guidelines. Tissue Microarrays were constructed and stained with immunohistochemistry (IHC) for CD3, CD4, CD8, CD68, CD20, and FOXP3. Linear and logistic regression models were used to assess associations between risk factors and tumour features with IHC markers and total TILs, after adjusting for other covariates.
A total of 226 invasive BC cases were included. Overall, LE-TIL (mean = 27.9, SD = 24.5) proportions were significantly higher than sTIL (mean = 13.5, SD = 15.8). Both sTILs and LE- TILs were predominantly composed of CD3, CD8, and CD68. We found higher TILs to be associated with high KI67/high grade and aggressive tumour subtypes, although these associations varied by TIL locations. Older age at menarche ( 15 vs. < 15 years) was associated with higher CD3 (OR: 2.06, 95%CI:1.26-3.37), but only for the intra-tumour stroma.
The TIL enrichment in more aggressive BCs is similar to previously published data in other populations. The distinct associations of sTIL/LE-TIL measures with most examined factors highlight the importance of spatial TIL evaluations in future studies.
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