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肾脏混合性上皮间质瘤中肿瘤浸润淋巴细胞的模式:五例病例回顾。

Pattern of Tumor-Infiltrating Lymphocytes in Mixed Epithelial and Stromal Tumor of the Kidney: A Review of Five Cases.

机构信息

Department of Urology, Center for Urological Cancer, National Cancer Center, Goyang 10408, Korea.

Department of Pathology and Translational Genomics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 06351, Korea.

出版信息

Cells. 2021 Apr 16;10(4):917. doi: 10.3390/cells10040917.

Abstract

Mixed epithelial and stromal tumor of the kidney (MESTK), a benign rare tumor with malignant transformation potential, is thought to be derived from fetal or immature cells originating from the mesonephric and Müllerian ducts. However, due to its rarity, little is known about the anti-tumor immune responses in MESTK. Herein, we present five cases of MESTK and evaluate the population of tumor-infiltrating lymphocytes (TILs) using a freshly obtained MESTK sample. Microscopically, TILs were scattered or clustered in large aggregates in the stroma in all five cases; furthermore, three cases exhibited heavy, large lymphocytic aggregates with no well-organized tertiary lymphoid structures with germinal centers. Flow cytometric analysis of TILs in one freshly obtained MESTK sample revealed that >40% of CD3 T cells were effector memory FasCD28 γδ T cells expressing high levels of programmed cell death protein 1 and inducible T-cell co-stimulator, but low levels of CD44 and CD27. Most αß T cells exhibited a naïve phenotype. Additionally, we detected many activated class-switched CD21CD27 B cells as well as CD11cIgM marginal zone B-like and CD27CD21CD23 immunoglobulin (Ig)DIgM age-associated B-like cells. Collectively, for the first time, we report the immune microenvironment pattern of MESTK to oncogenic stress.

摘要

肾混合性上皮间质肿瘤(MESTK)是一种具有恶性转化潜能的良性罕见肿瘤,被认为来源于中肾和 Müllerian 管的胎儿或未成熟细胞。然而,由于其罕见性,对于 MESTK 中的抗肿瘤免疫反应知之甚少。在此,我们报告了 5 例 MESTK 病例,并使用新鲜获得的 MESTK 样本评估了肿瘤浸润淋巴细胞(TIL)的群体。在所有 5 例中,显微镜下 TIL 均散布或聚集成大块在基质中;此外,3 例表现为大量淋巴细胞聚集,无成熟的三级淋巴样结构和生发中心。对一个新鲜获得的 MESTK 样本中 TIL 的流式细胞分析显示,>40%的 CD3 T 细胞是效应记忆 FasCD28 γδ T 细胞,表达高水平的程序性细胞死亡蛋白 1 和诱导型 T 细胞共刺激分子,但低水平表达 CD44 和 CD27。大多数 αß T 细胞表现为幼稚表型。此外,我们还检测到许多活化的类别转换 CD21CD27 B 细胞以及 CD11cIgM 边缘区 B 样细胞和 CD27CD21CD23 免疫球蛋白(Ig)DIgM 年龄相关 B 样细胞。总之,我们首次报告了 MESTK 对致癌应激的免疫微环境模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88b5/8074008/b6f887c48177/cells-10-00917-g001.jpg

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