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 Fas+CD28− 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 CD21+CD27+ B cells as well as CD11chighIgMhigh marginal zone B-like and CD27−CD21−CD23− immunoglobulin (Ig)DhighIgMlow age-associated B-like cells. Collectively, for the first time, we report the immune microenvironment pattern of MESTK to oncogenic stress.

Highlights

  • Mixed epithelial and stromal tumor of the kidney (MESTK) is a unique renal neoplasm characterized by epithelial and stromal proliferation with variable cellularity and growth patterns [1,2,3,4]

  • As little is known about the antitumor immune response against MESTK compared with other malignancies of the kidney, we reviewed the immunopathologic characteristics of MESTK in five patients with this tumor and performed an in-depth analysis of the phenotype of tumor-infiltrating lymphocytes (TILs) using a freshly obtained

  • This study demonstrated an association among the tumor-associated macrophage phenotype, regulatory T cells, and immunosuppressed CD8+ T cells

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Summary

Kalyuzhny

Department of Pathology and Translational Genomics, Samsung Medical Center, Sungkyunkwan University Department of Urology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 06351, Korea These authors contributed equally to this work.

Introduction
Patients and Samples
Immunohistochemistry
Flow Cytometric Analysis
Results
Flow Cytometric Analysis of Intratumor Lymphocytes
Discussion
Full Text
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