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肢端黑色素瘤浸润淋巴细胞的单细胞图谱揭示免疫抑制性肿瘤微环境

英文原题:Single-cell profiling of acral melanoma infiltrating lymphocytes reveals a suppressive tumor microenvironment.

PubMed 2024/12/04(内容时间) Sci Transl Med Q1 · IF 15.6(JCR 2025)

研究概要

我们的研究为提高ALM免疫治疗的疗效提供了基础。

中文摘要

肢端黑素瘤(ALM)是非高加索人群中最常见的黑素瘤亚型。尽管癌症免疫治疗取得了进展,但目前的免疫检查点抑制剂对ALM仍不理想。因此,我们通过对ALM中肿瘤浸润T淋巴细胞(TILs)的T细胞受体进行反应性筛选,并结合单细胞表型分析,开展了全面的免疫图谱分析。与皮肤黑素瘤相比,ALM显示出肿瘤反应性CD8细胞簇频率较低,并富集具有直接肿瘤识别能力的调节性T细胞,提示ALM中存在抑制性免疫微环境。肿瘤反应性CD8 TILs在具有治疗意义的亚群中表现出共抑制分子的异质性表达,包括KLRC1(NKG2A)。总体而言,我们的研究为提高ALM免疫治疗疗效提供了基础。

展开英文摘要原文

Acral lentiginous melanoma (ALM) is the most common melanoma subtype in non-Caucasians. Despite advances in cancer immunotherapy, current immune checkpoint inhibitors remain unsatisfactory for ALM. Hence, we conducted comprehensive immune profiling using single-cell phenotyping with reactivity screening of the T cell receptors of tumor-infiltrating T lymphocytes (TILs) in ALM. Compared with cutaneous melanoma, ALM showed a lower frequency of tumor-reactive CD8 clusters and an enrichment of regulatory T cells with direct tumor recognition ability, suggesting a suppressive immune microenvironment in ALM. Tumor-reactive CD8 TILs showed heterogeneous expression of coinhibitory molecules, including KLRC1 (NKG2A), in subpopulations with therapeutic implications. Overall, our study provides a foundation for enhancing the efficacy of immunotherapy in ALM.

论文信息

作者
Minowa T、Murata K、Mizue Y、Murai A、Nakatsugawa M、Sasaki K、Tokita S、Kubo T
单位
Department of Pathology, Sapporo Medical University School of Medicine, 060-8556 Sapporo, Hokkaido, Japan.Japan
文献类型
非美国政府资助研究
期刊
Science translational medicine2024 Dec 4
原文标识
PubMed 39630887 · DOI 10.1126/scitranslmed.adk8832