Department of Dermatology and Venereology, Peking University First Hospital, No.8 Xishiku Street, Xi Cheng District, Beijing 100034, China.
Acta Derm Venereol. 2021 Dec 7;101(12):adv00613. doi: 10.2340/actadv.v101.570.
Cutaneous T cell lymphoma is a generally indolent disease derived from skin-homing mature T cells. However, in advanced stages, cutaneous T cell lymphoma may manifest aggressive clinical behaviour and lead to a poor prognosis. The mechanism of disease progression in cutaneous T cell lymphoma remains unknown. This study, based on a large clinical cohort, found that IKZF2, an essential transcription factor during T cell development and differentiation, showed stage- dependent overexpression in the malignant T cells in mycosis fungoides lesions. IKZF2 is specifically over- expressed in advanced-stage mycosis fungoides lesions, and correlates with poor prognosis. Mechanistically, overexpression of IKZF2 promotes cutaneous T cell lymphoma progression via inhibiting malignant cell apoptosis and may contribute to tumour immune escape by downregulating major histocompatibility complex II molecules and up-regulating the production of anti-inflammatory cytokine interleukin-10 by malignant T cells. These results demonstrate the important role of IKZF2 in high-risk cutaneous T cell lymphoma and pave the way for future targeted therapy.
皮肤 T 细胞淋巴瘤是一种源自皮肤归巢成熟 T 细胞的惰性疾病。然而,在晚期,皮肤 T 细胞淋巴瘤可能表现出侵袭性的临床行为,并导致预后不良。皮肤 T 细胞淋巴瘤的疾病进展机制尚不清楚。本研究基于一个大型临床队列,发现 IKZF2 是 T 细胞发育和分化过程中的一个必需转录因子,在蕈样肉芽肿病变中的恶性 T 细胞中表现出阶段依赖性过表达。IKZF2 在晚期蕈样肉芽肿病变中特异性过表达,并与预后不良相关。从机制上讲,IKZF2 的过表达通过抑制恶性细胞凋亡促进皮肤 T 细胞淋巴瘤的进展,并可能通过下调主要组织相容性复合体 II 分子和上调恶性 T 细胞产生抗炎细胞因子白细胞介素 10 来促进肿瘤免疫逃逸。这些结果表明 IKZF2 在高危皮肤 T 细胞淋巴瘤中的重要作用,并为未来的靶向治疗铺平了道路。