Kwantwi Louis Boafo, Rosen Steven T, Querfeld Christiane
Department of Pathology, City of Hope Medical Center, Duarte, CA 91010, USA.
Beckman Research Institute, Duarte, CA 91010, USA.
Cancers (Basel). 2024 Oct 1;16(19):3368. doi: 10.3390/cancers16193368.
Cutaneous T cell lymphomas (CTCLs) are a heterogeneous group of non-Hodgkin lymphomas, with mycosis fungoides and Sézary syndrome being the two common subtypes. Despite the substantial improvement in early-stage diagnosis and treatments, some patients still progress to the advanced stage with an elusive underpinning mechanism. While this unsubstantiated disease mechanism coupled with diverse clinical outcomes poses challenges in disease management, emerging evidence has implicated the tumor microenvironment in the disease process, thus revealing a promising therapeutic potential of targeting the tumor microenvironment. Notably, malignant T cells can shape their microenvironment to dampen antitumor immunity, leading to Th2-dominated responses that promote tumor progression. This is largely orchestrated by alterations in cytokines expression patterns, genetic dysregulations, inhibitory effects of immune checkpoint molecules, and immunosuppressive cells. Herein, the recent insights into the determining factors in the CTCL tumor microenvironment that support their progression have been highlighted. Also, recent advances in strategies to target the CTCL tumor micromovement with the rationale of improving treatment efficacy have been discussed.
皮肤T细胞淋巴瘤(CTCL)是一组异质性非霍奇金淋巴瘤,蕈样肉芽肿和塞扎里综合征是两种常见亚型。尽管早期诊断和治疗有了显著改善,但仍有一些患者进展到晚期,其潜在机制难以捉摸。虽然这种未经证实的疾病机制以及多样的临床结果给疾病管理带来了挑战,但新出现的证据表明肿瘤微环境参与了疾病过程,从而揭示了靶向肿瘤微环境的潜在治疗前景。值得注意的是,恶性T细胞可以塑造其微环境以抑制抗肿瘤免疫,导致以Th2为主导的反应,促进肿瘤进展。这在很大程度上是由细胞因子表达模式的改变、基因失调、免疫检查点分子的抑制作用和免疫抑制细胞所协调的。在此,重点介绍了对支持CTCL进展的肿瘤微环境决定因素的最新见解。此外,还讨论了以提高治疗效果为目标靶向CTCL肿瘤微环境的策略的最新进展。