Institute of Dermatology, Azienda Sanitaria Universitaria Friuli Centrale (ASUFC), 33100 Udine, Italy.
Dipartimento di Scienze Mediche e Chirurgiche, University of Bologna, 40138 Bologna, Italy.
Cells. 2024 Mar 28;13(7):584. doi: 10.3390/cells13070584.
Cutaneous T cell lymphomas (CTCLs), encompassing mycosis fungoides (MF) and Sézary syndrome (SS), present a complex landscape influenced by cytokines and cellular responses. In this work, the intricate relationship between these inflammatory proteins and disease pathogenesis is examined, focusing on what is known at the clinical and therapeutic levels regarding the most well-known inflammatory mediators. An in-depth look is given to their possible alterations caused by novel immunomodulatory drugs and how they may alter disease progression. From this narrative review of the actual scientific landscape, Interferon-gamma (IFN-γ) emerges as a central player, demonstrating a dual role in both promoting and inhibiting cancer immunity, but the work navigates through all the major interleukins known in inflammatory environments. Immunotherapeutic perspectives are elucidated, highlighting the crucial role of the cutaneous microenvironment in shaping dysfunctional cell trafficking, antitumor immunity, and angiogenesis in MF, showcasing advancements in understanding and targeting the immune phenotype in CTCL. In summary, this manuscript aims to comprehensively explore the multifaceted aspects of CTCL, from the immunopathogenesis and cytokine dynamics centred around TNF-α and IFN-γ to evolving therapeutic modalities. Including all the major known and studied cytokines in this analysis broadens our understanding of the intricate interplay influencing CTCL, paving the way for improved management of this complex lymphoma.
皮肤 T 细胞淋巴瘤(CTCLs)包括蕈样真菌病(MF)和赛泽里综合征(SS),受细胞因子和细胞反应的影响,呈现出复杂的局面。在这项工作中,研究了这些炎症蛋白与疾病发病机制之间的复杂关系,重点关注在临床和治疗水平上已知的最著名的炎症介质。深入探讨了新型免疫调节药物可能引起的变化,以及它们如何改变疾病进展。通过对实际科学领域的叙述性综述,干扰素-γ(IFN-γ)作为一个核心分子出现,在促进和抑制癌症免疫方面表现出双重作用,但这项工作也涵盖了炎症环境中所有已知的主要白细胞介素。还阐述了免疫治疗的观点,强调了皮肤微环境在塑造 MF 中功能失调的细胞迁移、抗肿瘤免疫和血管生成方面的关键作用,展示了在理解和靶向 CTCL 免疫表型方面的进展。总之,本手稿旨在全面探讨 CTCL 的多方面,从以 TNF-α和 IFN-γ为中心的免疫发病机制和细胞因子动力学,到不断发展的治疗方式。在这项分析中包含所有主要的已知和研究的细胞因子,拓宽了我们对影响 CTCL 的复杂相互作用的理解,为改善这种复杂淋巴瘤的管理铺平了道路。