Krejsgaard Thorbjørn, Lindahl Lise M, Mongan Nigel P, Wasik Mariusz A, Litvinov Ivan V, Iversen Lars, Langhoff Erik, Woetmann Anders, Odum Niels
Department of Immunology and Microbiology, University of Copenhagen, Blegdamsvej 3c, DK-2200, Copenhagen N, Denmark.
Department of Dermatology, Aarhus University Hospital, Aarhus, Denmark.
Semin Immunopathol. 2017 Apr;39(3):269-282. doi: 10.1007/s00281-016-0594-9. Epub 2016 Oct 7.
Cutaneous T-cell lymphomas (CTCL) are characterized by the presence of chronically inflamed skin lesions containing malignant T cells. Early disease presents as limited skin patches or plaques and exhibits an indolent behavior. For many patients, the disease never progresses beyond this stage, but in approximately one third of patients, the disease becomes progressive, and the skin lesions start to expand and evolve. Eventually, overt tumors develop and the malignant T cells may disseminate to the blood, lymph nodes, bone marrow, and visceral organs, often with a fatal outcome. The transition from early indolent to progressive and advanced disease is accompanied by a significant shift in the nature of the tumor-associated inflammation. This shift does not appear to be an epiphenomenon but rather a critical step in disease progression. Emerging evidence supports that the malignant T cells take control of the inflammatory environment, suppressing cellular immunity and anti-tumor responses while promoting a chronic inflammatory milieu that fuels their own expansion. Here, we review the inflammatory changes associated with disease progression in CTCL and point to their wider relevance in other cancer contexts. We further define the term "malignant inflammation" as a pro-tumorigenic inflammatory environment orchestrated by the tumor cells and discuss some of the mechanisms driving the development of malignant inflammation in CTCL.
皮肤T细胞淋巴瘤(CTCL)的特征是存在含有恶性T细胞的慢性炎症性皮肤病变。早期疾病表现为局限性皮肤斑块或斑片,呈惰性病程。对许多患者来说,疾病从未进展到这个阶段之后,但在大约三分之一的患者中,疾病会进展,皮肤病变开始扩大和演变。最终,明显的肿瘤形成,恶性T细胞可能扩散到血液、淋巴结、骨髓和内脏器官,常常导致致命后果。从早期惰性疾病到进展期和晚期疾病的转变伴随着肿瘤相关炎症性质的显著变化。这种转变似乎不是一种附带现象,而是疾病进展中的关键一步。新出现的证据支持恶性T细胞控制炎症环境,抑制细胞免疫和抗肿瘤反应,同时促进一种慢性炎症环境,从而推动自身的增殖。在此,我们综述与CTCL疾病进展相关的炎症变化,并指出它们在其他癌症背景下的更广泛相关性。我们进一步将“恶性炎症”定义为由肿瘤细胞精心策划的促肿瘤炎症环境,并讨论一些驱动CTCL中恶性炎症发展的机制。