Division of Hematology, Department Patologia Umana dell'Adulto e dell'Età Evolutiva, University of Messina, Località Gazzi, Via Consolare Valeria, Messina, Italy.
Institute of Applied Sciences and Intelligent Systems "Eduardo Caianiello" (ISASI)-National Research Council of Italy (CNR), Messina Unit, Via Torre Bianca, Messina, Italy.
Mediators Inflamm. 2017;2017:1852517. doi: 10.1155/2017/1852517. Epub 2017 Sep 26.
Multiple myeloma (MM) is typically exemplified by a desynchronized cytokine system with increased levels of inflammatory cytokines. We focused on the contrast between inflammatory and anti-inflammatory systems by assessing the role of cytokines and their influence on MM. The aim of this review is to summarize the available information to date concerning this equilibrium to provide an overview of the research exploring the roles of serum cytokines in MM. However, the association between MM and inflammatory cytokines appears to be inadequate, and other functions, such as pro-proliferative or antiproliferative effects, can assume the role of cytokines in the genesis and progression of MM. It is possible that inflammation, when guided by cancer-specific Th1 cells, may inhibit tumour onset and progression. In a Th1 microenvironment, proinflammatory cytokines (e.g., IL-6 and IL-1) may contribute to tumour eradication by attracting leucocytes from the circulation and by increasing CD4 T cell activity. Hence, caution should be used when considering therapies that target factors with pro- or anti-inflammatory activity. Drugs that may reduce the tumour-suppressive Th1-driven inflammatory immune response should be avoided. A better understanding of the relationship between inflammation and myeloma will ensure more effective therapeutic interventions.
多发性骨髓瘤(MM)通常表现为细胞因子系统失调,炎症细胞因子水平升高。我们通过评估细胞因子的作用及其对 MM 的影响,关注炎症和抗炎系统之间的差异。本综述的目的是总结迄今为止关于这种平衡的现有信息,概述探索血清细胞因子在 MM 中的作用的研究。然而,MM 与炎症细胞因子之间的关联似乎并不充分,其他功能,如促有丝分裂或抗有丝分裂作用,可能会在 MM 的发生和进展中扮演细胞因子的角色。当炎症受到癌症特异性 Th1 细胞的控制时,可能会抑制肿瘤的发生和进展。在 Th1 微环境中,促炎细胞因子(如 IL-6 和 IL-1)通过吸引循环中的白细胞和增加 CD4 T 细胞的活性,可能有助于肿瘤的清除。因此,在考虑针对具有促炎或抗炎活性的因素的治疗时应谨慎。应避免使用可能降低肿瘤抑制性 Th1 驱动的炎症免疫反应的药物。更好地了解炎症和骨髓瘤之间的关系将确保更有效的治疗干预。