Department of Hematology, VU University Medical Center, Cancer Center Amsterdam, Amsterdam, The Netherlands.
Immunotherapy. 2013 Jun;5(6):621-37. doi: 10.2217/imt.13.51.
Myelodysplastic syndromes (MDS) are clonal disorders of the hematopoietic stem cell characterized by ineffective hematopoiesis leading to peripheral cytopenias. Different processes are involved in its pathogenesis, such as (epi)genetic alterations and immunological dysfunctions. The nature of immune dysregulation is markedly different between various MDS risk groups. In low-risk MDS, the immune system is in a proinflammatory state, whereas in high-risk disease, immunosuppressive features facilitate expansion of the dysplastic clone and can eventually lead to disease progression to acute myeloid leukemia. Various cell types contribute to dysregulation of immune responses in MDS. Dendritic cells (DCs) are important regulators of immunity. However, the role of DCs in MDS has yet to be elucidated. It has been suggested that impaired DC function can hamper adequate immune responses. This review focuses on the involvement of DCs in immune dysregulation in low- and high-risk MDS and the implications for DC-targeted therapies.
骨髓增生异常综合征(MDS)是一种造血干细胞克隆性疾病,其特征为无效造血导致外周血细胞减少。不同的过程参与其发病机制,如(表观)遗传改变和免疫功能障碍。在不同的 MDS 风险组中,免疫失调的性质明显不同。在低危 MDS 中,免疫系统处于促炎状态,而在高危疾病中,免疫抑制特征促进了异常克隆的扩增,并最终导致疾病进展为急性髓系白血病。各种细胞类型有助于 MDS 中免疫反应的失调。树突状细胞(DC)是免疫的重要调节剂。然而,DC 在 MDS 中的作用尚未阐明。有人认为,DC 功能受损会阻碍适当的免疫反应。本综述重点介绍了 DC 在低危和高危 MDS 免疫失调中的作用,以及针对 DC 的治疗的意义。