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骨髓增生异常综合征中的免疫机制

Immune Mechanisms in Myelodysplastic Syndrome.

作者信息

Glenthøj Andreas, Ørskov Andreas Due, Hansen Jakob Werner, Hadrup Sine Reker, O'Connell Casey, Grønbæk Kirsten

机构信息

Epi-/Genome Laboratory, Department of Hematology, Rigshospitalet, Copenhagen University Hospital, Copenhagen 2100, Denmark.

Section for Immunology and Vaccinology, National Veterinary Institute, Technical University of Denmark, Frederiksberg 1870, Denmark.

出版信息

Int J Mol Sci. 2016 Jun 15;17(6):944. doi: 10.3390/ijms17060944.

Abstract

Myelodysplastic syndrome (MDS) is a spectrum of diseases, characterized by debilitating cytopenias and a propensity of developing acute myeloid leukemia. Comprehensive sequencing efforts have revealed a range of mutations characteristic, but not specific, of MDS. Epidemiologically, autoimmune diseases are common in patients with MDS, fueling hypotheses of common etiological mechanisms. Both innate and adaptive immune pathways are overly active in the hematopoietic niche of MDS. Although supportive care, growth factors, and hypomethylating agents are the mainstay of MDS treatment, some patients-especially younger low-risk patients with HLA-DR15 tissue type-demonstrate impressive response rates after immunosuppressive therapy. This is in contrast to higher-risk MDS patients, where several immune activating treatments, such as immune checkpoint inhibitors, are in the pipeline. Thus, the dual role of immune mechanisms in MDS is challenging, and rigorous translational studies are needed to establish the value of immune manipulation as a treatment of MDS.

摘要

骨髓增生异常综合征(MDS)是一系列疾病,其特征为血细胞减少导致身体虚弱,且有发展为急性髓系白血病的倾向。全面的测序研究揭示了一系列MDS特有的但并非特异性的突变。从流行病学角度看,自身免疫性疾病在MDS患者中很常见,这引发了关于共同病因机制的假说。先天性和适应性免疫途径在MDS的造血微环境中均过度活跃。尽管支持性治疗、生长因子和去甲基化药物是MDS治疗的主要手段,但一些患者——尤其是年轻的具有HLA - DR15组织类型的低风险患者——在接受免疫抑制治疗后显示出令人印象深刻的缓解率。这与高风险MDS患者形成对比,目前有几种免疫激活治疗方法,如免疫检查点抑制剂,正在研发中。因此,免疫机制在MDS中的双重作用具有挑战性,需要进行严格的转化研究来确定免疫调控作为MDS治疗方法的价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7fa/4926477/341db94fc82e/ijms-17-00944-g001.jpg

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