MDS的免疫失调:细胞因子和免疫细胞的作用

Selma Z D'silva, S. Rajadhyaksha, Meenakshi Singh
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引用次数: 4

摘要

骨髓增生异常综合征(MDS)是一种影响60岁以上个体的造血干细胞疾病。其特点是造血功能低下,造血细胞大量凋亡。MDS患者转化为急性髓系白血病的风险很高。MDS细胞凋亡和逃避免疫监视的主要原因是由多种因素引起的免疫失调,如细胞因子产生异常和各种免疫细胞的影响。在过去的十年中,各种促炎细胞因子和许多免疫细胞,如自然杀伤细胞、调节性T细胞、细胞毒性T细胞、间充质干细胞、髓源性抑制细胞和树突状细胞,都与导致MDS发病的免疫失调有关。在这篇综述中,我们主要关注这些免疫因子作用的现有数据。
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Immune Dysregulation in MDS: The Role of Cytokines and Immune Cells
Myelodysplastic syndrome (MDS) is a hematopoietic stem cell disorder affecting individuals over the age of 60 years. It is characterized by ineffective hematopoiesis and extensive apoptosis of hematopoietic cells. MDS patients are at a high risk of transforming in to acute myeloid leukemia. The main cause of apoptosis and escape from immune surveillance in MDS is immune dysregulation caused by a number of factors such as aberrant cytokine production and influence of various immune cells. In the past decade various pro-inflammatory cytokines and a number of immune cells such as Natural Killer cells, regulatory T cells, cytotoxic T cells, mesenchymal stem cells, myeloid derived suppressor cells and dendritic cells have been implicated in immune dysregulation leading to MDS pathogenesis. In this review we focus on the current data available on the role of these immune factors.
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Diagnosis and Classification of Myelodysplastic Syndrome Introductory Chapter: Progress in Myelodysplastic Syndrome Area Immune Dysregulation in MDS: The Role of Cytokines and Immune Cells Myelodysplastic Syndromes: An Update on Pathophysiology and Management Noncoding RNAs in Myelodysplastic Syndromes
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