冷凝集素病:一种独特的骨髓克隆性b细胞增生性疾病

IF 0.9 Q4 HEMATOLOGY
Hemato Pub Date : 2022-02-13 DOI:10.3390/hemato3010014
F. Climent, J. Cid, A. Sureda
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引用次数: 1

摘要

冷凝集素病(CAD)是一种以骨髓克隆性b细胞增生性疾病为特征的独特临床病理实体。b细胞基因突变影响NF-ΚB以及染色质修饰和重塑途径。B细胞产生的克隆免疫球蛋白在低温下与红细胞结合,引起红细胞聚集、补体级联激活和冷自身抗体自身免疫性溶血性贫血(cAIHA)。临床表现为感冒引起的症状和cAIHA。治疗方案包括“等待和观察”、以利妥昔单抗为基础的方案和补充导向的治疗。类固醇不能用于治疗冠心病。在最近的分子研究之后,可能会发现新的靶向治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cold Agglutinin Disease: A Distinct Clonal B-Cell Lymphoproliferative Disorder of the Bone Marrow
Cold agglutinin disease (CAD) is a distinct clinicopathologic entity characterized by clonal B-cell lymphoproliferative disorder in the bone marrow. B-cell gene mutations affect NF-ΚB as well as chromatin modification and remodeling pathways. Clonal immunoglobulins produced by B cells bind to red cells (RBCs) at cold temperatures causing RBC aggregation, complement cascade activation and cold-autoantibody autoimmune hemolytic anemia (cAIHA). The clinical picture shows cold-induced symptoms and cAIHA. Therapeutic options include “wait and watch”, rituximab-based regimens, and complement-directed therapies. Steroids must not be used for treating CAD. New targeted therapies are possibly identified after recent molecular studies.
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来源期刊
CiteScore
1.30
自引率
0.00%
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审稿时长
11 weeks
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