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慢性淋巴细胞白血病的病理生理学与人类 B1 细胞的发育。

Pathophysiology of chronic lymphocytic leukemia and human B1 cell development.

机构信息

Department of Medicine and Biosystemic Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-Ku, Fukuoka, 812-8582, Japan.

出版信息

Int J Hematol. 2020 May;111(5):634-641. doi: 10.1007/s12185-019-02788-7. Epub 2019 Dec 3.

Abstract

Chronic lymphocytic leukemia (CLL), the most frequent type of leukemia in adults, is a lymphoproliferative disease characterized by the clonal expansion of mature CD5 B cells in peripheral blood, bone marrow, and secondary lymphoid tissues. Over the past decade, substantial advances have been made in understanding the pathogenesis of CLL, including the identification of recurrent mutations, and clarification of clonal architectures, transcriptome analyses, and the multistep leukemogenic process. The biology of CLL is now better understood. The present review focuses on recent insights into CLL leukemogenesis, emphasizing the role of genetic lesions, and the multistep process initiating from very immature hematopoietic stem cells. Finally, we also review progress in the study of human B1 B cells, the putative normal counterparts of CLL cells.

摘要

慢性淋巴细胞白血病(CLL)是成人中最常见的白血病类型,是一种淋巴增殖性疾病,其特征是外周血、骨髓和次级淋巴组织中成熟 CD5+B 细胞的克隆性扩张。在过去的十年中,人们在理解 CLL 的发病机制方面取得了重大进展,包括反复出现的突变的鉴定,克隆结构、转录组分析和多步骤白血病发生过程的阐明。现在对 CLL 的生物学有了更好的理解。本综述重点介绍了 CLL 白血病发生的最新见解,强调了遗传病变的作用,以及从非常不成熟的造血干细胞开始的多步骤过程。最后,我们还回顾了人类 B1 B 细胞研究的进展,B1 B 细胞是 CLL 细胞的假定正常对应物。

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