Giannoni Paolo, Marini Cecilia, Cutrona Giovanna, Sambuceti Gian Mario, Fais Franco, de Totero Daniela
Department of Experimental Medicine, Biology Section, University of Genova, 16132 Genova, Italy.
Nuclear Medicine Unit, IRCCS Ospedale Policlinico San Martino, 16132 Genova, Italy.
Cancers (Basel). 2023 Oct 19;15(20):5058. doi: 10.3390/cancers15205058.
Chronic lymphocytic leukemia (CLL) is the most frequent leukemia in Western countries. Although characterized by the progressive expansion and accumulation of leukemic B cells in peripheral blood, CLL cells develop in protective niches mainly located within lymph nodes and bone marrow. Multiple interactions between CLL and microenvironmental cells may favor the expansion of a B cell clone, further driving immune cells toward an immunosuppressive phenotype. Here, we summarize the current understanding of bone tissue alterations in CLL patients, further addressing and suggesting how the multiple interactions between CLL cells and osteoblasts/osteoclasts can be involved in these processes. Recent findings proposing the disruption of the endosteal niche by the expansion of a leukemic B cell clone appear to be a novel field of research to be deeply investigated and potentially relevant to provide new therapeutic approaches.
慢性淋巴细胞白血病(CLL)是西方国家最常见的白血病。尽管其特征是外周血中白血病性B细胞进行性扩增和积聚,但CLL细胞在主要位于淋巴结和骨髓内的保护性微环境中发育。CLL与微环境细胞之间的多种相互作用可能有利于B细胞克隆的扩增,进一步促使免疫细胞向免疫抑制表型发展。在此,我们总结了目前对CLL患者骨组织改变的认识,进一步探讨并提出CLL细胞与成骨细胞/破骨细胞之间的多种相互作用如何参与这些过程。最近的研究结果表明,白血病性B细胞克隆的扩增破坏了骨内膜微环境,这似乎是一个有待深入研究的新领域,可能与提供新的治疗方法相关。