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CD99 抗体破坏 T 细胞急性淋巴细胞白血病与脑膜细胞的黏附,从而减弱化疗耐药性。

CD99 antibody disrupts T-cell acute lymphoblastic leukemia adhesion to meningeal cells and attenuates chemoresistance.

机构信息

Division of Pediatric Hematology and Oncology, Department of Pediatrics, University of Minnesota, 420 Delaware St SE, MMC 366, Minneapolis, MN, 55455, USA.

Masonic Cancer Center, University of Minnesota, Minneapolis, MN, USA.

出版信息

Sci Rep. 2021 Dec 21;11(1):24374. doi: 10.1038/s41598-021-03929-x.

Abstract

Central nervous system (CNS) relapse is a significant cause of treatment failure among patients with acute lymphoblastic leukemia. In prior work we found that the meninges, the thin layer of tissue that covers the brain and spinal cord, harbor leukemia cells in the CNS. Importantly, direct interactions between leukemia and meningeal cells enabled leukemia chemoresistance. Herein, we show that an antibody targeting CD99, a transmembrane protein expressed on meningeal cells and many leukemia cells, disrupts adhesion between leukemia and meningeal cells and restores sensitivity of the leukemia cells to chemotherapy. This work identifies a mechanism regulating critical intercellular interactions within the CNS leukemia niche and may lead to novel therapeutic approaches for overcoming niche-mediated chemoresistance.

摘要

中枢神经系统 (CNS) 复发是急性淋巴细胞白血病患者治疗失败的一个重要原因。在之前的研究中,我们发现脑膜,即覆盖大脑和脊髓的薄层组织,是 CNS 中白血病细胞的藏身之处。重要的是,白血病细胞与脑膜细胞之间的直接相互作用使白血病具有化疗耐药性。在此,我们表明靶向跨膜蛋白 CD99 的抗体可破坏白血病细胞与脑膜细胞之间的黏附,并恢复白血病细胞对化疗的敏感性。这项工作确定了一种调节 CNS 白血病龛内关键细胞间相互作用的机制,可能为克服龛介导的化疗耐药性提供新的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f39/8692434/96145c3f4649/41598_2021_3929_Fig1_HTML.jpg

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