Uchiyama T, Ishikawa T, Imura A
Research Center for Immunodeficiency Virus, Kyoto University, Japan.
J Acquir Immune Defic Syndr Hum Retrovirol. 1996;13 Suppl 1:S114-8. doi: 10.1097/00042560-199600001-00019.
Cell adhesion molecules expressed on the cell surface of leukemic cells and on vascular endothelial cells may play a key role in trafficking, localization, and infiltration of leukemic cells in adult T-cell leukemia (ATL). The predominant adhesion pathway between ATL cells or human T-cell leukemia virus type I (HTLV-I)-infected cell lines and human umbilical vein endothelial cells (HUVECs) is an E-selectin-mediated pathway as determined by studies using adhesion-blocking monoclonal antibodies, although fresh leukemic cells and HTLV-I-infected cell lines also expressed LFA-I, VLA-4, L-selectin, and CD44. Our study also strongly suggested the presence of adhesion pathway(s) mediated by as yet unknown cell adhesion molecule(s), to which we have recently developed monoclonal antibodies.
白血病细胞和血管内皮细胞表面表达的细胞黏附分子可能在成人T细胞白血病(ATL)中白血病细胞的迁移、定位和浸润过程中起关键作用。尽管新鲜白血病细胞和人T细胞白血病病毒I型(HTLV-I)感染的细胞系也表达淋巴细胞功能相关抗原-1(LFA-1)、极迟抗原-4(VLA-4)、L-选择素和CD44,但通过使用黏附阻断单克隆抗体的研究确定,ATL细胞或HTLV-I感染的细胞系与人脐静脉内皮细胞(HUVECs)之间的主要黏附途径是E-选择素介导的途径。我们的研究还强烈提示存在由尚未知晓的细胞黏附分子介导的黏附途径,我们最近已针对这些分子研制出单克隆抗体。