西格莱克
CD33
髓样
抗体
唾液酸
川地34
干细胞
单克隆抗体
髓系白血病
抗原
生物
免疫学
分化群
K562细胞
白血病
分子生物学
细胞
细胞生物学
生物化学
作者
Huan Cao,Andreas Neerincx,Bernard de Bono,Ursula Lakner,Catherine Huntington,John Elvin,Emma Gudgin,Clare Pridans,Mark A. Vickers,Brian J.P. Huntly,John Trowsdale,Alexander D. Barrow
摘要
Sialic acid-binding immunoglobulin-like lectin (Siglec)-15 has recently been identified as a critical tumour checkpoint, augmenting the expression and function of programmed death-ligand 1. We raised a monoclonal antibody, A9E8, specific for Siglec-15 using phage display. A9E8 stained myeloid leukaemia cell lines and peripheral cluster of differentiation (CD)33+ blasts and CD34+ leukaemia stem cells from patients with acute myeloid leukaemia (AML). By contrast, there was minimal expression on healthy donor leucocytes or CD34+ stem cells from non-AML donors, suggesting targeting Siglec-15 may have significant therapeutic advantages over its fellow Siglec CD33. After binding, A9E8 was rapidly internalised (half-life of 180 s) into K562 cells. Antibodies to Siglec-15 therefore hold therapeutic potential for AML treatment.
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