Ashman L K, Aylett G W, Mehrabani P A, Bendall L J, Niutta S, Cambareri A C, Cole S R, Berndt M C
Department of Microbiology and Immunology, University of Adelaide, South Australia.
Br J Haematol. 1991 Oct;79(2):263-70. doi: 10.1111/j.1365-2141.1991.tb04531.x.
A murine monoclonal antibody 14A2.H1, raised against acute myeloid leukaemia cells, identifies a previously undescribed 27 kDa platelet surface glycoprotein which is expressed at low copy number (10(3)/platelet). MAb 14A2.H1 caused aggregation of platelets which was dependent on Fc gamma RII. Binding of the antibody to platelets was not altered by activation by thrombin or phorbol ester. In haemopoietic cell populations the antibody bound to megakaryocytes, monocytes (weakly), several myeloid leukaemic cell lines and fresh myeloid leukaemic blasts from some patients. Lymphocytes, lymphoid cell lines, neutrophils and haemopoietic progenitor cells were negative. Expression of the antigen was not restricted to haemopoietic cells as epithelial cells in tonsillar crypts and endothelial cells were positive.
一种针对急性髓系白血病细胞产生的鼠单克隆抗体14A2.H1,识别出一种先前未描述的27 kDa血小板表面糖蛋白,该蛋白以低拷贝数(10³/血小板)表达。单克隆抗体14A2.H1引起血小板聚集,这依赖于FcγRII。抗体与血小板的结合不受凝血酶或佛波酯激活的影响。在造血细胞群体中,该抗体与巨核细胞、单核细胞(弱阳性)、几种髓系白血病细胞系以及一些患者的新鲜髓系白血病原始细胞结合。淋巴细胞、淋巴样细胞系、中性粒细胞和造血祖细胞呈阴性。该抗原的表达并不局限于造血细胞,因为扁桃体隐窝中的上皮细胞和内皮细胞呈阳性。