Ewan V A, Cieplinski W, Hancock W W, Goldschneider I, Boyd A W, Rickles F R
J Immunol. 1986 Apr 1;136(7):2408-15.
We describe the generation and characterization of a new monoclonal antibody, A1-3, which possesses two unique properties. First, A1-3 binds selectively to stimulated human monocytes. Secondly, A1-3 inhibits the procoagulant activity expressed by stimulated monocytes and by human brain tissue factor. Unstimulated human peripheral blood cells (granulocytes, lymphocytes, monocytes, red blood cells, and platelets), prepared in the absence of detectable endotoxin, express no procoagulant activity and fail to bind A1-3. Stimulation of peripheral blood monocytes. alveolar macrophages, or the monocyte-like cell line U937, however, results in the expression of procoagulant activity and the binding of A1-3. The surface antigen recognized by A1-3 was recovered from endotoxin-stimulated human monocyte vesicles by immune precipitation and demonstrated an apparent m.w. of approximately 52,000. It is proposed that the monoclonal antibody A1-3 detects a differentiation antigen on human monocytes that is expressed in response to stimuli for monocyte activation.
我们描述了一种新的单克隆抗体A1-3的产生和特性,它具有两个独特的性质。第一,A1-3选择性地结合受刺激的人单核细胞。第二,A1-3抑制受刺激的单核细胞和人脑组织因子所表达的促凝血活性。在不存在可检测内毒素的情况下制备的未受刺激的人外周血细胞(粒细胞、淋巴细胞、单核细胞、红细胞和血小板)不表达促凝血活性,也不与A1-3结合。然而,刺激外周血单核细胞、肺泡巨噬细胞或单核细胞样细胞系U937,会导致促凝血活性的表达和A1-3的结合。通过免疫沉淀从内毒素刺激的人单核细胞囊泡中回收了被A1-3识别的表面抗原,其表观分子量约为52,000。有人提出,单克隆抗体A1-3检测到人单核细胞上的一种分化抗原,该抗原在单核细胞激活刺激下表达。