Janowska-Wieczorek A, Mannoni P, Turner A R, McGann L E, Shaw A R, Turc J M
Br J Haematol. 1984 Sep;58(1):159-68. doi: 10.1111/j.1365-2141.1984.tb06070.x.
A murine monoclonal antibody (82H5, IgM class) has been developed that detects an antigenic determinant expressed by greater than 90% of normal granulocytes and 60-80% of light-density normal bone-marrow cells, including human pluripotential progenitors (colony-forming-unit-granulocyte, erythroid, macrophage, megakaryocyte; CFU-GEMM) and committed progenitors: granulocyte-macrophage (CFU-GM), erythroid (BFU-E), and megakaryocytic (CFU-MK). This antibody did not react with erythrocytes, monocytes, platelets, lymphocytes from normal peripheral blood, lymphoblasts from patients with acute lymphoblastic leukaemia, or with lymphoid cells lines. The 82H5-defined antigenic determinant was expressed on greater than 90% of leukaemic cells of promyelocytic, myelomonocytic and monocytic morphology, and cell lines KG.1, ML.1, HL.60, K562 and U.937. Cortical thymocytes were unreactive with 82H5. Treatment of human bone-marrow cells with granulocytic-specific monoclonal antibody 82H5 plus complement significantly inhibited colony formation (48-74%; P less than 0.05) of CFU-GEMM, CFU-GM, BFU-E, CFU-MK, whereas treatment with control monoclonal anti-Ia antibody plus complement caused 79-89% inhibition. This antibody reacted strongly with 3-fuc-NAc lactosamine when tested with a panel of synthetic carbohydrate structures. We conclude that 82H5 may be a useful probe for phenotypic analysis of leukaemic cells and investigation of haematopoiesis.
已研制出一种鼠单克隆抗体(82H5,IgM类),它能检测到一种抗原决定簇,该抗原决定簇在超过90%的正常粒细胞以及60 - 80%的低密度正常骨髓细胞中表达,包括人类多能祖细胞(集落形成单位 - 粒细胞、红细胞、巨噬细胞、巨核细胞;CFU - GEMM)和定向祖细胞:粒细胞 - 巨噬细胞(CFU - GM)、红细胞(BFU - E)和巨核细胞(CFU - MK)。该抗体不与红细胞、单核细胞、血小板、正常外周血淋巴细胞、急性淋巴细胞白血病患者的淋巴母细胞或淋巴细胞系发生反应。82H5所定义的抗原决定簇在早幼粒细胞、粒单核细胞和单核细胞形态的白血病细胞以及细胞系KG.1、ML.1、HL.60、K562和U.937中,超过90%的细胞上表达。皮质胸腺细胞与82H5无反应。用粒细胞特异性单克隆抗体82H5加补体处理人骨髓细胞,可显著抑制CFU - GEMM、CFU - GM、BFU - E、CFU - MK的集落形成(48 - 74%;P小于0.05),而用对照单克隆抗Ia抗体加补体处理则导致79 - 89%的抑制。当用一组合成碳水化合物结构进行检测时,该抗体与3 - fuc - NAc乳糖胺强烈反应。我们得出结论,82H5可能是白血病细胞表型分析和造血研究的有用探针。