Mannoni P, Janowska-Wieczorek A, Turner A R, McGann L, Turc J M
Hum Immunol. 1982 Dec;5(4):309-23. doi: 10.1016/0198-8859(82)90022-2.
Monoclonal antibodies (MCA) were obtained by immunizing BALB/c mice with 99% pure granulocytes from normal donors or with a whole leukocyte suspension obtained from a chronic myelogenous leukemia (CML) patient, and then fusing the mouse spleen cells with a 315-43 myeloma cell clone. Four MCA were selected and studied using ELISA, immunofluorescence, cytotoxicity assays, and FACS analysis. Antibodies 80H.1, 80H.3, and 80H.5 (from normals) and 81H.1 (from CML) detected antigens expressed on neutrophils. Antibodies 80H.1 and 80H.3 (IgG) also reacted with monocytes but not with other blood cell subsets. Antibodies 80H.5 and 81H.1 (IgM) were cytotoxic and reacted strongly with most of the cells of the neutrophil maturation sequence, i.e., myeloblasts, promyelocytes, myelocytes, and mature granulocytes. Antibodies 80H.5 and 81H.1 also inhibited CFU-GM growth stimulated by leukocyte feeder layers or placental conditioned media, but did not inhibit BFU-E and CFU-E. Antigens recognized by 80H.3, 80H.5, and 81H.1 were expressed both on a proportion of cells from HL.60, KG.1, ML.1, and K562 myeloid cell lines, and on a proportion of blast cells isolated from patients with acute myelogenous leukemia. They were not found on lymphoid cell lines or lymphoid leukemia cells. These MCA recognize either late differentiation antigens expressed on mature neutrophils and monocytes (80H.1 and 80H.3) or early differentiation antigens (80H.5 and 81H.1) specific to the granulocytic lineage. They may be useful for a better definition of those antigens specific to hematopoietic stem cells and their relationship with normal or neoplastic hematopoiesis.
通过用来自正常供体的99%纯粒细胞或来自一名慢性粒细胞白血病(CML)患者的全白细胞悬液免疫BALB/c小鼠,然后将小鼠脾细胞与315 - 43骨髓瘤细胞克隆融合,获得了单克隆抗体(MCA)。选择了四种MCA,并使用酶联免疫吸附测定(ELISA)、免疫荧光、细胞毒性测定和荧光激活细胞分选(FACS)分析进行研究。抗体80H.1、80H.3和80H.5(来自正常样本)以及81H.1(来自CML)检测到中性粒细胞上表达的抗原。抗体80H.1和80H.3(IgG)也与单核细胞反应,但不与其他血细胞亚群反应。抗体80H.5和81H.1(IgM)具有细胞毒性,并且与中性粒细胞成熟序列的大多数细胞,即原始粒细胞、早幼粒细胞、中幼粒细胞和成熟粒细胞强烈反应。抗体80H.5和81H.1也抑制由白细胞饲养层或胎盘条件培养基刺激的CFU - GM生长,但不抑制BFU - E和CFU - E。80H.3、80H.5和81H.1识别的抗原在HL.60、KG.1、ML.1和K562髓系细胞系的一部分细胞以及从急性髓性白血病患者分离的一部分原始细胞上均有表达。在淋巴细胞系或淋巴细胞白血病细胞上未发现这些抗原。这些MCA识别成熟中性粒细胞和单核细胞上表达的晚期分化抗原(80H.1和80H.3)或粒细胞系特有的早期分化抗原(80H.5和81H.1)。它们可能有助于更好地定义造血干细胞特有的那些抗原及其与正常或肿瘤性造血的关系。