Takaishi M, Fu S M
J Immunol. 1985 Aug;135(2):1523-9.
A series of monoclonal antibodies (mAb) were raised against nonlymphoid leukemic cell lines. Three of them have been characterized in detail. mAb H8 (IgG2), mAB U2 (IgG1), and mAb ML143 (IgM) were established with HEL, an erythroleukemia cell line, U937, a monocytoid (histiocytic) line, and ML-1, a myeloid cell line as immunogen, respectively. A 65 to 75 KD polypeptide was precipitated from monocytes by mAb H8, a 160 KD protein from monocytes by mAb U2, and two broad bands in the regions of 150 and 195 KD from granulocytes by mAb ML143. All three mAb stained peripheral blood monocytes and granulocytes, but not lymphocytes, platelets, and erythrocytes. The mAb reacted with immature myeloid cells in bone marrow, ranging from myeloblasts to mature myelomonocytic cells. They also were reactive with various nonlymphoid cell lines and leukemia of myelomonocytic origin. They did not react with B cell lines and B cell CLL cells. By complement-mediated cytolysis and/or an immune rosette method, antigens H8 and U2 were found to be expressed on the vast majority of CFU-GM (14 days) progenitors but not on BFU-E. Antigen ML143 was not expressed by either progenitor. Furthermore, ML143 antigen was found on T leukemia cell lines, a subpopulation of mitogen-activated T cells, and certain non-T/non-B ALL cells. This reactivity was not found with mAb H8 and U2. The relationship between these mAb and those reported are discussed. The possibility of using these mAb to obtain a markedly enriched CFU-GM progenitor population is also raised.
制备了一系列针对非淋巴细胞白血病细胞系的单克隆抗体(mAb)。其中三种已得到详细鉴定。mAb H8(IgG2)、mAb U2(IgG1)和mAb ML143(IgM)分别以红白血病细胞系HEL、单核细胞样(组织细胞样)细胞系U937和髓样细胞系ML-1作为免疫原而建立。mAb H8从单核细胞中沉淀出一条65至75KD的多肽,mAb U2从单核细胞中沉淀出一种160KD的蛋白质,mAb ML143从粒细胞中沉淀出150和195KD区域的两条宽带。所有这三种mAb均能染色外周血单核细胞和粒细胞,但不能染色淋巴细胞、血小板和红细胞。这些mAb与骨髓中的未成熟髓样细胞反应,范围从成髓细胞到成熟的髓单核细胞。它们也与各种非淋巴细胞系和髓单核细胞起源的白血病反应。它们不与B细胞系和B细胞慢性淋巴细胞白血病细胞反应。通过补体介导的细胞溶解和/或免疫玫瑰花结法发现,抗原H8和U2在绝大多数CFU-GM(14天)祖细胞上表达,但在BFU-E上不表达。两种祖细胞均不表达抗原ML143。此外,在T白血病细胞系、有丝分裂原激活的T细胞亚群和某些非T/非B急性淋巴细胞白血病细胞上发现了ML143抗原。mAb H8和U2未发现这种反应性。讨论了这些mAb与已报道的mAb之间的关系。还提出了使用这些mAb获得明显富集的CFU-GM祖细胞群体的可能性。