Letesson J J, Coppe P, Lostrie-Trussart N, Depelchin A
Anim Blood Groups Biochem Genet. 1983;14(4):239-50.
A monoclonal antibody termed B2 Val 7C7, was produced by the fusion of xenoimmune mouse spleen cells with Sp2/0.Ag 14 myeloma cells. This antibody is specific for a polymorphic lymphocyte antigen; it was detected on cells from 138 out of 177 cattle by both 125I-labelled protein A (solid-phase radioimmunoassay, SPRIA) and gold-labelled protein A (immunogold). Its binding was tested on various cell types (peripheral blood lymphocytes, monocytes, polymorphonuclear cells (PMN), thymocytes) from a variety of normal bovine donors. On the one hand, B2 Val 7C7 detects a determinant present on all IgG-bearing lymphocytes, on 20% of the non-IgG-bearing lymphocytes and on the majority of the monocytes. On the other hand, no binding occurs on any PMN or thymocytes. The detected membrane antigen was isolated by immunoprecipitation from an NP 40 extract of 3H-leucine-labelled cells. On SDS-PAGE, it appears to be composed of two sub-units: a 32 000-dalton and a 27 000-dalton chain. These results show that B2 Val 7C7 recognizes an alloantigenic specificity present on an Ia-like antigen.
一种名为B2 Val 7C7的单克隆抗体是通过将异种免疫小鼠脾细胞与Sp2/0.Ag 14骨髓瘤细胞融合产生的。该抗体对一种多态性淋巴细胞抗原具有特异性;通过125I标记的蛋白A(固相放射免疫测定,SPRIA)和金标记的蛋白A(免疫金)在177头牛中的138头牛的细胞上检测到了这种抗原。在来自各种正常牛供体的多种细胞类型(外周血淋巴细胞、单核细胞、多形核细胞(PMN)、胸腺细胞)上测试了其结合情况。一方面,B2 Val 7C7检测到所有携带IgG的淋巴细胞、20%不携带IgG的淋巴细胞以及大多数单核细胞上存在的一种决定簇。另一方面,在任何PMN或胸腺细胞上均未发生结合。通过免疫沉淀从3H-亮氨酸标记细胞的NP 40提取物中分离出检测到的膜抗原。在SDS-PAGE上,它似乎由两个亚基组成:一条32000道尔顿的链和一条27000道尔顿的链。这些结果表明,B2 Val 7C7识别存在于一种Ia样抗原上的同种抗原特异性。