J J Letesson, P Coppe, N Lostrie-Trussart, A Depelchin
{"title":"A bovine 'Ia-like' antigen detected by a xenogeneic monoclonal antibody.","authors":"J J Letesson, P Coppe, N Lostrie-Trussart, A Depelchin","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":7809,"journal":{"name":"Animal blood groups and biochemical genetics","volume":"14 4","pages":"239-50"},"PeriodicalIF":0.0000,"publicationDate":"1983-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Animal blood groups and biochemical genetics","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
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.
用Sp2/0与异种免疫小鼠脾细胞融合制备单克隆抗体B2 Val 7C7。ag14骨髓瘤细胞。这种抗体对多态淋巴细胞抗原具有特异性;用125i标记蛋白A(固相放射免疫测定法,SPRIA)和金标记蛋白A(免疫金)对177头牛中的138头细胞进行检测。它的结合测试了各种细胞类型(外周血淋巴细胞、单核细胞、多形核细胞(PMN)、胸腺细胞)从各种正常的牛供体。一方面,B2 Val 7C7检测到存在于所有携带igg的淋巴细胞、20%的非携带igg的淋巴细胞和大多数单核细胞上的决定因子。另一方面,没有结合发生在任何PMN或胸腺细胞上。通过免疫沉淀从3h -亮氨酸标记细胞的NP 40提取物中分离检测到的膜抗原。在SDS-PAGE上,它似乎由两个亚单元组成:一个32000道尔顿和一个27000道尔顿链。这些结果表明B2 Val 7C7识别ia样抗原上存在的同种抗原特异性。