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三种单克隆抗体可识别所有马T淋巴细胞上的抗原,以及两个相互排斥的T淋巴细胞亚群。

Three monoclonal antibodies identifying antigens on all equine T lymphocytes, and two mutually exclusive T-lymphocyte subsets.

作者信息

Lunn D P, Holmes M A, Duffus W P

机构信息

Department of Clinical Veterinary Medicine, University of Cambridge, U.K.

出版信息

Immunology. 1991 Oct;74(2):251-7.

Abstract

The aim of this study was to produce monoclonal antibodies (mAb) recognizing equine lymphocyte surface antigens. Fusions were conducted using BALB/c mice hyperimmunized with equine thymocytes. Hybridoma supernatants were screened by flow cytometry and positive hybridomas were cloned twice by limiting dilution. These mAb were then characterized for tissue distribution by immunohistology and flow cytometry, and by precipitation and analysis of the lymphocyte antigens which they recognized. Three mAb (CVS5, CVS4 and CVS8) are described which recognize only T lymphocytes in peripheral blood. Two-colour immunofluorescent studies showed that CVS5 recognized all T lymphocytes and that CVS4 and CVS8 recognized two mutually exclusive subsets of CVS5-positive cells. In the thymus there was a large population of CVS4/CVS8 double-positive cells. Immunohistochemical staining with these mAb was restricted to T-lymphocyte areas. CVS4 and CVS5 precipitated molecules of 58,000 and 69,000 MW, respectively, in both reducing and non-reducing conditions. CVS8 precipitated two molecules of 32,000 and 39,000 MW in reducing conditions, and one molecule of 69,000 MW in non-reducing conditions. This evidence suggests that CVS5, CVS4 and CVS8 recognize the equine homologues of CD5, CD4 and CD8, and that the characteristics of these antigens are similar to those of other species.

摘要

本研究的目的是制备识别马淋巴细胞表面抗原的单克隆抗体(mAb)。使用经马胸腺细胞超免疫的BALB/c小鼠进行细胞融合。通过流式细胞术筛选杂交瘤上清液,并通过有限稀释法对阳性杂交瘤进行两次克隆。然后通过免疫组织学和流式细胞术对这些单克隆抗体的组织分布进行表征,并对它们识别的淋巴细胞抗原进行沉淀和分析。描述了三种单克隆抗体(CVS5、CVS4和CVS8),它们仅识别外周血中的T淋巴细胞。双色免疫荧光研究表明,CVS5识别所有T淋巴细胞,而CVS4和CVS8识别CVS5阳性细胞的两个相互排斥的亚群。在胸腺中存在大量CVS4/CVS8双阳性细胞。用这些单克隆抗体进行的免疫组织化学染色仅限于T淋巴细胞区域。在还原和非还原条件下,CVS4和CVS5分别沉淀出分子量为58,000和69,000的分子。在还原条件下,CVS8沉淀出分子量为32,000和39,000的两个分子,在非还原条件下沉淀出一个分子量为69,000的分子。这一证据表明,CVS5、CVS4和CVS8识别CD5、CD4和CD8的马同源物,并且这些抗原的特征与其他物种的相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3a6/1384601/aed41e8170e3/immunology00113-0082-a.jpg

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