Mason D Y, Krissansen G W, Davey F R, Crumpton M J, Gatter K C
Nuffield Department of Pathology, John Radcliffe Hospital, Oxford.
J Clin Pathol. 1988 Feb;41(2):121-7. doi: 10.1136/jcp.41.2.121.
Polyclonal rat antisera, raised against affinity purified CD3 antigen, gave strong immunoenzymatic labelling of T cells in routine paraffin embedded sections, with negligible background staining. The specificity of these reactions was confirmed by staining biopsy specimens from 21 previously phenotyped non-Hodgkin's lymphomas (including 14 of T cell origin and six of B cell origin). It is suggested that the ability of the polyclonal anti-CD3 antisera to detect T cells in paraffin sections is due to the presence in these sera of antibodies against fixation resistant epitopes on CD3 antigen, and that immunisation with purified denatured preparations of other white cell associated antigens may broaden the range of antibodies suitable for the phenotypic analysis of leucocytes in routine histological samples.
用针对亲和纯化的CD3抗原产生的多克隆大鼠抗血清,对常规石蜡包埋切片中的T细胞进行了强烈的免疫酶标记,背景染色可忽略不计。通过对21例先前已进行表型分析的非霍奇金淋巴瘤(包括14例T细胞起源和6例B细胞起源)的活检标本进行染色,证实了这些反应的特异性。有人提出,多克隆抗CD3抗血清在石蜡切片中检测T细胞的能力,是由于这些血清中存在针对CD3抗原上抗固定表位的抗体,并且用其他白细胞相关抗原的纯化变性制剂进行免疫,可能会扩大适用于常规组织学样本中白细胞表型分析的抗体范围。