Mason D Y, Cordell J, Brown M, Pallesen G, Ralfkiaer E, Rothbard J, Crumpton M, Gatter K C
Department of Pathology, John Radcliffe Hospital, Headington, Oxford.
J Clin Pathol. 1989 Nov;42(11):1194-200. doi: 10.1136/jcp.42.11.1194.
Rabbit polyclonal antibodies were raised against a proline rich, peptide sequence, comprising 13 amino acids, in the cytoplasmic domain of the CD3 epsilon chain. Immunoprecipitation experiments showed that this antibody preparation recognised the CD3 antigen on human T lymphoblasts. The antibody stained normal T cells strongly in tissue sections which had been fixed in formalin or Bouin's solution and embedded in paraffin wax. Its reactivity with T cell lymphoma, when evaluated on a series of 96 previously phenotyped cases, closely agreed with the results obtained on cryostat sections. These results indicate that the specific detection of T cells in routinely processed tissue biopsy specimens is now technically feasible on a wide scale in diagnostic laboratories using CD3 peptide antibodies, and they also suggest that in future the use of anti-peptide antibodies may detect other lineage specific antigenic markers in paraffin wax sections.
针对CD3ε链胞质结构域中富含脯氨酸的13个氨基酸的肽序列制备了兔多克隆抗体。免疫沉淀实验表明,该抗体制剂可识别人类T淋巴母细胞上的CD3抗原。该抗体在经福尔马林或布安氏溶液固定并石蜡包埋的组织切片中能强烈染色正常T细胞。在对96例先前已进行表型分析的病例进行评估时,其与T细胞淋巴瘤的反应性与冰冻切片的结果高度一致。这些结果表明,在诊断实验室中,使用CD3肽抗体在常规处理的组织活检标本中特异性检测T细胞在技术上现已广泛可行,并且还表明,未来使用抗肽抗体可能会在石蜡切片中检测到其他谱系特异性抗原标记物。