Tuson J R, Pascoe E W, Jacob D A
Department of Surgery, University of Cambridge, United Kingdom.
J Histochem Cytochem. 1990 Jul;38(7):923-6. doi: 10.1177/38.7.2355173.
We describe a novel immunohistochemical technique which permits the detection of specific binding of human monoclonal antibodies (MAb) to cryostat sections of human tissues. The technique overcomes the problem of background staining caused by the presence of endogenous immunoglobulins in tissue sections. This is achieved by the formation of a molecular complex of the primary antibody (a human MAb), horseradish peroxidase-conjugated goat anti-human immunoglobulin, and normal human serum. This complex is then incubated with cryostat sections of human tissue, and binding of the complex is demonstrated using diaminobenzidine/hydrogen peroxide. The method is suitable for immunohistochemical screening of small samples of tissue culture supernatant for the presence of human MAb of potential interest, and for determining the pattern of binding of such MAb to a wide range of normal and pathological human tissues.
我们描述了一种新型免疫组织化学技术,该技术可检测人单克隆抗体(MAb)与人体组织冰冻切片的特异性结合。该技术克服了组织切片中内源性免疫球蛋白导致背景染色的问题。这是通过一级抗体(人单克隆抗体)、辣根过氧化物酶偶联的山羊抗人免疫球蛋白和正常人血清形成分子复合物来实现的。然后将该复合物与人体组织的冰冻切片一起孵育,并使用二氨基联苯胺/过氧化氢来显示复合物的结合情况。该方法适用于对组织培养上清液的小样本进行免疫组织化学筛选,以检测潜在感兴趣的人单克隆抗体的存在,并确定此类单克隆抗体与多种正常和病理人体组织的结合模式。