Zambruno G, Gielen V, Schmitt D, Dezutter-Dambuyant C, Thivolet J
INSERM U 209, Laboratoire de Recherche Dermatologique et Immunologie, Hôpital Edouard Herriot, Lyon, France.
J Cutan Pathol. 1987 Dec;14(6):331-6. doi: 10.1111/j.1600-0560.1987.tb01533.x.
In this work the role of trypsin in revealing epidermal cell surface antigens, with the use of immunological markers, was investigated. Two monoclonal antibodies (MCA) were used, the first: D47, belongs to the first cluster of differentiation and recognizes a membrane antigen of human thymocytes; the second HLA-ABC-m3, is an anti-HLA-B27 MCA. Preliminary treatment with various concentrations of trypsin was performed on frozen skin sections and followed by indirect immunofluorescence. D47 reacted with epidermal dendritic cells only after trypsin pretreatment of skin sections. In addition a mild preliminary trypsinization was shown to increase in situ immunoreactivity of MCA HLA-ABC-m3 with epidermal cells. Best results were obtained when trypsin concentrations ranging from 2.5 to 5 micrograms/ml were applied for 10 min at 37 degrees C. Preliminary trypsinization may be of interest for a better exposure of some surface antigens to immunohistochemical markers.
在这项工作中,研究了胰蛋白酶在利用免疫标记物揭示表皮细胞表面抗原方面的作用。使用了两种单克隆抗体(MCA),第一种:D47,属于第一分化簇,识别人类胸腺细胞的一种膜抗原;第二种HLA-ABC-m3,是一种抗HLA-B27 MCA。对冷冻皮肤切片进行不同浓度胰蛋白酶的预处理,然后进行间接免疫荧光检测。仅在皮肤切片经胰蛋白酶预处理后,D47才与表皮树突状细胞发生反应。此外,轻度的胰蛋白酶预处理显示可增强MCA HLA-ABC-m3与表皮细胞的原位免疫反应性。当在37℃下应用2.5至5微克/毫升的胰蛋白酶浓度处理10分钟时,可获得最佳结果。初步的胰蛋白酶处理对于某些表面抗原更好地暴露于免疫组织化学标记物可能具有重要意义。