Lazzaro B, Strassburg A
Department of Pathology and Laboratory Medicine, Temple University Hospital, Philadelphia, Pennsylvania 19140, USA.
Hybridoma. 1996 Apr;15(2):141-6. doi: 10.1089/hyb.1996.15.141.
Studies of antigen expression in dysplastic nevi have been limited to some extent by difficulties in obtaining frozen nevi with which to react monoclonal antibodies. Accordingly, we obtained a panel of antibodies that binds to antigens preserved in paraffin-embedded tissue. This panel of monoclonal antibodies, raised against nevomelanoma antigens, was used on 26 dysplastic compound nevi and additionally on 14 invasive superficial spreading melanomas. Among the dysplastic nevi, two basic dermal staining patterns emerged. One pattern designated "Type 1" shows a histologically well-developed dermal component that tends to be antigenically well stratified, with the cells in the upper dermis expressing the most antigen, and gradual loss of antigenicity in the lower dermis as maturation of nevic cells occurs. A second ("Type 2") pattern was seen in which nevic cells tended to remain in the upper dermis, with less downgrowth, and to express antigen in a diffuse or patchy, but nonstratified distribution. Some differential distribution of the antigens was noted, with antibodies 404-101, HMB-45, and ME 109 binding to the activated junctional zone, but showing lower binding affinity within the dermis. ME 491, NKI-C3, and 506 bind to antigens abundant in the junctional zone as well as the dermis. The antibody ME 67-6 binds to both junction and dermis, but is more useful for delineation of antigenic stratification and presence of abnormal "clones."
发育异常痣中抗原表达的研究在一定程度上受到获取用于与单克隆抗体反应的冷冻痣的困难的限制。因此,我们获得了一组与石蜡包埋组织中保存的抗原结合的抗体。这组针对痣黑色素瘤抗原产生的单克隆抗体被用于26个发育异常复合痣,另外还用于14个侵袭性浅表扩散性黑色素瘤。在发育异常痣中,出现了两种基本的真皮染色模式。一种模式称为“1型”,显示组织学上发育良好的真皮成分,其抗原分层良好,真皮上层的细胞表达最多的抗原,随着痣细胞成熟,真皮下层的抗原性逐渐丧失。第二种(“2型”)模式表现为痣细胞倾向于留在真皮上层,向下生长较少,并以弥漫性或斑片状但不分层的分布表达抗原。注意到抗原存在一些差异分布,抗体404 - 101、HMB - 45和ME 109与活化的交界区结合,但在真皮内显示较低的结合亲和力。ME 491、NKI - C3和506与交界区以及真皮中丰富的抗原结合。抗体ME 67 - 6与交界区和真皮都结合,但更有助于描绘抗原分层和异常“克隆”的存在。