Tadini G, Kanitakis J, Cavalli R, Schmitt D, Cambiaghi S, Berti E
Center for Inherited Cutaneous Diseases, IRCCS Ospedale Maggiore, University of Milan, Italy.
Arch Dermatol Res. 1995;287(8):699-704. doi: 10.1007/BF01105792.
NU-T2 antigen (Ag) is a new and recently described antigen of the dermal-epidermal junction, recognized by an anti-CD1b monoclonal antibody denominated NU-T2. We studied NU-T2 Ag expression in junctional epidermolysis bullosa (13 patients) and in other forms of hereditary epidermolysis bullosa (23 patients), comparing the results with nicein expression. In junctional epidermolysis bullosa gravis type no differences were found between the expression of NU-T2 and nicein, both being negative in bullous as well as in non-bullous skin. Interestingly, in mitis type junctional epidermolysis bullosa, NU-T2 Ag was found to be absent or reduced in five of six patients both in lesional and in uncleaved skin. When compared with nicein expression, clearcut differences were found, further suggesting that these two antigens are different. These data confirm that NU-T2 Ag is a novel epitope of the dermal-epidermal junction, probably relevant in dermal-epidermal cohesion, and it could be responsible, together with nicein, 19-DEJ-1 and other adhesion molecules, for the different subtypes of junctional epidermolysis bullosa. Finally, NU-T2 monoclonal antibody is a new relevant tool for the diagnosis, classification, and prenatal diagnosis of junctional epidermolysis bullosa.
NU-T2抗原(Ag)是一种新的、最近才被描述的真皮-表皮交界处抗原,可被一种名为NU-T2的抗CD1b单克隆抗体识别。我们研究了交界型大疱性表皮松解症(13例患者)和其他形式的遗传性大疱性表皮松解症(23例患者)中NU-T2 Ag的表达情况,并将结果与奈辛表达进行比较。在重型交界型大疱性表皮松解症中,未发现NU-T2和奈辛的表达有差异,在水疱性和非水疱性皮肤中二者均为阴性。有趣的是,在轻型交界型大疱性表皮松解症中,6例患者中有5例在皮损处和未裂开皮肤中均未检测到或检测到减少的NU-T2 Ag。与奈辛表达相比,发现了明显差异,进一步表明这两种抗原不同。这些数据证实,NU-T2 Ag是真皮-表皮交界处的一种新表位,可能与真皮-表皮黏附有关,并且它可能与奈辛、19-DEJ-1和其他黏附分子一起,导致了交界型大疱性表皮松解症的不同亚型。最后,NU-T2单克隆抗体是交界型大疱性表皮松解症诊断、分类和产前诊断的一种新的重要工具。