Maldonado Mike, Diaz Luis A, Prisayanh Phillip, Yang Jinsheng, Qaqish Bahjat F, Aoki Valeria, Hans-Filho Gunter, Rivitti Evandro A, Culton Donna A, Qian Ye
Department of Dermatology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599.
Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599.
Immunohorizons. 2017 Aug 1;1(6):71-80. doi: 10.4049/immunohorizons.1700029.
We have shown that although the IgG response in fogo selvagem (FS) is mainly restricted to desmoglein (Dsg) 1, other keratinocyte cadherins are also targeted by FS patients and healthy control subjects living in the endemic region of Limão Verde, Brazil (endemic controls). Evaluating nonpathogenic IgG1 and pathogenic IgG4 subclass responses to desmosomal proteins may reveal important differences between pathogenic and nonpathogenic responses, and how these differences relate to the pathogenic IgG4 response and resultant FS. In this study, we tested by ELISA >100 sera from each FS patient, endemic control, and nonendemic control for IgG1 and IgG4 autoantibodies to keratinocyte cadherins besides Dsg1. IgG1 and IgG4 subclass responses in endemic controls are highly correlated between Dsg1 and other keratinocyte cadherins. This correlation persists in the IgG1 response among FS patients, but diminishes in IgG4 response, suggesting that IgG1 binds highly conserved linear epitopes among cadherins, whereas IgG4 binds mainly specific conformational epitopes on Dsg1. A confirmatory test comparing serum samples of 11 individuals before and after their FS onset substantiated our findings that IgG1 recognizes primarily linear epitopes on Dsg1 both before and after disease onset, whereas IgG4 recognizes primarily linear epitopes before disease onset, but recognizes more conformational epitopes on Dsg1 after the onset of disease. This study may provide a mechanism by which a specificity convergence of the IgG4 response to unique Dsg1 epitopes, most likely conformational pathogenic epitopes, leads to the onset of FS disease.
我们已经表明,尽管灼口综合征(FS)中的IgG反应主要局限于桥粒芯糖蛋白(Dsg)1,但生活在巴西绿柠檬流行地区的FS患者和健康对照者(地方病对照)也会针对其他角质形成细胞钙黏蛋白产生反应。评估对桥粒蛋白的非致病性IgG1和致病性IgG4亚类反应,可能会揭示致病性和非致病性反应之间的重要差异,以及这些差异与致病性IgG4反应和由此导致的FS之间的关系。在本研究中,我们通过酶联免疫吸附测定(ELISA)检测了来自每位FS患者、地方病对照和非地方病对照的100多份血清,以检测除Dsg1外针对角质形成细胞钙黏蛋白的IgG1和IgG4自身抗体。在地方病对照中,Dsg1与其他角质形成细胞钙黏蛋白之间的IgG1和IgG4亚类反应高度相关。这种相关性在FS患者的IgG1反应中持续存在,但在IgG4反应中减弱,这表明IgG1结合钙黏蛋白中高度保守的线性表位,而IgG4主要结合Dsg1上的特定构象表位。一项比较11名个体FS发病前后血清样本的验证性试验证实了我们的发现,即IgG1在疾病发作前后主要识别Dsg1上的线性表位,而IgG4在疾病发作前主要识别线性表位,但在疾病发作后识别Dsg1上更多的构象表位。本研究可能提供了一种机制,通过这种机制,IgG4对独特的Dsg1表位(最有可能是构象致病性表位)的特异性趋同导致了FS疾病的发作。