Laboratory of the Dermatology Division, Hospital das Clínicas, Faculty of Medicine of Ribeirão Preto, Universidade de São Paulo, São Paulo, SP, Brazil.
Division of Dermatology, Department of Internal Medicine, Faculty of Medicine of Ribeirão Preto, Universidade de São Paulo, São Paulo, SP, Brazil.
An Bras Dermatol. 2024 Sep-Oct;99(5):680-687. doi: 10.1016/j.abd.2023.11.006. Epub 2024 Jun 8.
Anti-desmoglein (Dsg)1 is produced in pemphigus foliaceus (PF), affecting exclusively the skin. Pemphigus vulgaris (PV) shows the production of anti-Dsg3 in the mucosal form, and anti-Dsg1 and 3 in the mucocutaneous form. Anti-Dsg3 autoantibodies have been rarely reported in PF.
To determine the factors associated with the production and pathogenicity of anti-Dsg3 in PF.
Comparative analytical study of three patients groups: 16 PF-anti-Dsg3+, and 42 PF-anti-Dsg3(-) and 22 PV treatment-naïve cases. Serum was used in the anti-Dsg1 and 3 ELISA, and in immunoblotting (IB) with human epidermis extract. The expression of Dsg1 and 3 in paraffin sections was analyzed by immunohistochemistry (IHC). HLA-DRB1 alleles were compiled from a database.
In the PF-anti-Dsg3+ group: age range similar to that of the PV group (p > 0.9999); predominance of the generalized form of PF (p = 0.002); anti-Dsg3 titers lower than those of PV (p < 0.0001); IB confirmed Dsg3 identification in one (8.33%) of 12 patients; IHC showed exclusive cytoplasmic internalization of Dsg1; HLA-DRB1 alleles of susceptibility to PF, with the absence of alleles associated with PV, in the five typed patients.
Most of the patients in the PF-anti-Dsg3+ group were undergoing treatment.
The presence of anti-Dsg3 antibodies in PF was related to older age (comparable to that of PV) and the generalized form of PF. The non-pathogenicity of anti-Dsg3 antibodies in PF can be attributed to the low serum anti-Dsg3 titers, the lack of Dsg3 internalization as detected by IHC, and the absence of PV-associated HLA-DRB1 alleles.
抗桥粒芯糖蛋白 1(Dsg)1 存在于落叶型天疱疮(PF)中,仅影响皮肤。寻常型天疱疮(PV)在黏膜型中产生抗 Dsg3,在黏膜皮肤型中产生抗 Dsg1 和 3。抗 Dsg3 自身抗体在 PF 中很少有报道。
确定与 PF 中抗 Dsg3 的产生和致病性相关的因素。
对三组患者进行比较分析:16 例 PF-抗 Dsg3+,42 例 PF-抗 Dsg3-和 22 例未经治疗的 PV 患者。采用 ELISA 检测血清中的抗 Dsg1 和 3,采用免疫印迹(IB)检测人表皮提取物。采用免疫组化(IHC)检测石蜡切片中 Dsg1 和 3 的表达。从数据库中编译 HLA-DRB1 等位基因。
在 PF-抗 Dsg3+组中:年龄范围与 PV 组相似(p>0.9999);PF 全身性形式占优势(p=0.002);抗 Dsg3 滴度低于 PV(p<0.0001);IB 证实 12 例患者中有 1 例(8.33%)存在 Dsg3 鉴定;IHC 显示 Dsg1 仅存在细胞质内内化;在 5 例定型患者中,PF 易感 HLA-DRB1 等位基因缺失与 PV 相关的等位基因。
PF-抗 Dsg3+组中的大多数患者正在接受治疗。
PF 中存在抗 Dsg3 抗体与年龄较大(与 PV 相当)和 PF 的全身性形式有关。PF 中抗 Dsg3 抗体的非致病性可归因于血清抗 Dsg3 滴度较低、IHC 检测到的 Dsg3 内化缺乏以及与 PV 相关的 HLA-DRB1 等位基因缺失。