Khil'chenko Stanislav, Boch Katharina, van Beek Nina, Vorobyev Artem, Zillikens Detlef, Schmidt Enno, Ludwig Ralf J
Lübeck Institute of Experimental Dermatology, University of Lübeck, Lübeck, Germany.
Center for Research on Inflammation of the Skin, University of Lübeck, Lübeck, Germany.
Front Med (Lausanne). 2020 Sep 2;7:472. doi: 10.3389/fmed.2020.00472. eCollection 2020.
Pemphigus and pemphigoid diseases are organ-specific autoimmune diseases of the skin and/or mucous membranes, which are caused by autoantibodies targeting structural proteins of the skin. In other autoimmune diseases, a high prevalence of primary antibody deficiencies was noted. Conversely, a high prevalence of autoimmune diseases is reported in patients with primary antibody deficiencies. With the exception of one study, pointing toward a decrease of IgG in pemphigus patients, with a relative enrichment of IgG4, serum immunoglobulin (Ig) concentrations had not been studied in pemphigus and pemphigoid. Hence, we here aimed to investigate serum concentrations of IgM, IgA, IgG, and IgG1-4 in pemphigus and pemphigoid patients, as well as in healthy controls. Serum Ig concentrations were determined by ELISA in 105 healthy controls, 100 pemphigus vulgaris (PV), 100 pemphigus foliaceus, 99 bullous pemphigoid (BP), and 55 linear IgA bullous dermatosis (LAD) patients. In healthy controls, age had a significant impact on Ig serum concentrations: In controls at ages of 69 years or older, IgM and IgG were decreased, while all other Ig, except IgA and IgG4, were increased. When stratified by sex, lower IgM concentrations were observed in males. When corrected for age and/or sex, and compared to controls, an increase in serum IgA was noted in LAD. In almost all patient cohorts, an increase in IgG1 and IgG4 was observed, while a decrease in IgG2 or IgG3 was seen in BP or PV patients. This points toward a possible association of BP with IgG2 deficiency and warrants evaluation of IgG2 in BP patients prior to immunosuppressive therapy.
天疱疮和类天疱疮疾病是皮肤和/或黏膜的器官特异性自身免疫性疾病,由针对皮肤结构蛋白的自身抗体引起。在其他自身免疫性疾病中,已注意到原发性抗体缺陷的高患病率。相反,原发性抗体缺陷患者中自身免疫性疾病的患病率也很高。除了一项研究指出天疱疮患者IgG降低且IgG4相对富集外,天疱疮和类天疱疮患者的血清免疫球蛋白(Ig)浓度尚未得到研究。因此,我们在此旨在研究天疱疮和类天疱疮患者以及健康对照者血清中IgM、IgA、IgG和IgG1 - 4的浓度。通过酶联免疫吸附测定法(ELISA)测定了105名健康对照者、100名寻常型天疱疮(PV)患者、100名落叶型天疱疮患者、99名大疱性类天疱疮(BP)患者和55名线状IgA大疱性皮肤病(LAD)患者的血清Ig浓度。在健康对照者中,年龄对Ig血清浓度有显著影响:在69岁及以上的对照者中,IgM和IgG降低,而除IgA和IgG之外的所有其他Ig均升高。按性别分层时,男性的IgM浓度较低。在校正年龄和/或性别后,并与对照者相比,LAD患者的血清IgA升高。在几乎所有患者队列中,均观察到IgG1和IgG4升高,而BP或PV患者中则出现IgG2或IgG3降低。这表明BP可能与IgG2缺乏有关,并且在免疫抑制治疗前有必要评估BP患者的IgG2。