Department of Dermatology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama City, Okayama 700-8558, Japan.
Br J Dermatol. 2012 Aug;167(2):252-61. doi: 10.1111/j.1365-2133.2012.10929.x. Epub 2012 Jun 11.
Antidesmoglein (anti-Dsg) 3 serum antibody titres are usually correlated with the disease activity of pemphigus vulgaris (PV), but some patients retain high titres even in remission.
The aim of our study was to determine whether anti-Dsg3 antibodies in PV sera recognized calcium (Ca(2+) )-dependent or non-Ca(2+) -dependent epitopes, and to evaluate their pathogenicity.
Dsg3 baculoprotein-coated enzyme-linked immunosorbent assay (ELISA) plates were treated with 0.5 mmol L(-1) ethylenediaminetetraacetic acid (EDTA). The binding ability of anti-Dsg3 monoclonal antibodies (mAbs) was analysed. Eight of the 83 patients with PV who were screened had elevated Dsg3 ELISA index values > 00 in remission. The binding ability of these PV sera was analysed. We evaluated the pathogenicity of anti-Dsg3 serum antibodies against the non-Ca(2+) -dependent epitopes using a dissociation assay.
The reactivity of pathogenic anti-Dsg3 mAbs against the Ca(2+) -dependent epitopes diminished markedly in the EDTA-treated ELISA, whereas no such reduction was observed in mAbs against the non-Ca(2+) -dependent epitopes. The sera of all the patients contained antibodies against both Ca(2+) -dependent and non-Ca(2+) -dependent epitopes. In six out of the eight patients, the ratio of antibodies against Ca(2+) -dependent to non-Ca(2+) -dependent epitopes decreased in remission. EDTA-treated Dsg3 baculoproteins adsorbed anti-Dsg3 serum antibodies against the non-Ca(2+) -dependent epitopes, but the remnant PV antibodies retained the ability to induce acantholysis in the dissociation assay.
We have established an assay to measure indirectly the titres of anti-Dsg3 serum antibodies against the Ca(2+) -dependent epitopes, based on the differences between EDTA-untreated and EDTA-treated ELISA index values, as a routine laboratory test to reflect the pathogenic anti-Dsg3 serum antibody titres more accurately.
抗桥粒芯糖蛋白 3(anti-Dsg)3 血清抗体滴度通常与寻常型天疱疮(PV)的疾病活动相关,但一些患者在缓解期仍保留高滴度。
本研究旨在确定 PV 血清中的抗 Dsg3 抗体是否识别钙(Ca2+)依赖性或非 Ca2+依赖性表位,并评估其致病性。
用 0.5mmol/L 乙二胺四乙酸(EDTA)处理 Dsg3 杆状病毒包被的酶联免疫吸附试验(ELISA)板。分析抗 Dsg3 单克隆抗体(mAb)的结合能力。在筛选的 83 例 PV 患者中,有 8 例在缓解期的 Dsg3 ELISA 指数值>00 升高。分析这些 PV 血清的结合能力。我们使用解离试验评估抗 Dsg3 血清抗体针对非 Ca2+依赖性表位的致病性。
致病性抗 Dsg3 mAb 对 Ca2+依赖性表位的反应性在 EDTA 处理的 ELISA 中显著减弱,而对非 Ca2+依赖性表位的 mAb 则无此减少。所有患者的血清均含有针对 Ca2+依赖性和非 Ca2+依赖性表位的抗体。在 8 例患者中,有 6 例患者在缓解期时针对 Ca2+依赖性表位的抗体与非 Ca2+依赖性表位的抗体比值降低。EDTA 处理的 Dsg3 杆状病毒蛋白吸附针对非 Ca2+依赖性表位的抗 Dsg3 血清抗体,但残留的 PV 抗体在解离试验中仍保留诱导棘层松解的能力。
我们建立了一种间接测量抗 Dsg3 血清抗体针对 Ca2+依赖性表位的滴度的测定方法,该方法基于 EDTA 未处理和 EDTA 处理 ELISA 指数值之间的差异,作为一种常规实验室检测方法,可更准确地反映致病性抗 Dsg3 血清抗体滴度。