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人大疱性类天疱疮抗原2转基因皮肤在野生型小鼠中引发特异性IgG。

Human bullous pemphigoid antigen 2 transgenic skin elicits specific IgG in wild-type mice.

作者信息

Olasz Edit B, Roh Jooyoung, Yee Carole L, Arita Ken, Akiyama Masashi, Shimizu Hiroshi, Vogel Jonathan C, Yancey Kim B

机构信息

Department of Dermatology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

出版信息

J Invest Dermatol. 2007 Dec;127(12):2807-17. doi: 10.1038/sj.jid.5700970. Epub 2007 Jul 26.

Abstract

Bullous pemphigoid antigen 2 (BPAG2) is targeted by autoantibodies in patients with bullous pemphigoid (BP), and absent in patients with one type of epidermolysis bullosa (OMIM #226650). A keratin 14 promoter construct was used to produce transgenic (Tg) mice appropriately expressing human BPAG2 (hBPAG2) in murine epidermal basement membrane (BM). Grafts of Tg skin placed on gender-matched, syngeneic wild type (Wt) or major histocompatibility complex I (MHC I)-/- mice elicited IgG that bound human epidermal BM and BPAG2. Production of such IgG in grafted mice was prompt (detectable within 16+/-2 days), robust (titer > or = 1,280), durable (present > or = 380 days), and correlated with the involution and loss of Tg skin grafts. MHC II-/- mice grafted with Tg skin did not develop anti-hBPAG2 IgG or graft loss indicating that MHC II:CD4+ T cell interactions were crucial for these responses. Tg skin grafts on Wt mice developed neutrophil-rich infiltrates, dermal edema, subepidermal blisters, and deposits of immunoreactants in epidermal BM. This model shows fidelity to alterations seen in patients with BP, has relevance to immune responses that may arise in patients with epidermolysis bullosa following BPAG2 gene replacement, and can be used to identify interventions that may block production of IgG against proteins in epidermal BM.

摘要

大疱性类天疱疮抗原2(BPAG2)是大疱性类天疱疮(BP)患者自身抗体的靶抗原,在一种遗传性大疱性表皮松解症患者(OMIM #226650)中缺失。利用角蛋白14启动子构建体产生在小鼠表皮基底膜(BM)中适当表达人BPAG2(hBPAG2)的转基因(Tg)小鼠。将Tg皮肤移植到性别匹配的同基因野生型(Wt)或主要组织相容性复合体I(MHC I)基因敲除小鼠上,可诱导产生结合人表皮BM和BPAG2的IgG。移植小鼠中这种IgG的产生迅速(在16±2天内可检测到)、强烈(滴度≥1280)、持久(存在≥380天),并与Tg皮肤移植的退化和丢失相关。移植了Tg皮肤的MHC II基因敲除小鼠未产生抗hBPAG2 IgG或移植丢失,表明MHC II:CD4 + T细胞相互作用对这些反应至关重要。Wt小鼠上的Tg皮肤移植出现富含中性粒细胞的浸润、真皮水肿、表皮下水疱以及表皮BM中免疫反应物的沉积。该模型显示出与BP患者所见改变的一致性,与BPAG2基因替代后遗传性大疱性表皮松解症患者可能出现的免疫反应相关,并且可用于确定可能阻断针对表皮BM中蛋白质的IgG产生的干预措施。

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