Department of Dermatology, University Medical Center Freiburg, Germany.
J Eur Acad Dermatol Venereol. 2010 May;24(5):587-94. doi: 10.1111/j.1468-3083.2009.03480.x. Epub 2009 Nov 2.
Graft-versus-host disease (GvHD) occurs frequently after haematopoietic cell transplantation (HCT). Mucocutaneous lesions of GvHD may mimic bullous autoimmune dermatoses, and 10 cases of concurrent GvHD and a bullous autoimmune disease have been reported in the literature.
To determine the frequency of circulating antibodies to the cutaneous basement membrane zone (BMZ) in HCT patients with GvHD in comparison with HCT patients without GvHD, psoriasis patients and healthy controls.
We examined 42 patients with chronic GvHD, 18 HCT patients without GvHD, 11 psoriasis patients and 40 healthy controls, prospectively. Sera were tested by indirect immunofluorescence (IIF) on salt-split skin, NC16a-ELISA and immunoblot using keratinocyte extracts. Univariate statistical analyses and logistic regression were performed to assess possible correlations of graft and patient characteristics with the presence of BMZ antibodies.
Circulating basement membrane zone (BMZ) antibodies were detected in 10/42 (24%) GvHD sera by immunoblot, but not in any of the HCT sera from patients without GvHD (0/18; 0%). The antibodies targeted collagen VII, BP230, collagen XVII/BP180 or p200/laminin gamma1. Clinically manifest bullous autoimmune dermatoses (bullous pemphigoid or epidermolysis bullosa acquisita) were found in two GvHD patients. 1/11 (9%) psoriasis sera and 1/40 (2.4%) healthy control sera reacted with collagen XVII or BP230, respectively.
Circulating BMZ antibodies are significantly associated with chronic GvHD in contrast to uncomplicated HCT. Recurrent mucocutaneous lesions in chronic inflammatory skin disorders may liberate antigens, which may lead to production of BMZ antibodies, particularly in the context of GvHD-mediated reduced self-tolerance.
造血细胞移植(HCT)后常发生移植物抗宿主病(GvHD)。GvHD 的黏膜皮肤损害可能类似于大疱自身免疫性皮肤病,文献中已有 10 例同时发生 GvHD 和大疱自身免疫性疾病的报道。
与未发生 GvHD 的 HCT 患者、银屑病患者和健康对照者相比,确定 HCT 患者发生 GvHD 时循环抗皮肤基底膜带(BMZ)抗体的频率。
我们前瞻性地检测了 42 例慢性 GvHD 患者、18 例未发生 GvHD 的 HCT 患者、11 例银屑病患者和 40 例健康对照者的血清。通过间接免疫荧光(IIF)在盐裂皮肤、NC16a-ELISA 和使用角质形成细胞提取物的免疫印迹上检测血清。采用单变量统计分析和逻辑回归评估移植物和患者特征与 BMZ 抗体存在的可能相关性。
免疫印迹检测到 10/42(24%)GvHD 血清中存在循环 BMZ 抗体,但未在任何未发生 GvHD 的 HCT 患者血清中检测到(0/18)。这些抗体靶向胶原 VII、BP230、胶原 XVII/BP180 或 p200/层粘连蛋白γ1。在 2 例 GvHD 患者中发现了临床表现为大疱自身免疫性皮肤病(大疱性类天疱疮或获得性大疱性表皮松解症)。1/11(9%)银屑病血清和 1/40(2.4%)健康对照血清分别与胶原 XVII 或 BP230 反应。
与单纯 HCT 相比,循环 BMZ 抗体与慢性 GvHD 显著相关。慢性炎症性皮肤病的复发性黏膜皮肤病变可能释放抗原,这可能导致 BMZ 抗体的产生,特别是在 GvHD 介导的自身耐受性降低的情况下。