Inaloz H Serhat, Evereklioglu C, Unal B, Kirtak N, Eralp A, Inaloz S S
Department of Dermatology, Gaziantep University Medical Faculty, Research Hospital, Tip Fakultesi Dekanligi, Kilis Yolu Uzeri, TR-27310, Gaziantep, Turkey.
J Eur Acad Dermatol Venereol. 2004 Jan;18(1):56-61. doi: 10.1111/j.1468-3083.2004.00547.x.
Behçet's syndrome is a chronic systemic immuno-inflammatory disorder affecting multiple organs with generalized vasculitis of arteries and veins. Although the aetiology is still unknown, endothelial dysfunction is one of the most prominent features in Behçet's syndrome. The skin pathergy reaction (SPR) is a non-specific hyperreactive lesion formation that is one of the major features and diagnostic criteria of the disease. It develops after 24-48 h at the site of the needle-prick, especially in the exacerbation period, and it is very similar to the erythematous papules or pustules that appear spontaneously in patients with Behçet's syndrome. Therefore, an investigation into the formation of the SPR lesion may contribute to the pathophysiology of skin lesions of this unique disorder.
To evaluate the immunological features of SPR formation by assessing the immunohistochemical staining of cell adhesion molecules and endothelial growth factor markers such as E-selectin, P-selectin and endoglin (CD 105).
Patients with Behçet's syndrome showing positive (n = 15) or negative (n = 10) SPR and 15 age- and sex-matched hospital-based healthy control subjects from a similar ethnic background were included in this study. Patients were divided into active and inactive stage by clinical findings and acute-phase reactant parameters including erythrocyte sedimentation rate (ESR) and neutrophil count. Punch biopsy specimens were obtained both from the lesion site on the forearms at 48 h and from normal skin approximately 5 cm adjacent to the SPR site. A biopsy was also obtained from the test application site in Behçet's syndrome patients with negative SPR and healthy volunteers. Biopsy specimens were then evaluated by immunohistochemical staining.
Immunohistochemical examination demonstrated a mixed inflammatory cell infiltrate around the vessels and skin appendages that extended somewhat into the deep dermis. A positive segmental staining of E-selectin and P-selectin was noted in the endothelial cells of biopsies obtained from the patients with positive SPR. A positive segmental staining of CD 105 in the endothelial cells was also observed in the same group of patients. However, the immunostaining of the same markers was found to be negative in the biopsies obtained from normal skin of SPR-positive patients, SPR-negative patients and healthy control subjects. Both acute-phase reactant levels were significantly higher in the active stage than in inactive patients or healthy controls.
Interaction of cellular adhesion molecules together with endothelial proliferation may play an important role in the formation of SPR lesions in patients with Behçet's syndrome. The involvement of the vascular endothelium in a large number of diseases including Behçet's syndrome supports the importance of vascular-specific adhesion molecules for their aetiopathogenesis.
白塞病是一种慢性全身性免疫炎症性疾病,可累及多个器官,伴有动静脉的全身性血管炎。尽管病因仍不明,但内皮功能障碍是白塞病最显著的特征之一。皮肤针刺反应(SPR)是一种非特异性的高反应性病变形成,是该疾病的主要特征和诊断标准之一。它在针刺部位24 - 48小时后出现,尤其是在病情加重期,与白塞病患者自发出现的红斑丘疹或脓疱非常相似。因此,对SPR病变形成的研究可能有助于了解这种独特疾病皮肤病变的病理生理学。
通过评估细胞黏附分子和内皮生长因子标志物(如E - 选择素、P - 选择素和内皮糖蛋白(CD 105))的免疫组化染色来评估SPR形成的免疫特征。
本研究纳入了白塞病患者,其中SPR阳性者(n = 15)和阴性者(n = 10),以及15名年龄和性别匹配、种族背景相似的医院健康对照者。根据临床症状以及包括红细胞沉降率(ESR)和中性粒细胞计数在内的急性期反应物参数,将患者分为活动期和非活动期。在48小时时从患者前臂的病变部位以及距SPR部位约5厘米的正常皮肤处获取打孔活检标本。还从SPR阴性的白塞病患者的试验应用部位和健康志愿者处获取活检标本。然后通过免疫组化染色评估活检标本。
免疫组化检查显示血管和皮肤附属器周围有混合性炎性细胞浸润,且部分延伸至真皮深层。在SPR阳性患者的活检标本中,内皮细胞可见E - 选择素和P - 选择素的节段性阳性染色。在同一组患者的内皮细胞中也观察到CD 105的节段性阳性染色。然而,在SPR阳性患者的正常皮肤、SPR阴性患者和健康对照者的活检标本中,相同标志物的免疫染色均为阴性。急性期反应物水平在活动期患者中均显著高于非活动期患者或健康对照者。
细胞黏附分子的相互作用以及内皮细胞增殖可能在白塞病患者SPR病变的形成中起重要作用。血管内皮参与包括白塞病在内的大量疾病,这支持了血管特异性黏附分子在其发病机制中的重要性。