Grunebaum E, Blank M, Cohen S, Afek A, Kopolovic J, Meroni P L, Youinou P, Shoenfeld Y
Centre for Autoimmune Diseases, Department of Medicine B, Tel-Hashomer, Israel.
Clin Exp Immunol. 2002 Nov;130(2):233-40. doi: 10.1046/j.1365-2249.2002.02000.x.
Kawasaki disease (KD) is a systemic vasculitis with cardiac and noncardiac complications. Anti--endothelial cell antibodies (AECA) are found among many patients with KD. The aim of this study was to investigate the pathogenic role of AECA in KD using in vitro and in vivo experimental models. F(ab)2 fragments of IgG-AECA and IgM-AECA were affinity purified from a patient with active KD. Their endothelial binding and ability to induce a pro-adhesive and a pro-inflammatory phenotype were evaluated in vitro. Twenty Balb/C mice were immunized with KD-AECA or with control Ig (N-Ig) to induce AECA in a murine model by the idiotypic manipulation method. Both KD-AECA isotypes bind significantly to human umbilical vein endothelial cell (HUVEC) compared to N-Ig. The in vitro activity was demonstrated by the antibodies ability to activate endothelial cells resulting in increased IL-6 secretion, adhesion molecule expression and monocytic cell line (U937) adherence to HUVEC. Five of the mice that received KD-AECA developed murine AECA after 3 months. None of the mice that received N-Ig produced AECA. The murine AECA increased monocyte adhesion to EC in vitro, similarly to the AECA used for immunization. Furthermore, all the mice that developed AECA had proteinuria and IgG deposition in the renal mesangium. No histological or immunofluorescence evidence of cardiac vasculitis could be detected. AECA might play a role in the emergence of some of KD manifestations.
川崎病(KD)是一种伴有心脏和非心脏并发症的系统性血管炎。许多KD患者体内可检测到抗内皮细胞抗体(AECA)。本研究旨在利用体外和体内实验模型探讨AECA在KD发病机制中的作用。从一名活动期KD患者体内亲和纯化出IgG-AECA和IgM-AECA的F(ab)2片段。体外评估它们与内皮细胞的结合能力以及诱导促黏附及促炎表型的能力。采用独特型操纵法,用KD-AECA或对照Ig(N-Ig)免疫20只Balb/C小鼠,在小鼠模型中诱导产生AECA。与N-Ig相比,两种KD-AECA亚型均能与人脐静脉内皮细胞(HUVEC)显著结合。抗体激活内皮细胞的能力证明了其体外活性,这导致白细胞介素-6分泌增加、黏附分子表达增加以及单核细胞系(U937)黏附于HUVEC。5只接受KD-AECA免疫的小鼠在3个月后产生了鼠源性AECA。接受N-Ig免疫的小鼠均未产生AECA。鼠源性AECA在体外增加了单核细胞与内皮细胞的黏附,类似于用于免疫的AECA。此外,所有产生AECA的小鼠均出现蛋白尿,且肾系膜中有IgG沉积。未检测到心脏血管炎的组织学或免疫荧光证据。AECA可能在KD某些临床表现的发生中起作用。