Xu L, Robinson N, Miller S D, Chan L S
Department of Dermatology, Northwestern University Medical School, 675 N. St. Clair Street, Suite 19-150, Chicago, IL 60611, USA.
Immunol Lett. 2001 Jun 1;77(2):105-11. doi: 10.1016/s0165-2478(01)00212-7.
Bullous pemphigoid is an autoimmune blistering skin disease characterized by IgG autoantibodies targeting the skin basement membrane component type XVII collagen (BPAg2). To gain understanding of the disease's induction phase, we subcutaneously immunized adult BALB/c mice with peptides of human and/or the murine-equivalent BPAg2 pathogenic NC16A domain. Female mice were injected with peptides (human, murine, or combined human and murine), or PBS control emulsified in CFA, on a four-week interval. At the fourth and subsequent immunizations, all peptide-immunized mice were given murine peptides. Two weeks after the sixth immunization, ELISA detected IgG circulating autoantibodies against self peptides in 92% (47/51) of mice immunized with murine peptides; whereas none of the preimmune sera or the sera from PBS control-immunized mice reacted to the self peptides. In four mice their autoantibodies labeled mouse skin basement membrane. Breaking B-cell tolerance to BPAg2 sets the first step in dissecting the disease's induction phase.
大疱性类天疱疮是一种自身免疫性水疱性皮肤病,其特征是IgG自身抗体靶向皮肤基底膜成分XVII型胶原蛋白(BPAg2)。为了了解该疾病的诱导阶段,我们用人类和/或鼠类等效的BPAg2致病NC16A结构域的肽对成年BALB/c小鼠进行皮下免疫。雌性小鼠每隔四周注射肽(人类、鼠类或人类和鼠类组合)或在弗氏完全佐剂中乳化的PBS对照。在第四次及后续免疫时,所有接受肽免疫的小鼠都给予鼠类肽。第六次免疫后两周,ELISA检测到在用鼠类肽免疫的小鼠中,92%(47/51)的小鼠循环中存在针对自身肽的IgG自身抗体;而免疫前血清或PBS对照免疫小鼠的血清均未与自身肽发生反应。在四只小鼠中,它们的自身抗体标记了小鼠皮肤基底膜。打破B细胞对BPAg2的耐受性是剖析该疾病诱导阶段的第一步。