Department of Rheumatology and Clinical Immunology, University Medical Center Freiburg, Freiburg, Germany.
PLoS One. 2010 May 26;5(5):e10838. doi: 10.1371/journal.pone.0010838.
Stiff person syndrome (SPS) is a rare, neurological disorder characterized by sudden cramps and spasms. High titers of enzyme-inhibiting IgG autoantibodies against the 65 kD isoform of glutamic acid decarboxylase (GAD65) are a hallmark of SPS, implicating an autoimmune component in the pathology of the syndrome. Studying the B cell compartment and the anti-GAD65 B cell response in two monozygotic twins suffering from SPS, who were treated with the B cell-depleting monoclonal anti-CD20 antibody rituximab, we found that the humoral autoimmune response in SPS is composed of a rituximab-sensitive part that is rapidly cleared after treatment, and a rituximab-resistant component, which persists and acts as a reservoir for autoantibodies inhibiting GAD65 enzyme activity. Our data show that these potentially pathogenic anti-GAD65 autoantibodies are secreted by long-lived plasma cells, which may either be persistent or develop from rituximab-resistant memory B lymphocytes. Both subsets represent only a fraction of anti-GAD65 autoantibody secreting cells. Therefore, the identification and targeting of this compartment is a key factor for successful treatment planning of SPS and of similar autoimmune diseases.
僵人综合征(SPS)是一种罕见的神经疾病,其特征是突然出现痉挛和抽搐。谷氨酸脱羧酶(GAD)65 酶抑制性 IgG 自身抗体的高滴度是 SPS 的标志,表明该综合征的病理学存在自身免疫成分。在患有 SPS 的一对同卵双胞胎中,研究 B 细胞区室和抗 GAD65 B 细胞反应,他们接受了 B 细胞耗竭性单克隆抗 CD20 抗体利妥昔单抗治疗,我们发现 SPS 中的体液自身免疫反应由利妥昔单抗敏感部分组成,该部分在治疗后迅速清除,还有利妥昔单抗抗性成分,它持续存在并作为抑制 GAD65 酶活性的自身抗体的储存库。我们的数据表明,这些潜在致病性的抗 GAD65 自身抗体由长寿浆细胞分泌,这些浆细胞可能是持续存在的,也可能是由利妥昔单抗抗性记忆 B 淋巴细胞发展而来的。这两个亚群仅代表分泌抗 GAD65 自身抗体的细胞的一部分。因此,该细胞亚群的鉴定和靶向是成功治疗 SPS 和类似自身免疫性疾病的关键因素。