The Garvan Institute of Medical Research, Darlinghurst, and St. Vincent's Clinical School, Faculty of Medicine, UNSW Sydney, Australia.
Department of Rheumatology and Clinical Immunology, University of Groningen, University Medical Center Groningen, The Netherlands, and Immunology Division, Walter and Eliza Hall Institute for Medical Research, Parkville, Australia.
Clin Exp Rheumatol. 2020 Jul-Aug;38 Suppl 126(4):271-282. Epub 2020 Sep 22.
Primary Sjögren's syndrome (pSS) is often considered a B cell-mediated disease, yet the precise role of B cells in the pathogenesis is not fully understood. This is exemplified by the failure of multiple clinical trials directed at B cell depletion or inhibition. To date, most prognostic markers for severe disease outcomes are autoantibodies, but the underlying mechanisms by which B cells drive diverse disease presentations in pSS likely extend beyond autoantibody production. Here we outline an expanded role of B cells in disease pathogenesis drawing on examples from animal models of SS, and from other autoimmune diseases that share similar clinical or immunological abnormalities. We focus on recent findings from the detailed analysis of pathogenic B cells in patients with pSS to propose strategies for patient stratification to improve clinical trial outcomes. We conclude that an integrated cellular, molecular and genetic analysis of patients with pSS will reveal the underlying pathogenic mechanisms and guide precision medicine.
原发性干燥综合征(pSS)通常被认为是一种 B 细胞介导的疾病,但 B 细胞在发病机制中的确切作用尚不完全清楚。这一点可以从针对 B 细胞耗竭或抑制的多项临床试验的失败中得到证明。迄今为止,大多数严重疾病结局的预后标志物都是自身抗体,但 B 细胞在 pSS 中导致不同疾病表现的潜在机制可能超出了自身抗体的产生。在这里,我们借鉴 SS 动物模型和具有相似临床或免疫异常的其他自身免疫性疾病的例子,概述了 B 细胞在疾病发病机制中的扩展作用。我们专注于对 pSS 患者致病性 B 细胞的详细分析的最新发现,提出了对患者进行分层的策略,以改善临床试验结果。我们得出结论,对 pSS 患者进行细胞、分子和遗传的综合分析将揭示潜在的发病机制,并指导精准医学。