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脊柱关节炎:处于免疫交叉路口的疾病。

Spondyloarthropathy: disease at the crossroads of immunity.

作者信息

FitzGerald Oliver, McInnes Iain

机构信息

St. Vincent's University Hospital, Elm Park, Dublin, 4, Ireland.

出版信息

Best Pract Res Clin Rheumatol. 2006 Oct;20(5):949-67. doi: 10.1016/j.berh.2006.06.010.

Abstract

Up until recently, the prevailing paradigm relating to spondyloarthropathy (SpA) pathogenesis was that they were human leukocyte antigen (HLA)-associated, T-cell-driven autoimmune diseases. This view is now being questioned. Careful studies of well-characterised cohorts of patients with SpA, including detailed analysis of involved tissue, together with clinical trials of targeted treatments, in particular anti-tumour necrosis factor (TNF) therapies, have contributed enormously to both interest in and understanding of disease pathogenesis. In this chapter, our current knowledge and understanding of the relative contributions of the components of the innate and adaptive arms of the immune response to SpA pathogenesis is reviewed. It is clear that both arms of the immune response are involved and inter-dependent in SpA. With continued emphasis on discovery research, including detailed analysis of novel therapeutic interventions, significant additional breakthroughs in SpA are likely to be forthcoming.

摘要

直到最近,与脊柱关节炎(SpA)发病机制相关的主流范式一直认为,它们是与人类白细胞抗原(HLA)相关的、由T细胞驱动的自身免疫性疾病。现在这种观点正受到质疑。对特征明确的SpA患者队列进行的仔细研究,包括对受累组织的详细分析,以及靶向治疗的临床试验,特别是抗肿瘤坏死因子(TNF)疗法,极大地促进了人们对疾病发病机制的兴趣和理解。在本章中,我们回顾了目前对免疫反应的固有和适应性分支的组成部分对SpA发病机制的相对贡献的认识和理解。很明显,免疫反应的两个分支在SpA中都有涉及且相互依赖。随着对发现研究的持续重视,包括对新型治疗干预措施的详细分析,SpA很可能会有更多重大突破。

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