New York University Grossman School of Medicine, Department of Medicine, New York, NY, USA.
New York University Grossman School of Medicine, Department of Medicine, New York, NY, USA; New York University Grossman School of Medicine, Department of Pathology, USA; New York University Grossman School of Medicine, Department of Medicine Division of Rheumatology, NYU Langone Ocular Rheumatology Program, New York, NY, USA; New York University Grossman School of Medicine, Department of Medicine, Division of Rheumatology, NYU Langone Center for Behçet's Disease, New York, NY, USA.
Best Pract Res Clin Rheumatol. 2024 May;38(2):101977. doi: 10.1016/j.berh.2024.101977. Epub 2024 Jul 31.
Human leukocyte antigen (HLA) class I association is a well-established feature of common and uncommon inflammatory diseases, but it is unknown whether it impacts the pathogenesis of these disorders. The "arthritogenic peptide" hypothesis proposed initially for HLA-B27-associated ankylosing spondylitis (AS) seems the most intuitive to serve as a model for other HLA class I-associated diseases, but evidence supporting it has been scarce. Recent technological advances and the discovery of epistatic relationships between disease-associated HLA class I and endoplasmic reticulum aminopeptidase (ERAP) coding variants have led to the generation of new data and conceptual approaches to the problem requiring its re-examination. Continued success in these endeavors holds promise to resolve a Gordian Knot in human immunobiology. It may ultimately benefit patients by enabling the development of new therapies and precision tools for assessing disease risk and predicting treatment responses.
人类白细胞抗原 (HLA) Ⅰ类关联是常见和罕见炎症性疾病的一个既定特征,但尚不清楚它是否影响这些疾病的发病机制。最初提出的用于 HLA-B27 相关强直性脊柱炎 (AS) 的“关节炎肽”假说似乎是最直观的 HLA Ⅰ类相关疾病模型,但支持它的证据很少。最近的技术进步和发现与疾病相关的 HLA Ⅰ类和内质网氨肽酶 (ERAP) 编码变异体之间的上位性关系,导致了对该问题的重新审视,产生了新的数据和概念方法。这些努力的持续成功有望解决人类免疫生物学中的一个棘手问题。它最终可能通过开发新的治疗方法和精确的工具来评估疾病风险和预测治疗反应,使患者受益。