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Predisposing factors in the spondyloarthropathies: new insights into the role of HLA-B27.

作者信息

Colbert R A, Prahalad S

机构信息

William S. Rowe Division of Rheumatology, Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229-3039, USA.

出版信息

Curr Rheumatol Rep. 2001 Oct;3(5):404-11. doi: 10.1007/s11926-996-0011-9.

DOI:10.1007/s11926-996-0011-9
PMID:11564372
Abstract

Spondyloarthropathies represent complex genetic diseases whose development is influenced by environmental factors. Estimates suggest that three to nine loci may be responsible for the majority of the genetic susceptibility to ankylosing spondylitis. The only susceptibility locus identified to date in multiple populations is HLA-B, where several HLA-B27 alleles (subtypes) are strongly associated with disease. Recent evidence implicates cytochrome P450 2D6 as a second locus, although its influence on overall risk appears small. Despite considerable efforts to define how HLA-B27 contributes to disease, its role remains enigmatic. Increasing evidence suggests it has effects that are unrelated to its physiologic function. The basis for this is unknown but may be a consequence of the unusual tendency of this allele to misfold.

摘要

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本文引用的文献

1
Interleukin 1 gene cluster polymorphisms in multiplex families with spondylarthropathies.脊柱关节病多发家系中白细胞介素1基因簇多态性
Cytokine. 2001 Jan 21;13(2):98-103. doi: 10.1006/cyto.2000.0795.
2
Increased risk of developing ankylosing spondylitis among first-born children.
Arthritis Rheum. 2000 Dec;43(12):2818-22. doi: 10.1002/1529-0131(200012)43:12<2818::AID-ANR23>3.0.CO;2-F.
3
TAP1 and TAP2 polymorphism in Spanish patients with ankylosing spondylitis.
Exp Clin Immunogenet. 2000;17(4):199-204. doi: 10.1159/000019139.
4
Recurrence risk modelling of the genetic susceptibility to ankylosing spondylitis.强直性脊柱炎遗传易感性的复发风险建模
Ann Rheum Dis. 2000 Nov;59(11):883-6. doi: 10.1136/ard.59.11.883.
5
Development of spontaneous arthritis in beta2-microglobulin-deficient mice without expression of HLA-B27: association with deficiency of endogenous major histocompatibility complex class I expression.在不表达HLA - B27的β2 - 微球蛋白缺陷小鼠中自发性关节炎的发生:与内源性主要组织相容性复合体I类表达缺陷相关
Arthritis Rheum. 2000 Oct;43(10):2290-6. doi: 10.1002/1529-0131(200010)43:10<2290::AID-ANR17>3.0.CO;2-6.
6
IRE1 and efferent signaling from the endoplasmic reticulum.内质网应激反应激酶1(IRE1)与内质网的传出信号传导
J Cell Sci. 2000 Nov;113 Pt 21:3697-702. doi: 10.1242/jcs.113.21.3697.
7
The HLA-B*2709 subtype in a patient with undifferentiated spondarthritis.一名未分化脊柱关节炎患者中的HLA - B*2709亚型
Ann Rheum Dis. 2000 Aug;59(8):654-5. doi: 10.1136/ard.59.8.654a.
8
MICA gene triplet repeat polymorphism in patients with HLA-B27 positive and negative ankylosing spondylitis from Sardinia.来自撒丁岛的 HLA - B27 阳性和阴性强直性脊柱炎患者的 MICA 基因三联体重复多态性
J Rheumatol. 2000 Sep;27(9):2193-7.
9
Toll-like receptors in the induction of the innate immune response.Toll样受体在天然免疫应答的诱导过程中。
Nature. 2000 Aug 17;406(6797):782-7. doi: 10.1038/35021228.
10
Modification of disease outcome in Salmonella-infected patients by HLA-B27.HLA - B27对沙门氏菌感染患者疾病转归的影响
Arthritis Rheum. 2000 Jul;43(7):1527-34. doi: 10.1002/1529-0131(200007)43:7<1527::AID-ANR17>3.0.CO;2-G.