I型干扰素与抗磷脂抗体状态之间的关联在不同祖先背景之间存在差异。

Associations between type I interferon and antiphospholipid antibody status differ between ancestral backgrounds.

作者信息

Iwamoto Taro, Dorschner Jessica, Jolly Meenakshi, Huang Xiangyang, Niewold Timothy B

机构信息

Department of Medicine and Pathology, Colton Center for Autoimmunity, New York University School of Medicine, New York, USA.

Department of Immunology, Division of Rheumatology, Mayo Clinic, Rochester, Minnesota, USA.

出版信息

Lupus Sci Med. 2018 Jan 13;5(1):e000246. doi: 10.1136/lupus-2017-000246. eCollection 2018.

Abstract

OBJECTIVE

The type I interferon pathway is activated in many patients with systemic lupus erythematosus (SLE), and anti-double-stranded DNA (dsDNA) and anti-RNA binding protein autoantibodies are correlated with high interferon-α (IFNα) activity. We studied whether antiphospholipid (APL) antibodies, which should not stimulate Toll-like receptors, are also associated with high levels of IFNα activity.

METHODS

Serum IFNα activity was measured in patients with SLE using the WISH cell bioassay. IgG APL, anti-RBP and anti-dsDNA antibodies were measured in the clinical laboratory, and standard clinical cut-offs were used to define the positive results.

RESULTS

High IFNα activity was associated with anti-RBP and anti-dsDNA antibodies in all three ancestral backgrounds. Strikingly, African-American subjects with a positive APL antibody test had higher IFNα activity than those without IgG APL antibodies. This was not shared with other ancestral backgrounds. This finding was independent of other autoantibody profiles, and clinical features did not differ between IgG APL antibody positive versus negative African-American patients.

CONCLUSION

The difference in association between IFNα activity and IgG APL status between ancestral backgrounds supports differences in molecular pathogenesis. This may suggest B cell hyperactivity in the setting of type I IFN in African-Americans and could suggest ways to individualise therapy.

摘要

目的

在许多系统性红斑狼疮(SLE)患者中,I型干扰素通路被激活,抗双链DNA(dsDNA)和抗RNA结合蛋白自身抗体与高干扰素-α(IFNα)活性相关。我们研究了不应刺激Toll样受体的抗磷脂(APL)抗体是否也与高水平的IFNα活性相关。

方法

采用WISH细胞生物测定法测量SLE患者血清中的IFNα活性。在临床实验室检测IgG APL、抗RBP和抗dsDNA抗体,并使用标准临床临界值来定义阳性结果。

结果

在所有三种祖先背景中,高IFNα活性均与抗RBP和抗dsDNA抗体相关。引人注目的是,APL抗体检测呈阳性的非裔美国受试者的IFNα活性高于无IgG APL抗体的受试者。其他祖先背景未出现这种情况。这一发现独立于其他自身抗体谱,IgG APL抗体阳性与阴性的非裔美国患者的临床特征并无差异。

结论

祖先背景之间IFNα活性与IgG APL状态关联的差异支持分子发病机制的差异。这可能表明非裔美国人在I型干扰素环境中B细胞过度活跃,并可能提示个性化治疗的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12b5/5786906/1a3442422616/lupus-2017-000246f01.jpg

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