Candidate autoantibodies for primary Sjogren's syndrome: where are they now?

被引:0
作者
He, J. [1 ,2 ]
Jiang, J. [3 ,4 ,5 ]
Baumgart, K. [2 ]
机构
[1] Concord Repatriat Gen Hosp, Dept Rheumatol, Sydney, Australia
[2] Son Hlth, Dept Immunol, Douglass Hanly Moir Pathol, Macquarie Pk, Australia
[3] Blacktown Hosp, Dept Immunol, Blacktown, Australia
[4] Univ Sydney, Sch Med, Sydney, Australia
[5] Univ Western Sydney, Blacktown Clin Sch, Sch Med, Penrith, Australia
关键词
Sjogren's syndrome; autoantibodies; biomarkers; ALPHA-FODRIN ANTIBODIES; CLASSIFICATION CRITERIA; RECEPTOR AUTOANTIBODIES; COGNITIVE DYSFUNCTION; AMERICAN-COLLEGE; SEVERE DISEASE; DATA-DRIVEN; DIAGNOSIS; PROTEIN; IDENTIFICATION;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although ANA, SSA and SSB antibody testing are universally accepted biomarkers for Sjogren's syndrome (SS) diagnosis, they do not occur in all patients. Up to 18% of SS patients are seronegative, with potential for delayed or missed diagnosis. There are no clinically available autoantibodies with predictive value for SS end-organ complications. Over the last three decades, novel autoantibodies for SS diagnosis and monitoring have been identified but few have transitioned from research studies to clinical use. We performed a literature review of candidate serum autoantibodies to examine their persistence in the literature and potential clinical utility. Of the nineteen autoantibodies we identified, AQP5, SP-1, CA6, and PSP Abs have the most promise. Larger cohort studies are needed to determine their potential contribution in SS management.
引用
收藏
页码:2387 / 2394
页数:8
相关论文
共 66 条
[11]   New autoantibody detection technologies yield novel insights into autoimmune disease [J].
Burbelo, Peter D. ;
O'Hanlon, Terrance P. .
CURRENT OPINION IN RHEUMATOLOGY, 2014, 26 (06) :717-723
[12]  
Cafaro G, 2020, CLIN EXP RHEUMATOL, V38, pS53
[13]  
Chatzis LG, 2021, CLIN EXP RHEUMATOL, V39, pS80, DOI 10.55563/clinexprheumatol/47a4kr
[14]   Investigation of three potential autoantibodies in Sjogren's syndrome and associated MALT lymphoma [J].
Cui, Li ;
Elzakra, Naseim ;
Xu, Shuaimei ;
Xiao, Gary Guishan ;
Yang, Yan ;
Hu, Shen .
ONCOTARGET, 2017, 8 (18) :30039-30049
[15]   Meta-Analysis of Anti-Muscarinic Receptor Type 3 Antibodies for the Diagnosis of Sjogren Syndrome [J].
Deng, Chuiwen ;
Hu, Chaojun ;
Chen, Si ;
Li, Jing ;
Wen, Xiaoting ;
Wu, Ziyan ;
Li, Yuan ;
Zhang, Fengchun ;
Li, Yongzhe .
PLOS ONE, 2015, 10 (01)
[16]   Autoantibodies binding to stathmin-4: new marker for polyneuropathy in primary Sjogren's syndrome [J].
Duda, Sabrina ;
Witte, Torsten ;
Stangel, Martin ;
Adams, Jan ;
Schmidt, Reinhold E. ;
Baerlecken, Niklas T. .
IMMUNOLOGIC RESEARCH, 2017, 65 (06) :1099-1102
[17]   PUF60: a prominent new target of the autoimmune response in dermatomyositis and Sjogren's syndrome [J].
Fiorentino, David F. ;
Presby, Matthew ;
Baer, Alan N. ;
Petri, Michelle ;
Rieger, Kerri E. ;
Soloski, Mark ;
Rosen, Antony ;
Mammen, Andrew L. ;
Christopher-Stine, Lisa ;
Casciola-Rosen, Livia .
ANNALS OF THE RHEUMATIC DISEASES, 2016, 75 (06) :1145-1151
[18]  
Galloway James N., SCIENCE, V320, P889, DOI [10.1126/science.3529391, DOI 10.1126/SCIENCE.3529391, 10.1126/science.1136674, DOI 10.1126/SCIENCE.1195403]
[19]   Recent Advances in Mouse Models of Sjogren's Syndrome [J].
Gao, Yunzhen ;
Chen, Yan ;
Zhang, Zhongjian ;
Yu, Xinhua ;
Zheng, Junfeng .
FRONTIERS IN IMMUNOLOGY, 2020, 11
[20]   Anti-DNase I Antibody A New Serological Reactivity in Primary Sjogren Syndrome [J].
Griffo, Priscilla ;
Viana, Vilma V. S. T. ;
Pasoto, Sandra G. ;
Leon, Elaine P. ;
Bonfa, Eloisa .
JCR-JOURNAL OF CLINICAL RHEUMATOLOGY, 2020, 26 (01) :19-23