Closing the serological gap: promising novel biomarkers for the early diagnosis of rheumatoid arthritis

被引:117
作者
Trouw, Leendert A. [1 ]
Mahler, Michael [2 ]
机构
[1] Leiden Univ, Med Ctr, Dept Rheumatol, Leiden, Netherlands
[2] INOVA Diagnost Inc, San Diego, CA 92131 USA
关键词
CCP; citrullinated cyclic peptide; rheumatoid arthritis; RA; autoantibodies; CYCLIC CITRULLINATED PEPTIDE; ANTI-CCP; RHEUMATOLOGY/EUROPEAN LEAGUE; CLASSIFICATION CRITERIA; AMERICAN-COLLEGE; ANTIBODIES; AUTOANTIBODIES; VIMENTIN; PROTEINS; RA;
D O I
10.1016/j.autrev.2012.05.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by inflammation and damage of the joints affecting about 0.5% of the general population. Early treatment in RA is important as it can prevent disease progression and irreversible damage of the joints. Despite the high diagnostic value of anti-citrullinated protein antibodies (ACPA) and rheumatoid factor (RF), there is a strong demand for novel serological biomarkers to further improve the diagnosis of this abundant disease. During the last decades, several autoantigens have been described in RA including Ra33 (hnRNP A2), fibrinogen, fibronectin, alpha-enolase, type II collagen, immunoglobulin binding protein (BiP), annexins and viral citrullinated peptide (VCP) derived from Epstein Barr Virus-encoded protein (EBNA-2). More recent discoveries include antibodies to carbamylated antigens (anti-Carp), to peptidyl arginine deiminase type 4 (PAD4), to BRAF (v raf murine sarcoma viral oncogene homologue B1) and to 14 autoantigens identified by phage display technology. This review provides a current overview of novel biomarkers for RA and discusses their future potential to improve the diagnosis of the disease. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:318 / 322
页数:5
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