Biomarkers for systemic lupus erythematosus

被引:63
作者
Ahearn, Joseph M. [1 ]
Liu, Chau-Ching
Kao, Amy H.
Manzi, Susan
机构
[1] Temple Univ, Sch Med, Allegheny Singer Res Inst, Pittsburgh, PA 15212 USA
关键词
B-LYMPHOCYTE STIMULATOR; GELATINASE-ASSOCIATED LIPOCALIN; GLUTAMATE-RECEPTOR ANTIBODIES; INTERFERON REGULATORY FACTOR-5; TYROSINE-PHOSPHATASE PTPN22; MONITORING DISEASE-ACTIVITY; ANTI-NUCLEOSOME ANTIBODIES; INDUCIBLE GENE-EXPRESSION; COMPLEMENT COMPONENT C4; CD27(HIGH) PLASMA-CELLS;
D O I
10.1016/j.trsl.2012.01.021
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
The urgent need for lupus biomarkers was demonstrated in September 2011 during a Workshop sponsored by the Food and Drug Administration: Potential Biomarkers Predictive of Disease Flare. After 2 days of discussion and more than 2 dozen presentations from thought leaders in both industry and academia, it became apparent that highly sought biomarkers to predict lupus flare have not yet been identified. Even short of the elusive biomarker of flare, few biomarkers for systemic lupus erythematosus (SLE) diagnosis, monitoring, and stratification have been validated and employed for making clinical decisions. This lack of reliable, specific biomarkers for SLE hampers proper clinical management of patients with SLE and impedes development of new lupus therapeutics. As such, the intensity of investigation to identify lupus biomarkers is climbing a steep trajectory, lending cautious optimism that a validated panel of biomarkers for lupus diagnosis, monitoring, stratification, and prediction of flare may soon be in hand. (Translational Research 2012;159:326-342)
引用
收藏
页码:326 / 342
页数:17
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