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Significance of Autoantibodies to Ki/SL as Biomarkers for Systemic Lupus Erythematosus and Sicca Syndrome.
Mahler, Michael; Bentow, Chelsea; Aure, Mary-Ann; Fritzler, Marvin J; Satoh, Minoru.
Afiliação
  • Mahler M; Werfen Autoimmunity, San Diego, CA 92131, USA.
  • Bentow C; Werfen Autoimmunity, San Diego, CA 92131, USA.
  • Aure MA; Werfen Autoimmunity, San Diego, CA 92131, USA.
  • Fritzler MJ; Department of Medicine, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 1N4, Canada.
  • Satoh M; Department of Clinical Nursing, School of Health Sciences, University of Occupational and Environmental Health, Kitakyushu 807-8555, Japan.
J Clin Med ; 11(12)2022 Jun 20.
Article em En | MEDLINE | ID: mdl-35743599
ABSTRACT
Anti-Ki/SL antibodies were first described in 1981 and have been associated with systemic lupus erythematosus (SLE) and Sicca syndrome. Despite the long history, very little is known about this autoantibody system, and significant confusion persists. Anti-Ki/SL antibodies target a 32 kDa protein (also known as PSME3, HEL-S-283, PA28Æ´, REGÆ´, proteasome activator subunit 3), which is part of the proteasome complex. Depending on the assay used and the cohort studied, the antibodies have been reported in approximately 20% of SLE patients with high disease specificity as compared to non-connective tissue disease controls. The aim of this review is to summarize the history and key publications, and to explore future direction of anti-Ki/SL antibodies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Clin Med Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Clin Med Ano de publicação: 2022 Tipo de documento: Article