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Reactivity against the Five Domains of and#946;<sub>2</sub> Glycoprotein I: A Focus on Systemic Lupus Erythematosus | OMICS International | Abstract
ISSN: 2155-9899

Journal of Clinical & Cellular Immunology
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Review Article

Reactivity against the Five Domains of β2 Glycoprotein I: A Focus on Systemic Lupus Erythematosus

Cecilia Beatrice Chighizola1,2, Maria Orietta Borghi1, Claudia Grossi1, Francesca Pregnolato1, Maria Gerosa2 and Pier Luigi Meroni1,2*
1Immunorheumatological Research Laboratory, Istituto Auxologico Italiano, Milan, Italy
2Department of Clinical Sciences and Community Health, University of Milan, Milan, Italy
Corresponding Author : Pier Luigi Meroni
Department of Rheumatology – Istituto G. Pini
Piazza C. Ferrari, 1 – 20122 Milano, Italy
Tel: +390258296272
Fax: +390258296315
E-mail: [email protected]
Received March 03, 2014; Accepted April 03, 2014; Published April 09, 2014
Citation: Chighizola CB, Borghi MO, Grossi C, Pregnolato F, Gerosa M, et al. (2014) Reactivity against the Five Domains of β2 Glycoprotein I: A Focus on Systemic Lupus Erythematosus. J Clin Cell Immunol 5:206. doi: 0.4172/2155-9899.1000206
Copyright: © 2014 Chighizola CB, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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Abstract

Beta-2 glycoprotein I (β2GPI) is the main antigenic target for antiphospholipid antibodies (aPL), the serological markers of antiphospholipid syndrome (APS), a systemic autoimmune disease characterized by vascular thrombosis and/or pregnancy morbidity. aPL are detected in 20 to 50% of patients with systemic lupus erythematosus (SLE), representing a poor prognostic factor. Indeed, thrombotic events heralds high morbidity and mortality, being regarded as the strongest predictors of death in the first five years after SLE onset. It would be thus very important to identify a reliable laboratory tool such as anti-domain antibodies to better risk-stratify lupus patients according to the aPL profile, in order to tailor treatment strategies. Domain I (DI) of β2GPI has lately been identified as the main epitope targeted by antibodies reacting against β2GPI isolated from APS patients, well correlating with thrombotic as well as obstetric manifestations. Interestingly, anti-DI antibodies have been shown to well correlate with lupus anticoagulant and to predict the clinical manifestations of the syndrome, thrombotic events as well as pregnancy complications. Further, anti-DI antibodies allow to identify patients at highest clinical risk, presenting a good specificity for APS. On the other hand, anti- β2GPI antibodies from aPL asymptomatic carriers or subjects with infectious diseases preferentially display reactivity towards DIV or DV of the molecule.
Few studies have to date evaluated the domain profile of anti-β2GPI antibodies in subjects with SLE, even though it would be very relevant from a clinical point of view to understand whether among patients with SLE the domain specificities of anti-β2GPI antibodies display a clinical meaning comparable to the one they exert in APS. It is therefore rather appropriate to review the available evidence about anti-domain specificities with a particular focus on SLE.

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