dc.creatorWeiss R.
dc.creatorBitton A.
dc.creatorNahary L.
dc.creatorArango M.T.
dc.creatorBenhar I.
dc.creatorBlank M.
dc.creatorShoenfeld Y.
dc.creatorChapman J.
dc.date.accessioned2020-05-26T00:11:04Z
dc.date.accessioned2022-09-22T14:32:57Z
dc.date.available2020-05-26T00:11:04Z
dc.date.available2022-09-22T14:32:57Z
dc.date.created2020-05-26T00:11:04Z
dc.identifier0257277X
dc.identifierhttps://repository.urosario.edu.co/handle/10336/24279
dc.identifierhttps://doi.org/10.1007/s12026-016-8840-8
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3439889
dc.description.abstractAntiphospholipid syndrome (APS) affects coagulation and the brain by autoimmune mechanisms. The major antigen in APS is beta-2-glycoprotein I (?2-GPI) is known to complex with annexin A2 (ANXA2), and antibodies to ANXA2 have been described in APS. We measured these antibodies in mice with experimental APS (eAPS) induced by immunization with ?2-GPI. Sera of these mice reacted significantly with recombinant ANXA2 by enzyme-linked immunosorbent assay (ELISA) and the eAPS mice had significantly high levels of immunoglobulin G (IgG) in the brain by immunoblot assays compared to adjuvant immunized controls. Immunoprecipitation performed by mixing eAPS brain tissue with protein-G beads resulted in identification of two autoantigens unique to the eAPS group, one of which was ANXA2. In order to study more directly and methodically the specific role of anti-ANXA2 antibodies in APS, we immunized mice with ?2-GPI which contained no ANXA2 or with ANXA2 and measured antibodies to these proteins. Levels of antibodies to ANXA2 measured by ELISA were 0.72 ± 0.007 arbitrary units (a.u), 0.24 ± 0.03 and 0.02 ± 0.01 a.u for sera from ANXA2, ?2-GPI and control mice, respectively (p  less than  0.0001 and p = 0.037 for the comparison of the ANXA2 and ?2-GPI groups to the controls). Purified IgG from ?2-GPI sera did not show cross-binding with ANXA2. Antibodies to ?2-GPI and phospholipids were found in the ?2-GPI immunized group only. The present study suggests an immune response to the ?2-GPI–ANXA2 complex in eAPS and provides a novel ANXA2 immunization model which will serve to study the role of ANXA2 antibodies in of APS. © 2016, Springer Science+Business Media New York.
dc.languageeng
dc.publisherHumana Press Inc.
dc.relationImmunologic Research, ISSN:0257277X, Vol.65, No.1 (2017); pp. 355-362
dc.relationhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84979633320&doi=10.1007%2fs12026-016-8840-8&partnerID=40&md5=86b79ce9fd3350ff51b86519d6ba39d7
dc.relation362
dc.relationNo. 1
dc.relation355
dc.relationImmunologic Research
dc.relationVol. 65
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightsAbierto (Texto Completo)
dc.sourceinstname:Universidad del Rosario
dc.sourcereponame:Repositorio Institucional EdocUR
dc.titleCross-reactivity between annexin A2 and Beta-2-glycoprotein I in animal models of antiphospholipid syndrome
dc.typearticle


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