Storage-induced changes in erythrocyte membrane proteins promote recognition by autoantibodies.

Physiological erythrocyte removal is associated with a selective increase in expression of neoantigens on erythrocytes and their vesicles, and subsequent autologous antibody binding and phagocytosis. Chronic erythrocyte transfusion often leads to immunization and the formation of alloantibodies and...

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Main Authors: Sip Dinkla, Věra M J Novotný, Irma Joosten, Giel J C G M Bosman
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3411782?pdf=render
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author Sip Dinkla
Věra M J Novotný
Irma Joosten
Giel J C G M Bosman
author_facet Sip Dinkla
Věra M J Novotný
Irma Joosten
Giel J C G M Bosman
author_sort Sip Dinkla
collection DOAJ
description Physiological erythrocyte removal is associated with a selective increase in expression of neoantigens on erythrocytes and their vesicles, and subsequent autologous antibody binding and phagocytosis. Chronic erythrocyte transfusion often leads to immunization and the formation of alloantibodies and autoantibodies. We investigated whether erythrocyte storage leads to the increased expression of non-physiological antigens. Immunoprecipitations were performed with erythrocytes and vesicles from blood bank erythrocyte concentrates of increasing storage periods, using patient plasma containing erythrocyte autoantibodies. Immunoprecipitate composition was identified using proteomics. Patient plasma antibody binding increased with erythrocyte storage time, while the opposite was observed for healthy volunteer plasma, showing that pathology-associated antigenicity changes during erythrocyte storage. Several membrane proteins were identified as candidate antigens. The protein complexes that were precipitated by the patient antibodies in erythrocytes were different from the ones in the vesicles formed during erythrocyte storage, indicating that the storage-associated vesicles have a different immunization potential. Soluble immune mediators including complement factors were present in the patient plasma immunoprecipitates, but not in the allogeneic control immunoprecipitates. The results support the theory that disturbed erythrocyte aging during storage of erythrocyte concentrates contributes to transfusion-induced alloantibody and autoantibody formation.
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spelling doaj.art-70947860a11a4e29a0187926e8fe68142022-12-22T02:51:15ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0178e4225010.1371/journal.pone.0042250Storage-induced changes in erythrocyte membrane proteins promote recognition by autoantibodies.Sip DinklaVěra M J NovotnýIrma JoostenGiel J C G M BosmanPhysiological erythrocyte removal is associated with a selective increase in expression of neoantigens on erythrocytes and their vesicles, and subsequent autologous antibody binding and phagocytosis. Chronic erythrocyte transfusion often leads to immunization and the formation of alloantibodies and autoantibodies. We investigated whether erythrocyte storage leads to the increased expression of non-physiological antigens. Immunoprecipitations were performed with erythrocytes and vesicles from blood bank erythrocyte concentrates of increasing storage periods, using patient plasma containing erythrocyte autoantibodies. Immunoprecipitate composition was identified using proteomics. Patient plasma antibody binding increased with erythrocyte storage time, while the opposite was observed for healthy volunteer plasma, showing that pathology-associated antigenicity changes during erythrocyte storage. Several membrane proteins were identified as candidate antigens. The protein complexes that were precipitated by the patient antibodies in erythrocytes were different from the ones in the vesicles formed during erythrocyte storage, indicating that the storage-associated vesicles have a different immunization potential. Soluble immune mediators including complement factors were present in the patient plasma immunoprecipitates, but not in the allogeneic control immunoprecipitates. The results support the theory that disturbed erythrocyte aging during storage of erythrocyte concentrates contributes to transfusion-induced alloantibody and autoantibody formation.http://europepmc.org/articles/PMC3411782?pdf=render
spellingShingle Sip Dinkla
Věra M J Novotný
Irma Joosten
Giel J C G M Bosman
Storage-induced changes in erythrocyte membrane proteins promote recognition by autoantibodies.
PLoS ONE
title Storage-induced changes in erythrocyte membrane proteins promote recognition by autoantibodies.
title_full Storage-induced changes in erythrocyte membrane proteins promote recognition by autoantibodies.
title_fullStr Storage-induced changes in erythrocyte membrane proteins promote recognition by autoantibodies.
title_full_unstemmed Storage-induced changes in erythrocyte membrane proteins promote recognition by autoantibodies.
title_short Storage-induced changes in erythrocyte membrane proteins promote recognition by autoantibodies.
title_sort storage induced changes in erythrocyte membrane proteins promote recognition by autoantibodies
url http://europepmc.org/articles/PMC3411782?pdf=render
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AT irmajoosten storageinducedchangesinerythrocytemembraneproteinspromoterecognitionbyautoantibodies
AT gieljcgmbosman storageinducedchangesinerythrocytemembraneproteinspromoterecognitionbyautoantibodies