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dc.contributor.authorZietara, Natalia
dc.contributor.authorŁyszkiewicz, Marcin
dc.contributor.authorPuchałka, Jacek
dc.contributor.authorPei, Gang
dc.contributor.authorGutierrez, Maximiliano Gabriel
dc.contributor.authorLienenklaus, Stefan
dc.contributor.authorHobeika, Elias
dc.contributor.authorReth, Michael
dc.contributor.authorMartins dos Santos, Vitor A P
dc.contributor.authorKrueger, Andreas
dc.contributor.authorWeiss, Siegfried
dc.date.accessioned2013-05-30T09:25:25Z
dc.date.available2013-05-30T09:25:25Z
dc.date.issued2013-02-05
dc.identifier.citationImmunoglobulins drive terminal maturation of splenic dendritic cells. 2013, 110 (6):2282-7 Proc. Natl. Acad. Sci. U.S.A.en_GB
dc.identifier.issn1091-6490
dc.identifier.pmid23345431
dc.identifier.doi10.1073/pnas.1210654110
dc.identifier.urihttp://hdl.handle.net/10033/293025
dc.description.abstractNature and physiological status of antigen-presenting cells, such as dendritic cells DCs, are decisive for the immune reactions elicited. Multiple factors and cell interactions have been described that affect maturation of DCs. Here, we show that DCs arising in the absence of immunoglobulins (Ig) in vivo are impaired in cross-presentation of soluble antigen. This deficiency was due to aberrant cellular targeting of antigen to lysosomes and its rapid degradation. Function of DCs could be restored by transfer of Ig irrespective of antigen specificity and isotype. Modulation of cross-presentation by Ig was inhibited by coapplication of mannan and, thus, likely to be mediated by C-type lectin receptors. This unexpected dependency of splenic DCs on Ig to cross-present antigen provides insights into the interplay between cellular and humoral immunity and the immunomodulatory capacity of Ig.
dc.language.isoenen
dc.rightsArchived with thanks to Proceedings of the National Academy of Sciences of the United States of Americaen_GB
dc.subject.meshAnimalsen_GB
dc.subject.meshB-Lymphocytesen_GB
dc.subject.meshCell Differentiationen_GB
dc.subject.meshCross-Primingen_GB
dc.subject.meshDendritic Cellsen_GB
dc.subject.meshFemaleen_GB
dc.subject.meshImmunoglobulinsen_GB
dc.subject.meshLectins, C-Typeen_GB
dc.subject.meshLymphopeniaen_GB
dc.subject.meshMiceen_GB
dc.subject.meshMice, Inbred C57BLen_GB
dc.subject.meshMice, Knockouten_GB
dc.subject.meshSpleenen_GB
dc.subject.meshT-Lymphocytesen_GB
dc.titleImmunoglobulins drive terminal maturation of splenic dendritic cells.en
dc.typeArticleen
dc.contributor.departmentDepartment of Molecular Immunology, Helmholtz Centre for Infection Research, 38124 Braunschweig, Germany. zietara.natalia@mh-hannover.deen_GB
dc.identifier.journalProceedings of the National Academy of Sciences of the United States of Americaen_GB
refterms.dateFOA2018-06-12T21:56:43Z
html.description.abstractNature and physiological status of antigen-presenting cells, such as dendritic cells DCs, are decisive for the immune reactions elicited. Multiple factors and cell interactions have been described that affect maturation of DCs. Here, we show that DCs arising in the absence of immunoglobulins (Ig) in vivo are impaired in cross-presentation of soluble antigen. This deficiency was due to aberrant cellular targeting of antigen to lysosomes and its rapid degradation. Function of DCs could be restored by transfer of Ig irrespective of antigen specificity and isotype. Modulation of cross-presentation by Ig was inhibited by coapplication of mannan and, thus, likely to be mediated by C-type lectin receptors. This unexpected dependency of splenic DCs on Ig to cross-present antigen provides insights into the interplay between cellular and humoral immunity and the immunomodulatory capacity of Ig.


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