Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-7390
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dc.contributor.authorEbert, Stefan-
dc.contributor.authorBecker, Marc-
dc.contributor.authorLemmermann, Niels-
dc.contributor.authorBüttner, Julia K.-
dc.contributor.authorMichel, Anastasija-
dc.contributor.authorTaube, Christian-
dc.contributor.authorPodlech, Jürgen-
dc.contributor.authorBöhm, Verena-
dc.contributor.authorFreitag, Kirsten-
dc.contributor.authorThomas, Doris-
dc.contributor.authorHoltappels, Rafaela-
dc.contributor.authorReddehase, Matthias J.-
dc.contributor.authorStassen, Michael-
dc.date.accessioned2022-07-13T09:19:05Z-
dc.date.available2022-07-13T09:19:05Z-
dc.date.issued2014
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/7404-
dc.description.abstractThe lungs are a noted predilection site of acute, latent, and reactivated cytomegalovirus (CMV) infections. Interstitial pneumonia is the most dreaded manifestation of CMV disease in the immunocompromised host, whereas in the immunocompetent host lung-infiltrating CD8 T cells confine the infection in nodular inflammatory foci and prevent viral pathology. By using murine CMV infection as a model, we provide evidence for a critical role of mast cells (MC) in the recruitment of protective CD8 T cells to the lungs. Systemic infection triggered degranulation selectively in infected MC. The viral activation of MC was associated with a wave of CC chemokine ligand 5 (CCL5) in the serum of C57BL/6 mice that was MC-derived as verified by infection of MC-deficient Kit(W-sh/W-sh) "sash" mutants. In these mutants, CD8 T cells were recruited less efficiently to the lungs, correlating with enhanced viral replication and delayed virus clearance. A causative role for MC was verified by MC reconstitution of "sash" mice restoring both, efficient CD8 T-cell recruitment and infection control. These results reveal a novel crosstalk axis between innate and adaptive immune defense against CMV, and identify MC as a hitherto unconsidered player in the immune surveillance at a relevant site of CMV disease.en_GB
dc.description.sponsorshipDFG, Open Access-Publizieren Universität Mainz / Universitätsmedizinde
dc.language.isoengde
dc.rightsCC BY*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleMast cells expedite control of pulmonary murine cytomegalovirus infection by enhancing the recruitment of protective CD8 T cells to the lungsen_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-7390-
jgu.type.dinitypearticleen_GB
jgu.type.versionPublished versionde
jgu.type.resourceTextde
jgu.organisation.departmentFB 04 Medizinde
jgu.organisation.number2700-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titlePLoS pathogensde
jgu.journal.volume10de
jgu.journal.issue4de
jgu.pages.alternativee1004100de
jgu.publisher.year2014-
jgu.publisher.namePLoSde
jgu.publisher.placeLawrence, Kan.de
jgu.publisher.urihttp://dx.doi.org/10.1371/journal.ppat.1004100de
jgu.publisher.issn1553-7374de
jgu.publisher.issn1553-7366de
jgu.organisation.placeMainz-
jgu.identifier.pmid24763809
jgu.subject.ddccode610de
opus.date.modified2018-08-08T09:08:31Z
opus.subject.dfgcode00-000
opus.organisation.stringFB 04: Medizin: Institut für Virologiede_DE
opus.organisation.stringFB 04: Medizin: Institut für Immunologiede_DE
opus.identifier.opusid27385
opus.importsourcepubmed
opus.institute.number0409
opus.institute.number0412
opus.metadataonlyfalse
opus.type.contenttypeKeinede_DE
opus.type.contenttypeNoneen_EN
opus.affiliatedBecker, Marc
opus.affiliatedLemmermann, Niels
opus.affiliatedPodlech, Jürgen
opus.affiliatedHoltappels, Rafaela
opus.affiliatedReddehase, Matthias J.
opus.affiliatedStassen, Michael
jgu.publisher.doi10.1371/journal.ppat.1004100de
jgu.organisation.rorhttps://ror.org/023b0x485-
Appears in collections:DFG-OA-Publizieren (2012 - 2017)

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