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dc.contributor.authorKnuschke, Torben
dc.contributor.authorRotan, Olga
dc.contributor.authorBayer, Wibke
dc.contributor.authorSokolova, Viktoriya
dc.contributor.authorHansen, Wiebke
dc.contributor.authorSparwasser, Tim
dc.contributor.authorDittmer, Ulf
dc.contributor.authorEpple, Matthias
dc.contributor.authorBuer, Jan
dc.contributor.authorWestendorf, Astrid M
dc.date.accessioned2016-05-17T14:42:26Zen
dc.date.available2016-05-17T14:42:26Zen
dc.date.issued2016en
dc.identifier.citationCombination of nanoparticle-based therapeutic vaccination and transient ablation of regulatory T cells enhances anti-viral immunity during chronic retroviral infection. 2016, 13:24 Retrovirologyen
dc.identifier.issn1742-4690en
dc.identifier.pmid27076190en
dc.identifier.doi10.1186/s12977-016-0258-9en
dc.identifier.urihttp://hdl.handle.net/10033/609566en
dc.description.abstractRegulatory T cells (Tregs) have been shown to limit anti-viral immunity during chronic retroviral infection and to restrict vaccine-induced T cell responses. The objective of the study was to assess whether a combinational therapy of nanoparticle-based therapeutic vaccination and concomitant transient ablation of Tregs augments anti-viral immunity and improves virus control in chronically retrovirus-infected mice. Therefore, chronically Friend retrovirus (FV)-infected mice were immunized with calcium phosphate (CaP) nanoparticles functionalized with TLR9 ligand CpG and CD8(+) or CD4(+) T cell epitope peptides (GagL85-93 or Env gp70123-141) of FV. In addition, Tregs were ablated during the immunization process. Reactivation of CD4(+) and CD8(+) effector T cells was analysed and the viral loads were determined.
dc.language.isoenen
dc.titleCombination of nanoparticle-based therapeutic vaccination and transient ablation of regulatory T cells enhances anti-viral immunity during chronic retroviral infection.en
dc.typeArticleen
dc.contributor.departmentTWINCORE, Centre for Experimental and Clinical Medicine, 30625 Hannover, Germany.en
dc.identifier.journalRetrovirologyen
refterms.dateFOA2018-06-13T02:25:28Z
html.description.abstractRegulatory T cells (Tregs) have been shown to limit anti-viral immunity during chronic retroviral infection and to restrict vaccine-induced T cell responses. The objective of the study was to assess whether a combinational therapy of nanoparticle-based therapeutic vaccination and concomitant transient ablation of Tregs augments anti-viral immunity and improves virus control in chronically retrovirus-infected mice. Therefore, chronically Friend retrovirus (FV)-infected mice were immunized with calcium phosphate (CaP) nanoparticles functionalized with TLR9 ligand CpG and CD8(+) or CD4(+) T cell epitope peptides (GagL85-93 or Env gp70123-141) of FV. In addition, Tregs were ablated during the immunization process. Reactivation of CD4(+) and CD8(+) effector T cells was analysed and the viral loads were determined.


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