Type 1 diabetes vaccine candidates promote human Foxp3+Treg induction in humanized mice
Type 1 diabetes is associated with the loss of self-tolerance to the insulin-producing β-cells in the pancreas. Here the authors show that vaccination with insulin mimetopes can induce human insulin-specific regulatory T cells to mediate tolerance in a humanized mouse model.
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2016-03-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/ncomms10991 |
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doaj-384e9f53afaf4353a75ebc119a70470f2021-05-11T10:50:35ZengNature Publishing GroupNature Communications2041-17232016-03-017111810.1038/ncomms10991Type 1 diabetes vaccine candidates promote human Foxp3+Treg induction in humanized miceIsabelle Serr0Rainer W. Fürst1Peter Achenbach2Martin G. Scherm3Füsun Gökmen4Florian Haupt5Eva-Maria Sedlmeier6Annette Knopff7Leonard Shultz8Richard A. Willis9Anette-Gabriele Ziegler10Carolin Daniel11Institute for Diabetes Research, Independent Young Investigator Group Immune Tolerance in Type 1 Diabetes, Helmholtz Diabetes Center at Helmholtz Zentrum MünchenDeutsches Zentrum für Diabetesforschung (DZD)Deutsches Zentrum für Diabetesforschung (DZD)Institute for Diabetes Research, Independent Young Investigator Group Immune Tolerance in Type 1 Diabetes, Helmholtz Diabetes Center at Helmholtz Zentrum MünchenInstitute for Diabetes Research, Independent Young Investigator Group Immune Tolerance in Type 1 Diabetes, Helmholtz Diabetes Center at Helmholtz Zentrum MünchenDeutsches Zentrum für Diabetesforschung (DZD)Deutsches Zentrum für Diabetesforschung (DZD)Deutsches Zentrum für Diabetesforschung (DZD)The Jackson LaboratoryEmory Vaccine Center, NIH Tetramer Core FacilityDeutsches Zentrum für Diabetesforschung (DZD)Institute for Diabetes Research, Independent Young Investigator Group Immune Tolerance in Type 1 Diabetes, Helmholtz Diabetes Center at Helmholtz Zentrum MünchenType 1 diabetes is associated with the loss of self-tolerance to the insulin-producing β-cells in the pancreas. Here the authors show that vaccination with insulin mimetopes can induce human insulin-specific regulatory T cells to mediate tolerance in a humanized mouse model.https://doi.org/10.1038/ncomms10991 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Isabelle Serr Rainer W. Fürst Peter Achenbach Martin G. Scherm Füsun Gökmen Florian Haupt Eva-Maria Sedlmeier Annette Knopff Leonard Shultz Richard A. Willis Anette-Gabriele Ziegler Carolin Daniel |
spellingShingle |
Isabelle Serr Rainer W. Fürst Peter Achenbach Martin G. Scherm Füsun Gökmen Florian Haupt Eva-Maria Sedlmeier Annette Knopff Leonard Shultz Richard A. Willis Anette-Gabriele Ziegler Carolin Daniel Type 1 diabetes vaccine candidates promote human Foxp3+Treg induction in humanized mice Nature Communications |
author_facet |
Isabelle Serr Rainer W. Fürst Peter Achenbach Martin G. Scherm Füsun Gökmen Florian Haupt Eva-Maria Sedlmeier Annette Knopff Leonard Shultz Richard A. Willis Anette-Gabriele Ziegler Carolin Daniel |
author_sort |
Isabelle Serr |
title |
Type 1 diabetes vaccine candidates promote human Foxp3+Treg induction in humanized mice |
title_short |
Type 1 diabetes vaccine candidates promote human Foxp3+Treg induction in humanized mice |
title_full |
Type 1 diabetes vaccine candidates promote human Foxp3+Treg induction in humanized mice |
title_fullStr |
Type 1 diabetes vaccine candidates promote human Foxp3+Treg induction in humanized mice |
title_full_unstemmed |
Type 1 diabetes vaccine candidates promote human Foxp3+Treg induction in humanized mice |
title_sort |
type 1 diabetes vaccine candidates promote human foxp3+treg induction in humanized mice |
publisher |
Nature Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2016-03-01 |
description |
Type 1 diabetes is associated with the loss of self-tolerance to the insulin-producing β-cells in the pancreas. Here the authors show that vaccination with insulin mimetopes can induce human insulin-specific regulatory T cells to mediate tolerance in a humanized mouse model. |
url |
https://doi.org/10.1038/ncomms10991 |
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