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Chronic myeloid leukemia‐derived extracellular vesicles increase Foxp3 level and suppressive activity of thymic regulatory T cells
Mechanisms driving immunosuppression in chronic myeloid leukemia are mostly unknown. We show that leukemic extracellular vesicles (EVs) target lymphocytes and amplify suppressive function of thymic regulatory T cells, by driving expression of Foxp3 transcription factor. This could facilitate expansi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187374/ https://www.ncbi.nlm.nih.gov/pubmed/31758697 http://dx.doi.org/10.1002/eji.201848051 |
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author | Swatler, Julian Dudka, Wioleta Bugajski, Lukasz Brewinska‐Olchowik, Marta Kozlowska, Ewa Piwocka, Katarzyna |
author_facet | Swatler, Julian Dudka, Wioleta Bugajski, Lukasz Brewinska‐Olchowik, Marta Kozlowska, Ewa Piwocka, Katarzyna |
author_sort | Swatler, Julian |
collection | PubMed |
description | Mechanisms driving immunosuppression in chronic myeloid leukemia are mostly unknown. We show that leukemic extracellular vesicles (EVs) target lymphocytes and amplify suppressive function of thymic regulatory T cells, by driving expression of Foxp3 transcription factor. This could facilitate expansion of leukemic cells outside the bone marrow, leading to blast crisis. [Image: see text] |
format | Online Article Text |
id | pubmed-7187374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71873742020-04-28 Chronic myeloid leukemia‐derived extracellular vesicles increase Foxp3 level and suppressive activity of thymic regulatory T cells Swatler, Julian Dudka, Wioleta Bugajski, Lukasz Brewinska‐Olchowik, Marta Kozlowska, Ewa Piwocka, Katarzyna Eur J Immunol Letter to the Editor Mechanisms driving immunosuppression in chronic myeloid leukemia are mostly unknown. We show that leukemic extracellular vesicles (EVs) target lymphocytes and amplify suppressive function of thymic regulatory T cells, by driving expression of Foxp3 transcription factor. This could facilitate expansion of leukemic cells outside the bone marrow, leading to blast crisis. [Image: see text] John Wiley and Sons Inc. 2019-12-05 2020-04 /pmc/articles/PMC7187374/ /pubmed/31758697 http://dx.doi.org/10.1002/eji.201848051 Text en © 2019 The Authors. European Journal of Immunology published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Letter to the Editor Swatler, Julian Dudka, Wioleta Bugajski, Lukasz Brewinska‐Olchowik, Marta Kozlowska, Ewa Piwocka, Katarzyna Chronic myeloid leukemia‐derived extracellular vesicles increase Foxp3 level and suppressive activity of thymic regulatory T cells |
title | Chronic myeloid leukemia‐derived extracellular vesicles increase Foxp3 level and suppressive activity of thymic regulatory T cells |
title_full | Chronic myeloid leukemia‐derived extracellular vesicles increase Foxp3 level and suppressive activity of thymic regulatory T cells |
title_fullStr | Chronic myeloid leukemia‐derived extracellular vesicles increase Foxp3 level and suppressive activity of thymic regulatory T cells |
title_full_unstemmed | Chronic myeloid leukemia‐derived extracellular vesicles increase Foxp3 level and suppressive activity of thymic regulatory T cells |
title_short | Chronic myeloid leukemia‐derived extracellular vesicles increase Foxp3 level and suppressive activity of thymic regulatory T cells |
title_sort | chronic myeloid leukemia‐derived extracellular vesicles increase foxp3 level and suppressive activity of thymic regulatory t cells |
topic | Letter to the Editor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187374/ https://www.ncbi.nlm.nih.gov/pubmed/31758697 http://dx.doi.org/10.1002/eji.201848051 |
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