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Trained Immunity as an Adaptive Branch of Innate Immunity

The concept of trained immunity has become one of the most interesting and potentially commercially and clinically relevant ideas of current immunology. Trained immunity is realized by the epigenetic reprogramming of non-immunocompetent cells, primarily monocytes/macrophages and natural killer (NK)...

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Detalles Bibliográficos
Autores principales: Vetvicka, Vaclav, Sima, Petr, Vannucci, Luca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8508929/
https://www.ncbi.nlm.nih.gov/pubmed/34639025
http://dx.doi.org/10.3390/ijms221910684
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author Vetvicka, Vaclav
Sima, Petr
Vannucci, Luca
author_facet Vetvicka, Vaclav
Sima, Petr
Vannucci, Luca
author_sort Vetvicka, Vaclav
collection PubMed
description The concept of trained immunity has become one of the most interesting and potentially commercially and clinically relevant ideas of current immunology. Trained immunity is realized by the epigenetic reprogramming of non-immunocompetent cells, primarily monocytes/macrophages and natural killer (NK) cells, and is less specific than adaptive immunity; therefore, it may cross-protect against other infectious agents. It remains possible, however, that some of the observed changes are simply caused by increased levels of immune reactions resulting from supplementation with immunomodulators, such as glucan. In addition, the question of whether we can talk about trained immunity in cells with a life span of only few days is still unresolved.
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spelling pubmed-85089292021-10-13 Trained Immunity as an Adaptive Branch of Innate Immunity Vetvicka, Vaclav Sima, Petr Vannucci, Luca Int J Mol Sci Review The concept of trained immunity has become one of the most interesting and potentially commercially and clinically relevant ideas of current immunology. Trained immunity is realized by the epigenetic reprogramming of non-immunocompetent cells, primarily monocytes/macrophages and natural killer (NK) cells, and is less specific than adaptive immunity; therefore, it may cross-protect against other infectious agents. It remains possible, however, that some of the observed changes are simply caused by increased levels of immune reactions resulting from supplementation with immunomodulators, such as glucan. In addition, the question of whether we can talk about trained immunity in cells with a life span of only few days is still unresolved. MDPI 2021-10-01 /pmc/articles/PMC8508929/ /pubmed/34639025 http://dx.doi.org/10.3390/ijms221910684 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Vetvicka, Vaclav
Sima, Petr
Vannucci, Luca
Trained Immunity as an Adaptive Branch of Innate Immunity
title Trained Immunity as an Adaptive Branch of Innate Immunity
title_full Trained Immunity as an Adaptive Branch of Innate Immunity
title_fullStr Trained Immunity as an Adaptive Branch of Innate Immunity
title_full_unstemmed Trained Immunity as an Adaptive Branch of Innate Immunity
title_short Trained Immunity as an Adaptive Branch of Innate Immunity
title_sort trained immunity as an adaptive branch of innate immunity
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8508929/
https://www.ncbi.nlm.nih.gov/pubmed/34639025
http://dx.doi.org/10.3390/ijms221910684
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