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A novel lipidic peptide with potential to promote balanced effector-regulatory T cell responses
T cell-dendritic cell (DC) interactions contribute to reciprocal stimulation leading to DC maturation that results in production of interleukin-12 (IL-12) and interferon-gamma (IFN-γ). Both cytokines have been implicated in autoimmune diseases while being necessary for effective immune responses aga...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249808/ https://www.ncbi.nlm.nih.gov/pubmed/35778468 http://dx.doi.org/10.1038/s41598-022-15455-5 |
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author | Agrez, Michael Rzepecka, Justyna Turner, Darryl Knox, Gavin Chandler, Christopher Howard, Christopher B. Fletcher, Nicholas Thurecht, Kristofer Parker, Stephen Gooding, Hayley Gallagher, Laura |
author_facet | Agrez, Michael Rzepecka, Justyna Turner, Darryl Knox, Gavin Chandler, Christopher Howard, Christopher B. Fletcher, Nicholas Thurecht, Kristofer Parker, Stephen Gooding, Hayley Gallagher, Laura |
author_sort | Agrez, Michael |
collection | PubMed |
description | T cell-dendritic cell (DC) interactions contribute to reciprocal stimulation leading to DC maturation that results in production of interleukin-12 (IL-12) and interferon-gamma (IFN-γ). Both cytokines have been implicated in autoimmune diseases while being necessary for effective immune responses against foreign antigens. We describe a lipidic peptide, designated IK14004, that modifies crosstalk between T cells and DCs resulting in suppression of IL-12p40/IFN-γ production. T cell production of interleukin-2 (IL-2) and IFN-γ is uncoupled and IL-12p70 production is enhanced. IK14004 induces expression of activating co-receptors in CD8+ T cells and increases the proportion of Foxp3-expressing CD4+ T regulatory cells. The potential for IK14004 to impact on signalling pathways required to achieve a balanced immune response upon stimulation of DCs and T cells is highlighted. This novel compound provides an opportunity to gain further insights into the complexity of T cell-DC interactions relevant to autoimmunity associated with malignancies and may have therapeutic benefit. |
format | Online Article Text |
id | pubmed-9249808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-92498082022-07-03 A novel lipidic peptide with potential to promote balanced effector-regulatory T cell responses Agrez, Michael Rzepecka, Justyna Turner, Darryl Knox, Gavin Chandler, Christopher Howard, Christopher B. Fletcher, Nicholas Thurecht, Kristofer Parker, Stephen Gooding, Hayley Gallagher, Laura Sci Rep Article T cell-dendritic cell (DC) interactions contribute to reciprocal stimulation leading to DC maturation that results in production of interleukin-12 (IL-12) and interferon-gamma (IFN-γ). Both cytokines have been implicated in autoimmune diseases while being necessary for effective immune responses against foreign antigens. We describe a lipidic peptide, designated IK14004, that modifies crosstalk between T cells and DCs resulting in suppression of IL-12p40/IFN-γ production. T cell production of interleukin-2 (IL-2) and IFN-γ is uncoupled and IL-12p70 production is enhanced. IK14004 induces expression of activating co-receptors in CD8+ T cells and increases the proportion of Foxp3-expressing CD4+ T regulatory cells. The potential for IK14004 to impact on signalling pathways required to achieve a balanced immune response upon stimulation of DCs and T cells is highlighted. This novel compound provides an opportunity to gain further insights into the complexity of T cell-DC interactions relevant to autoimmunity associated with malignancies and may have therapeutic benefit. Nature Publishing Group UK 2022-07-01 /pmc/articles/PMC9249808/ /pubmed/35778468 http://dx.doi.org/10.1038/s41598-022-15455-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Agrez, Michael Rzepecka, Justyna Turner, Darryl Knox, Gavin Chandler, Christopher Howard, Christopher B. Fletcher, Nicholas Thurecht, Kristofer Parker, Stephen Gooding, Hayley Gallagher, Laura A novel lipidic peptide with potential to promote balanced effector-regulatory T cell responses |
title | A novel lipidic peptide with potential to promote balanced effector-regulatory T cell responses |
title_full | A novel lipidic peptide with potential to promote balanced effector-regulatory T cell responses |
title_fullStr | A novel lipidic peptide with potential to promote balanced effector-regulatory T cell responses |
title_full_unstemmed | A novel lipidic peptide with potential to promote balanced effector-regulatory T cell responses |
title_short | A novel lipidic peptide with potential to promote balanced effector-regulatory T cell responses |
title_sort | novel lipidic peptide with potential to promote balanced effector-regulatory t cell responses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249808/ https://www.ncbi.nlm.nih.gov/pubmed/35778468 http://dx.doi.org/10.1038/s41598-022-15455-5 |
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