Cargando…
Human amniotic fluid derived extracellular vesicles attenuate T cell immune response
INTRODUCTION: Extracellular vesicles isolated from human amniotic fluid (AF-EVs) have previously been found to modulate inflammation and macrophage infiltration in a mouse model. However, the effects of acellular amniotic fluid (acAF) or AF-EVs on the T-Cell immune response have not been explored. M...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742275/ https://www.ncbi.nlm.nih.gov/pubmed/36518766 http://dx.doi.org/10.3389/fimmu.2022.977809 |
_version_ | 1784848490826825728 |
---|---|
author | del Rivero, Tania Milberg, Julian Bennett, Cassie Mitrani, Maria Ines Bellio, Michael A. |
author_facet | del Rivero, Tania Milberg, Julian Bennett, Cassie Mitrani, Maria Ines Bellio, Michael A. |
author_sort | del Rivero, Tania |
collection | PubMed |
description | INTRODUCTION: Extracellular vesicles isolated from human amniotic fluid (AF-EVs) have previously been found to modulate inflammation and macrophage infiltration in a mouse model. However, the effects of acellular amniotic fluid (acAF) or AF-EVs on the T-Cell immune response have not been explored. METHODS: In this study, we investigated the effects of acAF and AF-EVs on the T cell immune response in an in vitro cell culture model. Peripheral Blood Mononuclear Cells (PBMCs) were stimulated with Phytohemagglutinin (PHA) to induce the immune response and were subsequently treated with either serum-free media (vehicle), acAF, or concentrated AF-EVs. RESULTS: Both acAF and AF-EV treatment suppressed PHA-induced T cell proliferation and PHA-induced T cell activation; however, treatment with concentrated AF-EVs had a greater effect. Additionally, both acAF and AF-EVs reduced PBMC pro-inflammatory cytokine release. AF-EVs were found to be taken up by both CD4+ and CD8+ effector T cell subsets. CONCLUSION: Overall, this data demonstrates that AF-EVs have a robust immunomodulatory effect on T cells and suggests AF-EVs could be used as an immunotherapeutic tool. |
format | Online Article Text |
id | pubmed-9742275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97422752022-12-13 Human amniotic fluid derived extracellular vesicles attenuate T cell immune response del Rivero, Tania Milberg, Julian Bennett, Cassie Mitrani, Maria Ines Bellio, Michael A. Front Immunol Immunology INTRODUCTION: Extracellular vesicles isolated from human amniotic fluid (AF-EVs) have previously been found to modulate inflammation and macrophage infiltration in a mouse model. However, the effects of acellular amniotic fluid (acAF) or AF-EVs on the T-Cell immune response have not been explored. METHODS: In this study, we investigated the effects of acAF and AF-EVs on the T cell immune response in an in vitro cell culture model. Peripheral Blood Mononuclear Cells (PBMCs) were stimulated with Phytohemagglutinin (PHA) to induce the immune response and were subsequently treated with either serum-free media (vehicle), acAF, or concentrated AF-EVs. RESULTS: Both acAF and AF-EV treatment suppressed PHA-induced T cell proliferation and PHA-induced T cell activation; however, treatment with concentrated AF-EVs had a greater effect. Additionally, both acAF and AF-EVs reduced PBMC pro-inflammatory cytokine release. AF-EVs were found to be taken up by both CD4+ and CD8+ effector T cell subsets. CONCLUSION: Overall, this data demonstrates that AF-EVs have a robust immunomodulatory effect on T cells and suggests AF-EVs could be used as an immunotherapeutic tool. Frontiers Media S.A. 2022-11-28 /pmc/articles/PMC9742275/ /pubmed/36518766 http://dx.doi.org/10.3389/fimmu.2022.977809 Text en Copyright © 2022 del Rivero, Milberg, Bennett, Mitrani and Bellio https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology del Rivero, Tania Milberg, Julian Bennett, Cassie Mitrani, Maria Ines Bellio, Michael A. Human amniotic fluid derived extracellular vesicles attenuate T cell immune response |
title | Human amniotic fluid derived extracellular vesicles attenuate T cell immune response |
title_full | Human amniotic fluid derived extracellular vesicles attenuate T cell immune response |
title_fullStr | Human amniotic fluid derived extracellular vesicles attenuate T cell immune response |
title_full_unstemmed | Human amniotic fluid derived extracellular vesicles attenuate T cell immune response |
title_short | Human amniotic fluid derived extracellular vesicles attenuate T cell immune response |
title_sort | human amniotic fluid derived extracellular vesicles attenuate t cell immune response |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742275/ https://www.ncbi.nlm.nih.gov/pubmed/36518766 http://dx.doi.org/10.3389/fimmu.2022.977809 |
work_keys_str_mv | AT delriverotania humanamnioticfluidderivedextracellularvesiclesattenuatetcellimmuneresponse AT milbergjulian humanamnioticfluidderivedextracellularvesiclesattenuatetcellimmuneresponse AT bennettcassie humanamnioticfluidderivedextracellularvesiclesattenuatetcellimmuneresponse AT mitranimariaines humanamnioticfluidderivedextracellularvesiclesattenuatetcellimmuneresponse AT belliomichaela humanamnioticfluidderivedextracellularvesiclesattenuatetcellimmuneresponse |