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Xenogeneic equine stem cells activate anti-tumor adaptive immunity in a 4T1-based intraductal mouse model for triple-negative breast cancer: proof-of-principle

Triple-negative breast cancer (TNBC) remains difficult to treat, especially due to ineffective immune responses. Current treatments mainly aim at a cytotoxic effect, whereas (stem) cell therapies are being investigated for their immune stimulatory capacities to initiate the anti-tumor immunity. Here...

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Autores principales: Steenbrugge, Jonas, Pauwelyn, Glenn, Demeyere, Kristel, Devriendt, Nausikaa, de Rooster, Hilde, Sanders, Niek N., Spaas, Jan H., Meyer, Evelyne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623058/
https://www.ncbi.nlm.nih.gov/pubmed/37928528
http://dx.doi.org/10.3389/fimmu.2023.1252374
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author Steenbrugge, Jonas
Pauwelyn, Glenn
Demeyere, Kristel
Devriendt, Nausikaa
de Rooster, Hilde
Sanders, Niek N.
Spaas, Jan H.
Meyer, Evelyne
author_facet Steenbrugge, Jonas
Pauwelyn, Glenn
Demeyere, Kristel
Devriendt, Nausikaa
de Rooster, Hilde
Sanders, Niek N.
Spaas, Jan H.
Meyer, Evelyne
author_sort Steenbrugge, Jonas
collection PubMed
description Triple-negative breast cancer (TNBC) remains difficult to treat, especially due to ineffective immune responses. Current treatments mainly aim at a cytotoxic effect, whereas (stem) cell therapies are being investigated for their immune stimulatory capacities to initiate the anti-tumor immunity. Here, a thoroughly characterized, homogenous and non-tumorigenic mixture of equine mesenchymal stem cells (eMSCs) harvested from horse peripheral blood as innovative xenogeneic immunomodulators were tested in a 4T1-based intraductal mouse model for TNBC. The eMSCs significantly reduced 4T1 progression upon systemic injection, with induction of inflammatory mediators and T-cell influx in primary tumors, already after a single dose. These xenogeneic anti-cancer effects were not restricted to MSCs as systemic treatment with alternative equine epithelial stem cells (eEpSCs) mimicked the reported disease reduction. Mechanistically, effective eMSC treatment did not rely on the spleen as systemic entrapment site, whereas CD4(+) and CD8α(+) T-cell infiltration and activation were critical. These results show that eMSCs and potentially also other equine stem cell types can be a valuable TNBC treatment strategy for further (pre)clinical evaluation.
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spelling pubmed-106230582023-11-04 Xenogeneic equine stem cells activate anti-tumor adaptive immunity in a 4T1-based intraductal mouse model for triple-negative breast cancer: proof-of-principle Steenbrugge, Jonas Pauwelyn, Glenn Demeyere, Kristel Devriendt, Nausikaa de Rooster, Hilde Sanders, Niek N. Spaas, Jan H. Meyer, Evelyne Front Immunol Immunology Triple-negative breast cancer (TNBC) remains difficult to treat, especially due to ineffective immune responses. Current treatments mainly aim at a cytotoxic effect, whereas (stem) cell therapies are being investigated for their immune stimulatory capacities to initiate the anti-tumor immunity. Here, a thoroughly characterized, homogenous and non-tumorigenic mixture of equine mesenchymal stem cells (eMSCs) harvested from horse peripheral blood as innovative xenogeneic immunomodulators were tested in a 4T1-based intraductal mouse model for TNBC. The eMSCs significantly reduced 4T1 progression upon systemic injection, with induction of inflammatory mediators and T-cell influx in primary tumors, already after a single dose. These xenogeneic anti-cancer effects were not restricted to MSCs as systemic treatment with alternative equine epithelial stem cells (eEpSCs) mimicked the reported disease reduction. Mechanistically, effective eMSC treatment did not rely on the spleen as systemic entrapment site, whereas CD4(+) and CD8α(+) T-cell infiltration and activation were critical. These results show that eMSCs and potentially also other equine stem cell types can be a valuable TNBC treatment strategy for further (pre)clinical evaluation. Frontiers Media S.A. 2023-10-20 /pmc/articles/PMC10623058/ /pubmed/37928528 http://dx.doi.org/10.3389/fimmu.2023.1252374 Text en Copyright © 2023 Steenbrugge, Pauwelyn, Demeyere, Devriendt, de Rooster, Sanders, Spaas and Meyer 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
Steenbrugge, Jonas
Pauwelyn, Glenn
Demeyere, Kristel
Devriendt, Nausikaa
de Rooster, Hilde
Sanders, Niek N.
Spaas, Jan H.
Meyer, Evelyne
Xenogeneic equine stem cells activate anti-tumor adaptive immunity in a 4T1-based intraductal mouse model for triple-negative breast cancer: proof-of-principle
title Xenogeneic equine stem cells activate anti-tumor adaptive immunity in a 4T1-based intraductal mouse model for triple-negative breast cancer: proof-of-principle
title_full Xenogeneic equine stem cells activate anti-tumor adaptive immunity in a 4T1-based intraductal mouse model for triple-negative breast cancer: proof-of-principle
title_fullStr Xenogeneic equine stem cells activate anti-tumor adaptive immunity in a 4T1-based intraductal mouse model for triple-negative breast cancer: proof-of-principle
title_full_unstemmed Xenogeneic equine stem cells activate anti-tumor adaptive immunity in a 4T1-based intraductal mouse model for triple-negative breast cancer: proof-of-principle
title_short Xenogeneic equine stem cells activate anti-tumor adaptive immunity in a 4T1-based intraductal mouse model for triple-negative breast cancer: proof-of-principle
title_sort xenogeneic equine stem cells activate anti-tumor adaptive immunity in a 4t1-based intraductal mouse model for triple-negative breast cancer: proof-of-principle
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623058/
https://www.ncbi.nlm.nih.gov/pubmed/37928528
http://dx.doi.org/10.3389/fimmu.2023.1252374
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