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Nanodrugs Targeting T Cells in Tumor Therapy

In contrast to conventional anti-tumor agents, nano-carriers allow co-delivery of distinct drugs in a cell type-specific manner. So far, many nanodrug-based immunotherapeutic approaches aim to target and kill tumor cells directly or to address antigen presenting cells (APC) like dendritic cells (DC)...

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Autores principales: Haist, Maximilian, Mailänder, Volker, Bros, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9174908/
https://www.ncbi.nlm.nih.gov/pubmed/35693776
http://dx.doi.org/10.3389/fimmu.2022.912594
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author Haist, Maximilian
Mailänder, Volker
Bros, Matthias
author_facet Haist, Maximilian
Mailänder, Volker
Bros, Matthias
author_sort Haist, Maximilian
collection PubMed
description In contrast to conventional anti-tumor agents, nano-carriers allow co-delivery of distinct drugs in a cell type-specific manner. So far, many nanodrug-based immunotherapeutic approaches aim to target and kill tumor cells directly or to address antigen presenting cells (APC) like dendritic cells (DC) in order to elicit tumor antigen-specific T cell responses. Regulatory T cells (Treg) constitute a major obstacle in tumor therapy by inducing a pro-tolerogenic state in APC and inhibiting T cell activation and T effector cell activity. This review aims to summarize nanodrug-based strategies that aim to address and reprogram Treg to overcome their immunomodulatory activity and to revert the exhaustive state of T effector cells. Further, we will also discuss nano-carrier-based approaches to introduce tumor antigen-specific chimeric antigen receptors (CAR) into T cells for CAR-T cell therapy which constitutes a complementary approach to DC-focused vaccination.
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spelling pubmed-91749082022-06-09 Nanodrugs Targeting T Cells in Tumor Therapy Haist, Maximilian Mailänder, Volker Bros, Matthias Front Immunol Immunology In contrast to conventional anti-tumor agents, nano-carriers allow co-delivery of distinct drugs in a cell type-specific manner. So far, many nanodrug-based immunotherapeutic approaches aim to target and kill tumor cells directly or to address antigen presenting cells (APC) like dendritic cells (DC) in order to elicit tumor antigen-specific T cell responses. Regulatory T cells (Treg) constitute a major obstacle in tumor therapy by inducing a pro-tolerogenic state in APC and inhibiting T cell activation and T effector cell activity. This review aims to summarize nanodrug-based strategies that aim to address and reprogram Treg to overcome their immunomodulatory activity and to revert the exhaustive state of T effector cells. Further, we will also discuss nano-carrier-based approaches to introduce tumor antigen-specific chimeric antigen receptors (CAR) into T cells for CAR-T cell therapy which constitutes a complementary approach to DC-focused vaccination. Frontiers Media S.A. 2022-05-25 /pmc/articles/PMC9174908/ /pubmed/35693776 http://dx.doi.org/10.3389/fimmu.2022.912594 Text en Copyright © 2022 Haist, Mailänder and Bros 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
Haist, Maximilian
Mailänder, Volker
Bros, Matthias
Nanodrugs Targeting T Cells in Tumor Therapy
title Nanodrugs Targeting T Cells in Tumor Therapy
title_full Nanodrugs Targeting T Cells in Tumor Therapy
title_fullStr Nanodrugs Targeting T Cells in Tumor Therapy
title_full_unstemmed Nanodrugs Targeting T Cells in Tumor Therapy
title_short Nanodrugs Targeting T Cells in Tumor Therapy
title_sort nanodrugs targeting t cells in tumor therapy
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9174908/
https://www.ncbi.nlm.nih.gov/pubmed/35693776
http://dx.doi.org/10.3389/fimmu.2022.912594
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