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Monitoring islet specific immune responses in type 1 diabetes clinical immunotherapy trials
The number of immunotherapeutic clinical trials in type 1 diabetes currently being conducted is expanding, and thus there is a need for robust immune-monitoring assays which are capable of detecting and characterizing islet specific immune responses in peripheral blood. Islet- specific T cells can s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240960/ https://www.ncbi.nlm.nih.gov/pubmed/37283770 http://dx.doi.org/10.3389/fimmu.2023.1183909 |
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author | Arif, Sefina Domingo-Vila, Clara Pollock, Emily Christakou, Eleni Williams, Evangelia Tree, Timothy I. M. |
author_facet | Arif, Sefina Domingo-Vila, Clara Pollock, Emily Christakou, Eleni Williams, Evangelia Tree, Timothy I. M. |
author_sort | Arif, Sefina |
collection | PubMed |
description | The number of immunotherapeutic clinical trials in type 1 diabetes currently being conducted is expanding, and thus there is a need for robust immune-monitoring assays which are capable of detecting and characterizing islet specific immune responses in peripheral blood. Islet- specific T cells can serve as biomarkers and as such can guide drug selection, dosing regimens and immunological efficacy. Furthermore, these biomarkers can be utilized in patient stratification which can then benchmark suitability for participation in future clinical trials. This review focusses on the commonly used immune-monitoring techniques including multimer and antigen induced marker assays and the potential to combine these with single cell transcriptional profiling which may provide a greater understanding of the mechanisms underlying immuno-intervention. Although challenges remain around some key areas such as the need for harmonizing assays, technological advances mean that multiparametric information derived from a single sample can be used in coordinated efforts to harmonize biomarker discovery and validation. Moreover, the technologies discussed here have the potential to provide a unique insight on the effect of therapies on key players in the pathogenesis of T1D that cannot be obtained using antigen agnostic approaches. |
format | Online Article Text |
id | pubmed-10240960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102409602023-06-06 Monitoring islet specific immune responses in type 1 diabetes clinical immunotherapy trials Arif, Sefina Domingo-Vila, Clara Pollock, Emily Christakou, Eleni Williams, Evangelia Tree, Timothy I. M. Front Immunol Immunology The number of immunotherapeutic clinical trials in type 1 diabetes currently being conducted is expanding, and thus there is a need for robust immune-monitoring assays which are capable of detecting and characterizing islet specific immune responses in peripheral blood. Islet- specific T cells can serve as biomarkers and as such can guide drug selection, dosing regimens and immunological efficacy. Furthermore, these biomarkers can be utilized in patient stratification which can then benchmark suitability for participation in future clinical trials. This review focusses on the commonly used immune-monitoring techniques including multimer and antigen induced marker assays and the potential to combine these with single cell transcriptional profiling which may provide a greater understanding of the mechanisms underlying immuno-intervention. Although challenges remain around some key areas such as the need for harmonizing assays, technological advances mean that multiparametric information derived from a single sample can be used in coordinated efforts to harmonize biomarker discovery and validation. Moreover, the technologies discussed here have the potential to provide a unique insight on the effect of therapies on key players in the pathogenesis of T1D that cannot be obtained using antigen agnostic approaches. Frontiers Media S.A. 2023-05-22 /pmc/articles/PMC10240960/ /pubmed/37283770 http://dx.doi.org/10.3389/fimmu.2023.1183909 Text en Copyright © 2023 Arif, Domingo-Vila, Pollock, Christakou, Williams and Tree 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 Arif, Sefina Domingo-Vila, Clara Pollock, Emily Christakou, Eleni Williams, Evangelia Tree, Timothy I. M. Monitoring islet specific immune responses in type 1 diabetes clinical immunotherapy trials |
title | Monitoring islet specific immune responses in type 1 diabetes clinical immunotherapy trials |
title_full | Monitoring islet specific immune responses in type 1 diabetes clinical immunotherapy trials |
title_fullStr | Monitoring islet specific immune responses in type 1 diabetes clinical immunotherapy trials |
title_full_unstemmed | Monitoring islet specific immune responses in type 1 diabetes clinical immunotherapy trials |
title_short | Monitoring islet specific immune responses in type 1 diabetes clinical immunotherapy trials |
title_sort | monitoring islet specific immune responses in type 1 diabetes clinical immunotherapy trials |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240960/ https://www.ncbi.nlm.nih.gov/pubmed/37283770 http://dx.doi.org/10.3389/fimmu.2023.1183909 |
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