Cargando…

Determining Antigen Specificity of Human Islet Infiltrating T Cells in Type 1 Diabetes

Type 1 diabetes, the immune mediated form of diabetes, represents a prototypical organ specific autoimmune disease in that insulin producing pancreatic islets are specifically targeted by T cells. The disease is now predictable in humans with the measurement of type 1 diabetes associated autoantibod...

Descripción completa

Detalles Bibliográficos
Autores principales: Nakayama, Maki, Michels, Aaron W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418007/
https://www.ncbi.nlm.nih.gov/pubmed/30906293
http://dx.doi.org/10.3389/fimmu.2019.00365
_version_ 1783403640647581696
author Nakayama, Maki
Michels, Aaron W.
author_facet Nakayama, Maki
Michels, Aaron W.
author_sort Nakayama, Maki
collection PubMed
description Type 1 diabetes, the immune mediated form of diabetes, represents a prototypical organ specific autoimmune disease in that insulin producing pancreatic islets are specifically targeted by T cells. The disease is now predictable in humans with the measurement of type 1 diabetes associated autoantibodies (islet autoantibodies) in the peripheral blood which are directed against insulin and beta cell proteins. With an increasing incidence of disease, especially in young children, large well-controlled clinical prevention trials using antigen specific immunotherapy have been completed but with limited clinical benefit. To improve outcomes, it is critical to understand the antigen and T cell receptor repertoires of those cells that infiltrate the target organ, pancreatic islets, in human type 1 diabetes. With international networks to identify organ donors with type 1 diabetes, improved immunosequencing platforms, and the ability to reconstitute T cell receptors of interest into immortalized cell lines allows antigen discovery efforts for rare tissue specific T cells. Here we review the disease pathogenesis of type 1 diabetes with a focus on human islet infiltrating T cell antigen discovery efforts, which provides necessary knowledge to define biomarkers of disease activity and improve antigen specific immunotherapy approaches for disease prevention.
format Online
Article
Text
id pubmed-6418007
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-64180072019-03-22 Determining Antigen Specificity of Human Islet Infiltrating T Cells in Type 1 Diabetes Nakayama, Maki Michels, Aaron W. Front Immunol Immunology Type 1 diabetes, the immune mediated form of diabetes, represents a prototypical organ specific autoimmune disease in that insulin producing pancreatic islets are specifically targeted by T cells. The disease is now predictable in humans with the measurement of type 1 diabetes associated autoantibodies (islet autoantibodies) in the peripheral blood which are directed against insulin and beta cell proteins. With an increasing incidence of disease, especially in young children, large well-controlled clinical prevention trials using antigen specific immunotherapy have been completed but with limited clinical benefit. To improve outcomes, it is critical to understand the antigen and T cell receptor repertoires of those cells that infiltrate the target organ, pancreatic islets, in human type 1 diabetes. With international networks to identify organ donors with type 1 diabetes, improved immunosequencing platforms, and the ability to reconstitute T cell receptors of interest into immortalized cell lines allows antigen discovery efforts for rare tissue specific T cells. Here we review the disease pathogenesis of type 1 diabetes with a focus on human islet infiltrating T cell antigen discovery efforts, which provides necessary knowledge to define biomarkers of disease activity and improve antigen specific immunotherapy approaches for disease prevention. Frontiers Media S.A. 2019-03-08 /pmc/articles/PMC6418007/ /pubmed/30906293 http://dx.doi.org/10.3389/fimmu.2019.00365 Text en Copyright © 2019 Nakayama and Michels. http://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
Nakayama, Maki
Michels, Aaron W.
Determining Antigen Specificity of Human Islet Infiltrating T Cells in Type 1 Diabetes
title Determining Antigen Specificity of Human Islet Infiltrating T Cells in Type 1 Diabetes
title_full Determining Antigen Specificity of Human Islet Infiltrating T Cells in Type 1 Diabetes
title_fullStr Determining Antigen Specificity of Human Islet Infiltrating T Cells in Type 1 Diabetes
title_full_unstemmed Determining Antigen Specificity of Human Islet Infiltrating T Cells in Type 1 Diabetes
title_short Determining Antigen Specificity of Human Islet Infiltrating T Cells in Type 1 Diabetes
title_sort determining antigen specificity of human islet infiltrating t cells in type 1 diabetes
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418007/
https://www.ncbi.nlm.nih.gov/pubmed/30906293
http://dx.doi.org/10.3389/fimmu.2019.00365
work_keys_str_mv AT nakayamamaki determiningantigenspecificityofhumanisletinfiltratingtcellsintype1diabetes
AT michelsaaronw determiningantigenspecificityofhumanisletinfiltratingtcellsintype1diabetes