id paper:paper_10217401_v17_n3_p173_Castro
record_format dspace
spelling paper:paper_10217401_v17_n3_p173_Castro2023-06-08T16:00:01Z Disease-modifying immunotherapy for the management of autoimmune diabetes Dendritic cells Immunoregulation Type 1 diabetes autoimmune disease autoimmunity cell activity cell clone cell cloning cell destruction cell disruption conference paper dendritic cell disease course human immunomodulation immunoregulation immunotherapy inner cell mass insulin dependent diabetes mellitus lymphocyte preservation nonhuman pancreas islet beta cell priority journal regulatory T lymphocyte T lymphocyte Animals Antirheumatic Agents Autoimmunity Dendritic Cells Diabetes Mellitus, Type 1 Disease Models, Animal Humans Immunomodulation Immunotherapy Insulin-Secreting Cells T-Lymphocytes, Helper-Inducer Type 1 diabetes (T1D) is a T cell-mediated autoimmune disease that destroys the insulin-secreting β-cells of the pancreas. It is now possible to predict those candidates that will progress to T1D before the full onset of the disease. Prevention of uncontrollable autoimmunity against β-cells in therapies for T1D is mandatory to preserve the β-cell mass. Therefore, immunomodulatory strategies directed to inhibiting the activity of self-reactive T cell clones as well as induction of regulatory T cells would be beneficial for prevention of T1D or recurrence of β-cell autoimmunity against islet cell allografts. © 2010 S. Karger AG, Basel. 2010 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_10217401_v17_n3_p173_Castro http://hdl.handle.net/20.500.12110/paper_10217401_v17_n3_p173_Castro
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Dendritic cells
Immunoregulation
Type 1 diabetes
autoimmune disease
autoimmunity
cell activity
cell clone
cell cloning
cell destruction
cell disruption
conference paper
dendritic cell
disease course
human
immunomodulation
immunoregulation
immunotherapy
inner cell mass
insulin dependent diabetes mellitus
lymphocyte preservation
nonhuman
pancreas islet beta cell
priority journal
regulatory T lymphocyte
T lymphocyte
Animals
Antirheumatic Agents
Autoimmunity
Dendritic Cells
Diabetes Mellitus, Type 1
Disease Models, Animal
Humans
Immunomodulation
Immunotherapy
Insulin-Secreting Cells
T-Lymphocytes, Helper-Inducer
spellingShingle Dendritic cells
Immunoregulation
Type 1 diabetes
autoimmune disease
autoimmunity
cell activity
cell clone
cell cloning
cell destruction
cell disruption
conference paper
dendritic cell
disease course
human
immunomodulation
immunoregulation
immunotherapy
inner cell mass
insulin dependent diabetes mellitus
lymphocyte preservation
nonhuman
pancreas islet beta cell
priority journal
regulatory T lymphocyte
T lymphocyte
Animals
Antirheumatic Agents
Autoimmunity
Dendritic Cells
Diabetes Mellitus, Type 1
Disease Models, Animal
Humans
Immunomodulation
Immunotherapy
Insulin-Secreting Cells
T-Lymphocytes, Helper-Inducer
Disease-modifying immunotherapy for the management of autoimmune diabetes
topic_facet Dendritic cells
Immunoregulation
Type 1 diabetes
autoimmune disease
autoimmunity
cell activity
cell clone
cell cloning
cell destruction
cell disruption
conference paper
dendritic cell
disease course
human
immunomodulation
immunoregulation
immunotherapy
inner cell mass
insulin dependent diabetes mellitus
lymphocyte preservation
nonhuman
pancreas islet beta cell
priority journal
regulatory T lymphocyte
T lymphocyte
Animals
Antirheumatic Agents
Autoimmunity
Dendritic Cells
Diabetes Mellitus, Type 1
Disease Models, Animal
Humans
Immunomodulation
Immunotherapy
Insulin-Secreting Cells
T-Lymphocytes, Helper-Inducer
description Type 1 diabetes (T1D) is a T cell-mediated autoimmune disease that destroys the insulin-secreting β-cells of the pancreas. It is now possible to predict those candidates that will progress to T1D before the full onset of the disease. Prevention of uncontrollable autoimmunity against β-cells in therapies for T1D is mandatory to preserve the β-cell mass. Therefore, immunomodulatory strategies directed to inhibiting the activity of self-reactive T cell clones as well as induction of regulatory T cells would be beneficial for prevention of T1D or recurrence of β-cell autoimmunity against islet cell allografts. © 2010 S. Karger AG, Basel.
title Disease-modifying immunotherapy for the management of autoimmune diabetes
title_short Disease-modifying immunotherapy for the management of autoimmune diabetes
title_full Disease-modifying immunotherapy for the management of autoimmune diabetes
title_fullStr Disease-modifying immunotherapy for the management of autoimmune diabetes
title_full_unstemmed Disease-modifying immunotherapy for the management of autoimmune diabetes
title_sort disease-modifying immunotherapy for the management of autoimmune diabetes
publishDate 2010
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_10217401_v17_n3_p173_Castro
http://hdl.handle.net/20.500.12110/paper_10217401_v17_n3_p173_Castro
_version_ 1768544649750773760