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1 型糖尿病 (T1D) 治疗中的最佳耐受原性树突状细胞:我们可以从非肥胖型糖尿病 (NOD) 小鼠模型中学到什么?

Optimal Tolerogenic Dendritic Cells in Type 1 Diabetes (T1D) Therapy: What Can We Learn From Non-obese Diabetic (NOD) Mouse Models?

机构信息

Institute of Microbiology of the Czech Academy of Sciences, v.v.i., Prague, Czechia.

SOTIO a s., Prague, Czechia.

出版信息

Front Immunol. 2019 May 14;10:967. doi: 10.3389/fimmu.2019.00967. eCollection 2019.


DOI:10.3389/fimmu.2019.00967
PMID:31139178
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6527741/
Abstract

Tolerogenic dendritic cells (tolDCs) are explored as a promising standalone or combination therapy in type 1 diabetes (T1D). The therapeutic application of tolDCs, including in human trials, has been tested also in other autoimmune diseases, however, T1D displays some unique features. In addition, unlike in several disease-induced animal models of autoimmune diseases, the prevalent animal model for T1D, the NOD mouse, develops diabetes spontaneously. This review compares evidence of various tolDCs approaches obtained from animal (mainly NOD) models of T1D with a focus on parameters of this cell-based therapy such as protocols of tolDC preparation, antigen-specific . unspecific approaches, doses of tolDCs and/or autoantigens, application schemes, application routes, the migration of tolDCs as well as their preventive, early pre-onset intervention or curative effects. This review also discusses perspectives of tolDC therapy and areas of preclinical research that are in need of better clarification in animal models in a quest for effective and optimal tolDC therapies of T1D in humans.

摘要

耐受性树突状细胞(tolDCs)被探索作为 1 型糖尿病(T1D)的一种有前途的独立或联合治疗方法。tolDCs 的治疗应用,包括临床试验,也已经在其他自身免疫性疾病中进行了测试,然而,T1D 具有一些独特的特征。此外,与几种自身免疫性疾病诱导的动物模型不同,T1D 的常见动物模型 NOD 小鼠会自发发生糖尿病。本综述比较了从 T1D 的动物(主要是 NOD)模型中获得的各种 tolDC 方法的证据,重点关注这种基于细胞的治疗方法的参数,如 tolDC 制备方案、抗原特异性和非特异性方法、tolDCs 和/或自身抗原的剂量、应用方案、应用途径、tolDC 的迁移以及它们的预防、早期发病前干预或治疗效果。本综述还讨论了 tolDC 治疗的前景和临床前研究领域,这些领域在动物模型中需要更好地阐明,以寻求人类 T1D 的有效和最佳 tolDC 治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f29/6527741/b8a9559e59dc/fimmu-10-00967-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f29/6527741/b8a9559e59dc/fimmu-10-00967-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f29/6527741/b8a9559e59dc/fimmu-10-00967-g0001.jpg

相似文献

[1]
Optimal Tolerogenic Dendritic Cells in Type 1 Diabetes (T1D) Therapy: What Can We Learn From Non-obese Diabetic (NOD) Mouse Models?

Front Immunol. 2019-5-14

[2]
Antigen Loading (e.g., Glutamic Acid Decarboxylase 65) of Tolerogenic DCs (tolDCs) Reduces Their Capacity to Prevent Diabetes in the Non-Obese Diabetes (NOD)-Severe Combined Immunodeficiency Model of Adoptive Cotransfer of Diabetes As Well As in NOD Mice.

Front Immunol. 2018-2-16

[3]
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[4]
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[5]
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[6]
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[7]
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[10]
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引用本文的文献

[1]
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Front Drug Deliv. 2024-8-8

[2]
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Epigenomics. 2025-6

[3]
Tolerogenic dendritic cells in type 1 diabetes: no longer a concept.

Front Immunol. 2023

[4]
Dendritic Cells and Their Immunotherapeutic Potential for Treating Type 1 Diabetes.

Int J Mol Sci. 2022-4-28

[5]
Syngeneic bone marrow transplantation in combination with PI3K inhibitor reversed hyperglycemia in later-stage streptozotocin-induced diabetes.

Ann Transl Med. 2021-11

[6]
Current advances in using tolerogenic dendritic cells as a therapeutic alternative in the treatment of type 1 diabetes.

World J Diabetes. 2021-5-15

[7]
Regulatory Dendritic Cells, T Cell Tolerance, and Dendritic Cell Therapy for Immunologic Disease.

Front Immunol. 2021

[8]
Immunomodulation for optimal cardiac regeneration: insights from comparative analyses.

NPJ Regen Med. 2021-2-15

[9]
Role of the PD-1/PD-L1 Dyad in the Maintenance of Pancreatic Immune Tolerance for Prevention of Type 1 Diabetes.

Front Endocrinol (Lausanne). 2020

[10]
Clinical Use of Antigens as Novel Immunotherapies for Autoimmune Disorders.

Front Immunol. 2020

本文引用的文献

[1]
Cell Based Therapy for Type 1 Diabetes: Should We Take Hyperglycemia Into Account?

Front Immunol. 2019-2-5

[2]
Comparison of dendritic cells obtained from autoimmunty-prone and resistant rats.

Immunobiology. 2019-2-8

[3]
Vitamin D controls the capacity of human dendritic cells to induce functional regulatory T cells by regulation of glucose metabolism.

J Steroid Biochem Mol Biol. 2018-11-24

[4]
Neoepitopes: a new take on beta cell autoimmunity in type 1 diabetes.

Diabetologia. 2018-11-6

[5]
Prevention of Type 1 Diabetes with Acetalated Dextran Microparticles Containing Rapamycin and Pancreatic Peptide P31.

Adv Healthc Mater. 2018-7-26

[6]
A Future for Autologous Hematopoietic Stem Cell Transplantation in Type 1 Diabetes.

Front Immunol. 2018-4-6

[7]
Bags versus flasks: a comparison of cell culture systems for the production of dendritic cell-based immunotherapies.

Transfusion. 2018-7

[8]
Immature Dendritic Cell Therapy Confers Durable Immune Modulation in an Antigen-Dependent and Antigen-Independent Manner in Nonobese Diabetic Mice.

J Immunol Res. 2018-2-14

[9]
Antigen Loading (e.g., Glutamic Acid Decarboxylase 65) of Tolerogenic DCs (tolDCs) Reduces Their Capacity to Prevent Diabetes in the Non-Obese Diabetes (NOD)-Severe Combined Immunodeficiency Model of Adoptive Cotransfer of Diabetes As Well As in NOD Mice.

Front Immunol. 2018-2-16

[10]
Tolerance through Education: How Tolerogenic Dendritic Cells Shape Immunity.

Front Immunol. 2017-12-11

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