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用于1型糖尿病病情改善的新型免疫疗法

Emerging Immunotherapies for Disease Modification of Type 1 Diabetes.

作者信息

Foster Timothy P, Bruggeman Brittany S, Haller Michael J

机构信息

Division of Endocrinology, Department of Pediatrics, College of Medicine, University of Florida, 1699 SW 16th Ave, Building A, Gainesville, FL, 32608, USA.

Department of Pathology, Immunology, and Laboratory Medicine, Diabetes Institute, University of Florida, Gainesville, FL, USA.

出版信息

Drugs. 2025 Apr;85(4):457-473. doi: 10.1007/s40265-025-02150-8. Epub 2025 Jan 28.

DOI:10.1007/s40265-025-02150-8
PMID:39873914
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11949705/
Abstract

Type 1 diabetes mellitus (T1DM) is characterized by the progressive, autoimmune-mediated destruction of β cells. As such, restoring immunoregulation early in the disease course is sought to retain endogenous insulin production. Nevertheless, in the more than 100 years since the discovery of insulin, treatment of T1DM has focused primarily on hormone replacement and glucose monitoring. That said, immunotherapies are widely used to interdict autoimmune and autoinflammatory diseases and are emerging as potential therapeutics seeking the preservation of β-cell function among those with T1DM. In the past 4 decades of diabetes research, several immunomodulatory therapies have been explored, culminating with the US Food and Drug Administration approval of teplizumab to delay stage 3 (clinical) onset of T1DM. Clinical trials seeking to prevent or reverse T1DM by repurposing immunotherapies approved for other autoimmune conditions and by exploring new therapeutics are ongoing. Collectively, these efforts have the potential to transform the future of diabetes care. We encapsulate the past 40 years of immunotherapy trials, take stock of our successes and failures, and chart paths forward in this new age of clinically available immune therapies for T1DM.

摘要

1型糖尿病(T1DM)的特征是β细胞进行性、自身免疫介导的破坏。因此,人们试图在疾病进程早期恢复免疫调节,以维持内源性胰岛素分泌。然而,自胰岛素发现以来的100多年里,T1DM的治疗主要集中在激素替代和血糖监测上。尽管如此,免疫疗法被广泛用于阻断自身免疫性和自身炎症性疾病,并且正在成为T1DM患者中寻求保留β细胞功能的潜在疗法。在过去40年的糖尿病研究中,已经探索了几种免疫调节疗法,最终美国食品药品监督管理局批准了替普珠单抗来延缓T1DM 3期(临床)发病。通过重新利用已批准用于其他自身免疫性疾病的免疫疗法以及探索新的疗法来预防或逆转T1DM的临床试验正在进行中。总体而言,这些努力有可能改变糖尿病护理的未来。我们总结了过去40年的免疫疗法试验,评估了我们的成功与失败,并在T1DM临床可用免疫疗法的这个新时代规划前进的道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bac0/11949705/e3b18c216d2b/nihms-2059931-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bac0/11949705/e35dfa84e807/nihms-2059931-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bac0/11949705/1c9593d890a6/nihms-2059931-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bac0/11949705/e3b18c216d2b/nihms-2059931-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bac0/11949705/e35dfa84e807/nihms-2059931-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bac0/11949705/1c9593d890a6/nihms-2059931-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bac0/11949705/e3b18c216d2b/nihms-2059931-f0003.jpg

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本文引用的文献

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Transplantation of chemically induced pluripotent stem-cell-derived islets under abdominal anterior rectus sheath in a type 1 diabetes patient.化学诱导多能干细胞源性胰岛在 1 型糖尿病患者腹部前正中线皮下的移植。
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Oral Insulin Delay of Stage 3 Type 1 Diabetes Revisited in HLA DR4-DQ8 Participants in the TrialNet Oral Insulin Prevention Trial (TN07).
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Consensus guidance for monitoring individuals with islet autoantibody-positive pre-stage 3 type 1 diabetes.胰岛自身抗体阳性的 3 期 1 型糖尿病前阶段患者监测的共识指南。
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A Golden Hour and Golden Opportunity for β-Cell Preservation.β细胞保护的黄金一小时与黄金机遇。
Diabetes. 2024 Jun 1;73(6):834-836. doi: 10.2337/dbi24-0019.
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A phase 2 randomized trial with autologous polyclonal expanded regulatory T cells in children with new-onset type 1 diabetes.一项自体多克隆扩增调节性 T 细胞治疗新发 1 型糖尿病儿童的 2 期随机试验。
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