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1
Surrogate end points in the design of immunotherapy trials: emerging lessons from type 1 diabetes.免疫治疗试验设计中的替代终点:1 型糖尿病带来的新教训。
Nat Rev Immunol. 2010 Feb;10(2):145-52. doi: 10.1038/nri2705.
2
Failure to preserve beta-cell function with mycophenolate mofetil and daclizumab combined therapy in patients with new- onset type 1 diabetes.霉酚酸酯和达克珠单抗联合治疗新发 1 型糖尿病患者β细胞功能丧失。
Diabetes Care. 2010 Apr;33(4):826-32. doi: 10.2337/dc09-1349. Epub 2010 Jan 12.
3
Rituximab, B-lymphocyte depletion, and preservation of beta-cell function.利妥昔单抗、B淋巴细胞清除与β细胞功能的保留
N Engl J Med. 2009 Nov 26;361(22):2143-52. doi: 10.1056/NEJMoa0904452.
4
Effects of exenatide alone and in combination with daclizumab on beta-cell function in long-standing type 1 diabetes.艾塞那肽单药及联合地昔单抗治疗对长期 1 型糖尿病患者胰岛β细胞功能的影响。
Diabetes Care. 2009 Dec;32(12):2251-7. doi: 10.2337/dc09-0773. Epub 2009 Oct 6.
5
Genetic-induced variations in the GAD65 T-cell repertoire governs efficacy of anti-CD3/GAD65 combination therapy in new-onset type 1 diabetes.遗传诱导的 GAD65 T 细胞库变化可调控抗 CD3/GAD65 联合治疗新诊断 1 型糖尿病的疗效。
Mol Ther. 2010 Feb;18(2):307-16. doi: 10.1038/mt.2009.197. Epub 2009 Aug 18.
6
Validity and reproducibility of measurement of islet autoreactivity by T-cell assays in subjects with early type 1 diabetes.胰岛自身反应性 T 细胞检测在早期 1 型糖尿病患者中的测量的有效性和可重复性。
Diabetes. 2009 Nov;58(11):2588-95. doi: 10.2337/db09-0249. Epub 2009 Aug 12.
7
Treatment of patients with new onset Type 1 diabetes with a single course of anti-CD3 mAb Teplizumab preserves insulin production for up to 5 years.采用单疗程抗CD3单克隆抗体替普珠单抗治疗新发1型糖尿病患者,可使胰岛素分泌维持长达5年。
Clin Immunol. 2009 Aug;132(2):166-73. doi: 10.1016/j.clim.2009.04.007. Epub 2009 May 14.
8
How can we improve the translational landscape for a faster cure of type 1 diabetes?我们如何改善转化医学前景以更快治愈1型糖尿病?
J Clin Invest. 2009 May;119(5):1061-5. doi: 10.1172/jci37593.
9
Analysis of islet inflammation in human type 1 diabetes.人类1型糖尿病中胰岛炎症的分析。
Clin Exp Immunol. 2009 Feb;155(2):173-81. doi: 10.1111/j.1365-2249.2008.03860.x.
10
Post-mortem analysis of islet pathology in type 1 diabetes illuminates the life and death of the beta cell.1型糖尿病胰岛病理的尸检分析揭示了β细胞的生死。
Clin Exp Immunol. 2009 Feb;155(2):125-7. doi: 10.1111/j.1365-2249.2008.03864.x.

开发 1 型糖尿病联合免疫疗法:来自 ITN-JDRF 1 型糖尿病联合治疗评估小组的建议。

Developing combination immunotherapies for type 1 diabetes: recommendations from the ITN-JDRF Type 1 Diabetes Combination Therapy Assessment Group.

机构信息

Immune Tolerance Network, San Francisco, CA 94107, USA.

出版信息

Clin Exp Immunol. 2010 May;160(2):176-84. doi: 10.1111/j.1365-2249.2010.04153.x.

DOI:10.1111/j.1365-2249.2010.04153.x
PMID:20629979
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2857940/
Abstract

Like many other complex human disorders of unknown aetiology, autoimmune-mediated type 1 diabetes may ultimately be controlled via a therapeutic approach that combines multiple agents, each with differing modes of action. The numerous advantages of such a strategy include the ability to minimize toxicities and realize synergies to enhance and prolong efficacy. The recognition that combinations might offer far-reaching benefits, at a time when few single agents have yet proved themselves in well-powered trials, represents a significant challenge to our ability to conceive and implement rational treatment designs. As a first step in this process, the Immune Tolerance Network, in collaboration with the Juvenile Diabetes Research Foundation, convened a Type 1 Diabetes Combination Therapy Assessment Group, the recommendations of which are discussed in this Perspective paper.

摘要

与许多其他病因不明的复杂人类疾病一样,自身免疫介导的 1 型糖尿病最终可能通过一种联合治疗方法得到控制,这种方法结合了多种具有不同作用机制的药物。这种策略有许多优点,包括能够最大限度地减少毒性并实现协同作用,以增强和延长疗效。在很少有单一药物在大型试验中证明有效的情况下,认识到联合治疗可能带来深远的益处,这对我们构思和实施合理治疗方案的能力构成了重大挑战。作为这一过程的第一步,免疫耐受网络与青少年糖尿病研究基金会合作,召集了 1 型糖尿病联合治疗评估小组,本文讨论了该小组的建议。