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Biomarkers for immune intervention trials in type 1 diabetes
被引:26
|作者:
Mallone, Roberto
[1
,2
,3
]
Roep, Bart O.
[4
,5
]
机构:
[1] DeAR Lab Avenir, INSERM U1016, Cochin Inst, Paris, France
[2] Paris Descartes Univ, Sorbonne Paris Cite, Fac Med, Paris, France
[3] Hop Hotel Dieu, Assistance Publ Hop Paris, Serv Diabetol, Paris, France
[4] Leiden Univ, Med Ctr, Dept Immunohaematol & Blood Transfus, Leiden, Netherlands
[5] Natl Diabet Expert Ctr, Leiden, Netherlands
基金:
欧盟第七框架计划;
关键词:
Autoantibodies;
C-peptide;
Endpoint;
T cells;
T-CELL RESPONSES;
ISLET ALLOGRAFTS;
PERIPHERAL-BLOOD;
RECENT-ONSET;
PHASE-II;
INSULIN;
TRANSPLANTATION;
PROINSULIN;
IMMUNOLOGY;
WORKSHOP;
D O I:
10.1016/j.clim.2013.02.009
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
After many efforts to improve and standardize assays for detecting immune biomarkers in type 1 diabetes (T1D), methods to identify and monitor such correlates of insulitis are coming of age. The ultimate goal is to use these correlates to predict disease progression before onset and regression following therapeutic intervention, which would allow performing smaller and shorter pilot clinical trials with earlier endpoints than those offered by preserved beta-cell function or improved glycemic control. Here, too, progress has been made. With the emerging insight that T1D represents a heterogeneous disease, the next challenge is to define patient subpopulations that qualify for personalized medicine or that should be enrolled for immune intervention, to maximize clinical benefit and decrease collateral damage by ineffective or even adverse immune therapeutics. This review discusses the current state of the art, setting the stage for future efforts to monitor disease heterogeneity, progression and therapeutic intervention in T1D. (C) 2013 Elsevier Inc. All rights reserved.
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页码:286 / 296
页数:11
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