Antigen-Based Immune Therapeutics for Type 1 Diabetes: Magic Bullets or Ordinary Blanks?

被引:27
作者
Culina, Slobodan [1 ,2 ]
Boitard, Christian [1 ,2 ,3 ]
Mallone, Roberto [1 ,2 ,3 ]
机构
[1] Hop St Vincent de Paul, INSERM, U986, DeAR Lab Avenir, F-75674 Paris 14, France
[2] Univ Paris 05, F-75006 Paris, France
[3] Hop Hotel Dieu, Assistance Publ Hop Paris, Serv Diabetol, F-75181 Paris, France
来源
CLINICAL & DEVELOPMENTAL IMMUNOLOGY | 2011年
关键词
BETA-CELL FUNCTION; ALTERED-PEPTIDE LIGAND; REGULATORY T-CELLS; PHASE-II TRIAL; RANDOMIZED CONTROLLED-TRIAL; MYELOID SUPPRESSOR-CELLS; DENDRITIC CELLS; NOD MICE; IN-VIVO; RECENT-ONSET;
D O I
10.1155/2011/286248
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The ideal drug ofmodern medicine is the one that achieves its therapeutic target with minimal adverse effects. Immune therapy of Type 1 diabetes (T1D) is no exception, and knowledge of the antigens targeted by pathogenic T cells offers a unique opportunity towards this goal. Different antigen formulations are being considered, such as proteins or peptides, either in their native form or modified ad hoc, DNA plasmids, and cell-based agents. Translation from mouse to human should take into account important differences, particularly in the time scale of autoimmune progression, and intervention. Critical parameters such as administration route, dosing and interval remain largely empirical and need to be further dissected. T1D staging through immune surrogate markers before and after treatment will be key in understanding therapeutic actions and to finally turn ordinary blanks into magic bullets.
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页数:15
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