Emerging immune therapies in type 1 diabetes and pancreatic islet transplantation

被引:10
|
作者
Schneider, D. A. [1 ]
Kretowicz, A. M. [1 ]
von Herrath, M. G. [1 ]
机构
[1] La Jolla Inst Allergy & Immunol, La Jolla, CA USA
来源
DIABETES OBESITY & METABOLISM | 2013年 / 15卷 / 07期
关键词
beta cell; clinical trial; diabetes mellitus; islets; transplantation; type; 1; diabetes; ANTI-CD3; MONOCLONAL-ANTIBODY; LOW-DOSE INTERLEUKIN-2; CD4(+)CD25(+) T-CELLS; LONG-TERM REMISSION; COMBINATION THERAPY; NOD MICE; ALPHA-1-ANTITRYPSIN TREATMENT; RESTORES NORMOGLYCEMIA; MULTIPLE-SCLEROSIS; B-LYMPHOCYTE;
D O I
10.1111/dom.12046
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In type 1 diabetes (T1D) the immune system attacks insulin-producing pancreatic -cells. Unfortunately, our ability to curb this pathogenic autoimmune response in a disease- and organ-specific manner is still very limited due to the inchoate understanding of the exact nature and the kinetics of the immunological pathomechanisms that lead to T1D. None of the clinical immune interventions thus far, which focused primarily on new-onset disease, were successful in producing lasting remission or curbing recurrent autoimmunity. However, these studies do provide us access to a tremendous amount of clinical data and specimens, which will aid us in revising our therapeutical approaches and defining the highly needed paradigm shift in T1D immunotherapy. Analysing the foundation and the results of the most current T1D immunotherapeutic trials, this article gives an outlook for future directions of the field.
引用
收藏
页码:581 / 592
页数:12
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