Heat-shock protein 60 as a tool for novel therapeutic strategies that target the induction of regulatory T cells in human arthritis

被引:18
作者
Kamphuis, Sylvia
Albani, Salvatore
Prakken, Berent J.
机构
[1] Univ Med Ctr Utrecht, Dept Paediat Immunol, NL-3508 AB Utrecht, Netherlands
[2] Wilhelmina Childrens Hosp, IACOPO Inst Translat Med, Utrecht, Netherlands
[3] Erasmus MC Sophia, Dept Paediat Immunol & Rheumatol, Rotterdam, Netherlands
[4] Univ Calif San Diego, Dept Med & Paediat, San Diego, CA 92103 USA
[5] IACOPO Inst Translat Med, San Diego, CA USA
[6] Androclus Therapeut, I-92100 Milan, Italy
关键词
antigen-specific immunotherapy; arthritis; autoimmune disease; heat-shock protein 60; JIA; regulatory T cell;
D O I
10.1517/14712598.6.6.579
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In health, immune responses to self are abundantly available, but under strict control of mechanisms of peripheral tolerance. Occasionally the immune system loses control and an autoimmune disease develops. At present, treatment of autoimmune disease is based on generalised suppression of all immune responses, and is often needed to be lifelong, leading to long-term toxicities and suppression of protective immune responses against pathogens. A more targeted approach would be to reset the immune system via restoration of failing regulatory mechanisms, and redirect the immune system to a state of tolerance. Over the past decade there have been enormous advances in the understanding of basic processes that control immune tolerance, pushing regulatory T cells forward as targets for novel therapeutic strategies. This review describes the development of antigen-specific immunotherapy that targets the antigen-specific induction of regulatory T cells as a means to treat autoimmune disease. The 'holy grail' for autoimmunity is not the disease-causing antigen, but the disease-curing antigen.
引用
收藏
页码:579 / 589
页数:11
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