Potential for anti-DNA immunoglobulin peptide therapy in systemic lupus erythematosus

被引:0
|
作者
Iikuni, Noriko [1 ]
Hahn, Bevra H. [1 ]
La Cava, Antonio [1 ]
机构
[1] Univ Calif Los Angeles, Div Rheumatol, Dept Med, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
anti DNA antibodies; peptide; immunotherapy; systemic lupus erythematosus; REGULATORY T-CELLS; COMPLEMENTARITY-DETERMINING REGION-1; BOUND SELF PEPTIDES; PHASE-II TRIAL; X NZW)F-1 MICE; MURINE LUPUS; MULTIPLE-SCLEROSIS; NUCLEOSOMAL PEPTIDES; AUTOIMMUNE-DISEASES; AMELIORATES LUPUS;
D O I
10.1517/14712590802681636
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
Background: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease with elevated morbidity and multi-organ involvement. While many strategies have shown efficacy and improved management of SLE, they have often been associated with adverse effects. Some patients may not respond well to some treatments because of inter-individual variability of the disease. More specific and safer therapies are needed. Objective/methods: To review literature on peptide-based therapy of SLE. Results/conclusions: Recently, emphasis has been placed on targeting molecules and pathways involved in the inflammatory response in SLE, including the use of immunogenic peptides derived from anti-DNA antibodies. Encouraging data from murine models of SLE have led to tests in initial clinical trials in humans - which have unfortunately not met the primary endpoints. The current challenge is to design improved strategies for immunotherapeutic use of anti-DNA peptides in SLE.
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页码:201 / 206
页数:6
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