Epigenetics of autoantigens: new opportunities for therapy of autoimmune diseases.

Genetics and Epigenetics Pub Date : 2013-10-29 eCollection Date: 2013-01-01 DOI:10.4137/GEG.S12144
Marko Radic, Sylviane Muller
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引用次数: 10

Abstract

The field of epigenetics requires that traditional divisions between scientific disciplines give way to cross-fertilization of concepts and ideas from different areas of investigation. Such is the case with research in autoimmunity. Recent discoveries of stimuli that induce autoimmunity reveal that epigenetic marks of autoantigens are recognized by autoreactive B and T cell receptors. Thus, insights into the initiation of autoimmunity, its prevention and therapy will arise from understanding the biochemistry, cell biology and microbiology of autoantigen epigenetics. Here, we highlight potential benefits from the inhibition of a histone modifying enzyme and the administration of a phosphorylated, spliceosome-derived peptide, in the treatment of autoimmunity.

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自身抗原的表观遗传学:自身免疫性疾病治疗的新机遇。
表观遗传学领域要求不同学科之间的传统划分让位于来自不同研究领域的概念和思想的相互融合。这就是自身免疫研究的情况。最近发现的刺激诱导自身免疫表明,自身抗原的表观遗传标记被自身反应性B细胞和T细胞受体识别。因此,对自身免疫的起源、预防和治疗的深入了解将源于对自身抗原表观遗传学的生物化学、细胞生物学和微生物学的理解。在这里,我们强调了抑制组蛋白修饰酶和使用磷酸化剪接体衍生肽治疗自身免疫的潜在益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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