Radic Marko, Muller Sylviane
Department of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science Center, Memphis, TN, USA.
Immunopathology and therapeutic chemistry/Laboratory of excellence MEDALIS, Institut de Biologie Moléculaire et Cellulaire, CNRS, Strasbourg, France.
Genet Epigenet. 2013 Oct 29;5:63-70. doi: 10.4137/GEG.S12144. eCollection 2013.
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.
表观遗传学领域要求科学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交叉融合。自身免疫研究就是如此。最近关于诱导自身免疫的刺激因素的发现表明,自身抗原的表观遗传标记可被自身反应性B和T细胞受体识别。因此,对自身免疫的起始、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。在此,我们强调抑制一种组蛋白修饰酶以及给予一种磷酸化的、剪接体衍生肽在自身免疫治疗中的潜在益处。