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Systemic autoimmunity induced by the TLR7/8 agonist Resiquimod causes myocarditis and dilated cardiomyopathy in a new mouse model of autoimmune heart disease

机译:由TLR7 / 8激动剂瑞西莫德诱导的全身性自身免疫在新的自身免疫性心脏病小鼠模型中引起心肌炎和扩张型心肌病

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Systemic autoimmune diseases such as systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA) show significant heart involvement and cardiovascular morbidity, which can be due to systemically increased levels of inflammation or direct autoreactivity targeting cardiac tissue. Despite high clinical relevance, cardiac damage secondary to systemic autoimmunity lacks inducible rodent models. Here, we characterise immune-mediated cardiac tissue damage in a new model of SLE induced by topical application of the Toll-like receptor 7/8 (TLR7/8) agonist Resiquimod. We observe a cardiac phenotype reminiscent of autoimmune-mediated dilated cardiomyopathy, and identify auto-antibodies as major contributors to cardiac tissue damage. Resiquimod-induced heart disease is a highly relevant mouse model for mechanistic and therapeutic studies aiming to protect the heart during autoimmunity.
机译:系统性自身免疫性疾病,例如系统性红斑狼疮(SLE)和类风湿性关节炎(RA),显示出明显的心脏受累和心血管疾病,这可能是由于炎症水平升高或靶向心脏组织的直接自身反应性引起的。尽管具有高度的临床相关性,但全身性自身免疫性继发的心脏损害缺乏可诱导的啮齿动物模型。在这里,我们表征了由局部应用Toll样受体7/8(TLR7 / 8)激动剂瑞西莫特诱导的SLE新模型中免疫介导的心脏组织损伤。我们观察到的心脏表型让人联想到自身免疫介导的扩张型心肌病,并确定自身抗体是造成心脏组织损伤的主要因素。瑞喹莫德诱发的心脏病是用于机制和治疗研究的高度相关的小鼠模型,旨在在自身免疫过程中保护心脏。

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