Section on Immunobiology at the Joslin Diabetes Center, Harvard Medical School, Boston, MA 02215, USA.
Trends Cardiovasc Med. 2012 Jul;22(5):113-7. doi: 10.1016/j.tcm.2012.07.005. Epub 2012 Aug 16.
For more than a half century, autoimmunity has been linked to a diverse array of heart diseases, including rheumatic carditis, myocarditis, Chagas' cardiomyopathy, post-myocardial infarction (Dressler's) syndrome, and idiopathic dilated cardiomyopathy. Why the heart is targeted by autoimmunity in these seemingly unrelated conditions has remained enigmatic. Here, we discuss our recent studies indicating that this susceptibility is mediated by impaired negative selection of autoreactive α-myosin heavy-chain-specific CD4(+) T cells in the thymus of both mice and humans. We describe how this process may place the heart at increased risk for autoimmune attack following ischemic or infectious injury, providing a rationale for the development of antigen-specific tolerogenic therapies.
半个多世纪以来,自身免疫与多种心脏病相关,包括风湿性心内膜炎、心肌炎、恰加斯心肌病、心肌梗死后(Dressler)综合征和特发性扩张型心肌病。在这些看似无关的情况下,为什么自身免疫会针对心脏,这仍然是个谜。在这里,我们讨论了我们最近的研究结果,表明这种易感性是由小鼠和人类胸腺中自身反应性α-肌球蛋白重链特异性 CD4(+) T 细胞的负选择受损所介导的。我们描述了这一过程如何使心脏在缺血或感染性损伤后更容易受到自身免疫攻击,并为抗原特异性免疫耐受治疗的发展提供了依据。