心肌炎
肌球蛋白
心肌病
分子模拟
心脏病
免疫学
发病机制
免疫系统
肽
生物
肌球蛋白轻链激酶
心力衰竭
抗原
炎症
医学
细胞生物学
内科学
生物化学
作者
Cristina Gil‐Cruz,Christian Perez‐Shibayama,Angelina De Martin,Francesca Ronchi,Katrien Van der Borght,Rebekka Niederer,Lucas Onder,Mechthild Lütge,Mario Novković,Veronika Nindl,Gustavo Ramos,Markus Arnoldini,Emma Slack,Valérie Boivin‐Jahns,Roland Jahns,Madeleine Wyss,Catherine Mooser,Bart N. Lambrecht,Micha T. Maeder,Hans Rickli
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2019-11-15
卷期号:366 (6467): 881-886
被引量:230
标识
DOI:10.1126/science.aav3487
摘要
Peptide mimicry breaks the heart Myocarditis, a prolonged chronic inflammation of heart muscle, can eventually progress to inflammatory cardiomyopathy, a serious condition associated with heart failure. Activated T helper (T H ) cells that recognize myosin heavy chain 6–derived peptides are thought to play a central role in this pathogenesis. Using a mouse model of myocarditis, Gil-Cruz et al. found that cardiac myosin–reactive T H cells are initially primed by myosin-peptide mimics derived from commensal Bacteroides species in the gut (see the Perspective by Epelman). Unlike heathy controls, human myocarditis patients also showed detectable immune reactivity to both Bacteroides and cardiac myosin antigens. Treatment with antibiotics dampened inflammatory responses and prevented lethal heart disease. Science , this issue p. 881 ; see also p. 806
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