Nishimura H, Okazaki T, Tanaka Y, Nakatani K, Hara M, Matsumori A, Sasayama S, Mizoguchi A, Hiai H, Minato N, Honjo T
Department of Medical Chemistry, Graduate School of Medicine, Kyoto University, Yoshida Konoe-cho, Sakyo, Kyoto, 606-8501, Japan.
Science. 2001 Jan 12;291(5502):319-22. doi: 10.1126/science.291.5502.319.
Dilated cardiomyopathy is a severe pathology of the heart with poorly understood etiology. Disruption of the gene encoding the negative immunoregulatory receptor PD-1 in BALB/c mice, but not in BALB/c RAG-2-/- mice, caused dilated cardiomyopathy with severely impaired contraction and sudden death by congestive heart failure. Affected hearts showed diffuse deposition of immunoglobulin G (IgG) on the surface of cardiomyocytes. All of the affected PD-1-/- mice exhibited high-titer circulating IgG autoantibodies reactive to a 33-kilodalton protein expressed specifically on the surface of cardiomyocytes. These results indicate that PD-1 may be an important factor contributing to the prevention of autoimmune diseases.
扩张型心肌病是一种病因尚不明确的严重心脏疾病。在BALB/c小鼠中,编码负性免疫调节受体PD-1的基因发生破坏会导致扩张型心肌病,伴有严重的收缩功能受损,并因充血性心力衰竭而猝死,但在BALB/c RAG-2 -/-小鼠中则不会出现这种情况。受影响的心脏显示免疫球蛋白G(IgG)在心肌细胞表面弥漫性沉积。所有受影响的PD-1 -/-小鼠都表现出高滴度的循环IgG自身抗体,这些抗体与心肌细胞表面特异性表达的一种33千道尔顿蛋白发生反应。这些结果表明,PD-1可能是预防自身免疫性疾病的一个重要因素。