Autoimmune Dilated Cardiomyopathy in PD-1 Receptor-Deficient Mice

Author:

Nishimura Hiroyuki1,Okazaki Taku1,Tanaka Yoshimasa2,Nakatani Kazuki3,Hara Masatake4,Matsumori Akira4,Sasayama Shigetake4,Mizoguchi Akira5,Hiai Hiroshi6,Minato Nagahiro2,Honjo Tasuku1

Affiliation:

1. Department of Medical Chemistry,

2. Department of Immunology and Cell Biology,

3. Second Department of Anatomy, Osaka City University Medical School, 1-4-3 Asahi-Machi, Abeno-Ku, Osaka, 545-8585, Japan.

4. Department of Cardiovascular Medicine,

5. Department of Anatomy and Neurobiology,

6. Department of Pathology and Biology of Diseases, Graduate School of Medicine, Kyoto University, Yoshida Konoe-cho, Sakyo, Kyoto, 606-8501, Japan.

Abstract

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference26 articles.

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3. J. D. Hosenpud J. A. Jarcho in Congestive Heart Failure J. D. Hosenpud B. H. Greenberg Eds. (Lippincott William & Wilkins Philadelphia ed. 2 2000) p. 281.

4. Caforio A. L. P., et al., Lancet 344, 773 (1994);

5. Magnusson Y., et al., J. Clin. Invest. 86, 1658 (1990).

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