Volume 29, Issue 2 pp. 202-205
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Immunoreactive Polymorphonuclear Leukocyte Elastase in Complex with Alphal-Antitrypsin in Kawasaki Disease

Yasuzi Inamo M.D.

Corresponding Author

Yasuzi Inamo M.D.

Department of Pediatrics and Chemistry, Nihon University School of Medicine, and Department of Qinicopathology, Jichi Medical School, Tokyo and Tochigi

Department of Pediatrics, Nihon University School of Medicine, 30–1 Oyaguchi Kami-machi, Itabashi-ku, Tokyo 173, JapanSearch for more papers by this author
Kensuke Harada M.D.

Kensuke Harada M.D.

Department of Pediatrics and Chemistry, Nihon University School of Medicine, and Department of Qinicopathology, Jichi Medical School, Tokyo and Tochigi

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Masahiko Okuni M.D.

Masahiko Okuni M.D.

Department of Pediatrics and Chemistry, Nihon University School of Medicine, and Department of Qinicopathology, Jichi Medical School, Tokyo and Tochigi

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Kazuyoshi Kimoto M.D.

Kazuyoshi Kimoto M.D.

Department of Pediatrics and Chemistry, Nihon University School of Medicine, and Department of Qinicopathology, Jichi Medical School, Tokyo and Tochigi

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Shigeo Takeuchi M.D.

Shigeo Takeuchi M.D.

Department of Pediatrics and Chemistry, Nihon University School of Medicine, and Department of Qinicopathology, Jichi Medical School, Tokyo and Tochigi

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Ikunosuke Sakurabayashi M.D.

Ikunosuke Sakurabayashi M.D.

Department of Pediatrics and Chemistry, Nihon University School of Medicine, and Department of Qinicopathology, Jichi Medical School, Tokyo and Tochigi

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First published: April 1987
Citations: 11

This work was supported in part by a Grant-in-Aid for Scientific Research (59770698) from the Ministry of Education, Science and Culture, Japan.

Abstract

Immunoreactive polymorphonuclear leukocyte elastase (iPMN elastase) was measured by ELISA in 36 patients with Kawasaki disease and in 41 patients with anaphylactoid purpura and other infectious diseases of childhood. The iPMN elastase level was very high in Kawasaki disease compared with other diseases. There was no significant correlation in iPMN elastase levels in Kawasaki disease between the complicated and non-complicated groups in the acute period. The iPMN elastase in the non-complicated group fell below 250 4g/1 at 20 days from the onset of the illness. However, iPMN elastase in the complicated group (coronary aneurysm or dilatation) tended to remain high above 500 ligjl at 20 days from the onset. We suggest that increased iPMN elastase levels in Kawasaki disease reflect stronger enhancement and stimulation of PMN than in other diseases.

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