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Administration of human immunoglobulin suppresses development of murine systemic vasculitis induced with Candida albicans water-soluble fraction: an animal model of Kawasaki disease.

Abstract
We investigated the inhibitory effect of human immunoglobulin (h-Ig) on the development of coronary arteritis in a murine model of vasculitis induced with a Candida albicans water-soluble fraction (CAWS). CAWS was intraperitoneally injected to C57BL/6 mice for 5 days. Then h-Ig was administered according to various schedules. The animals were sacrificed in week 5, and the status of vasculitis in the coronary arteries and the aortic root was investigated histologically. The groups in which h-Ig was administered for 5 days from day 3 and from day 5 of the experiment showed a significant reduction in the incidence of panvasculitis. In addition, the scope and severity of the inflammation of the aortic root and the coronary arteries were reduced in both groups. In the group administered h-Ig for 5 days from day 1 and the group administered a high dose of h-Ig once on day 1 or day 3, no suppression of development of vasculitis was observed. The h-Ig acted by suppressing the generation and progression of vasculitis in this CAWS-induced murine vasculitis model.
AuthorsKei Takahashi, Toshiaki Oharaseki, Yuki Yokouchi, Noriko N Miura, Naohito Ohno, Akiko I Okawara, Hisao Murata, Shiro Naoe, Kazuo Suzuki
JournalModern rheumatology (Mod Rheumatol) Vol. 20 Issue 2 Pg. 160-7 (Apr 2010) ISSN: 1439-7609 [Electronic] England
PMID19943075 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antigens, Fungal
  • Immunoglobulins, Intravenous
Topics
  • Animals
  • Antigens, Fungal
  • Arteritis (immunology, pathology, prevention & control)
  • Candida albicans
  • Coronary Artery Disease (immunology, pathology, prevention & control)
  • Disease Models, Animal
  • Humans
  • Immunization, Passive
  • Immunoglobulins, Intravenous (therapeutic use)
  • Male
  • Mice
  • Mice, Inbred A
  • Mice, Inbred C57BL
  • Mucocutaneous Lymph Node Syndrome (immunology)
  • Time Factors

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