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PMID: 11472393 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Enhanced expression and production of monocyte chemoattractant protein-1 in myocarditis.

Clinical and experimental immunology ·Vol. 124 ·No. 3 ·2001-06-00 ·Pages 346-52

Fuse K, Kodama M, Hanawa H, Okura Y, Ito M, Shiono T, Maruyama S, Hirono S, Kato K, Watanabe K, Aizawa Y

Abstract

Monocyte chemoattractant protein-1 (MCP-1) is a member of the C-C chemokine family that has been shown to play a major role in the migration of monocytes and T cells to an inflammatory focus. To clarify the role of MCP-1 in the pathogenesis of myocarditis, we have examined the expression of MCP-1 in rat hearts with experimental autoimmune myocarditis (EAM), and have also measured serum levels of MCP-1 in patients with histology-proven acute myocarditis. Lewis rats were immunized with cardiac myosin and were killed 9, 12, 15, 18, 21, 24, 27, 30, 33, 36, 42 and 56 days after immunization. Large mononuclear cells in the myocardial interstitium were stained with an anti-MCP-1 antibody. mRNA of MCP-1 increased in the hearts of EAM rats from days 15--27 as shown by quantitative reverse transcription-polymerase chain reaction. Serum MCP-1 levels of the rats with EAM were significantly elevated from days 15--24. In the clinical study, serum levels of MCP-1 in 24 patients with acute myocarditis at the time of admission (165.2 +/- 55.8 pg/ml) were significantly (P = 0.0301) elevated compared with those of 20 healthy volunteers (61.8 +/- 10.7 pg/ml). Serum MCP-1 levels of 8 fatal cases (371.8 +/- 145.2 pg/ml) were significantly (P = 0.0058) higher than those of 16 cases who survived (65.5 +/- 12.8 pg/ml). In conclusions, MCP-1 may play an important role in the pathogenesis of human acute myocarditis as well as in the progression of rat EAM.

MeSH Terms
Acute Disease Animals Chemokine CCL2/biosynthesis,blood,genetics Disease Models, Animal Gene Expression Humans Immunohistochemistry/methods Myocarditis/blood,immunology Myocardium/pathology RNA, Messenger Rats Rats, Inbred Lew
Chemicals
Chemokine CCL2 RNA, Messenger
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Fuse K
The First Department of Internal Medicine, Niigata University School of Medicine, Niigata, Japan. [email protected]
Kodama M
Hanawa H
Okura Y
Ito M
Shiono T
Maruyama S
Hirono S
Kato K
Watanabe K
Aizawa Y
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Article Info
Journal
Clinical and experimental immunology
Abbr.
Clin Exp Immunol
ISSN
0009-9104
Published
2001-06-00
Pages
346-52
Language
English
Region
England
NLM ID
0057202
PMCID
PMC1906075
Subset
IM
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