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Nephrology Dialysis Transplantation, Vol 14, Issue 1 76-80, Copyright © 1999 by Oxford University Press


ORIGINAL ARTICLES

Eotaxin contributes to renal interstitial eosinophilia

T Wada, K Furuichi, N Sakai, M Shimizu, C Segawa, K Kobayashi, N Mukaida, T Kasahara, K Matsushima and H Yokoyama
First Department of Internal Medicine and Division of Blood Purification, School of Medicine, Department of Molecular Pharmacology, Cancer Research Institute, Kanazawa University, Kanazawa, Japan; Division of Biochemistry, Kyouritsu College of Pharmacy, and Department of Molecular Preventive Medicine, University of Tokyo, Tokyo, Japan; Corresponding author at: First Department of Internal Medicine, Kanazawa University School of Medicine, 13-1 Takara-machi, Kanazawa 920-8641, Japan

Background: A potent eosinophil chemotactic cytokine, human eotaxin, is directly chemotactic for eosinophils. Therefore, the specific expression of eotaxin in tissue might play a crucial role in tissue eosinophilia. However, the precise molecular mechanism of the recruitment and activation of eosinophils in human renal diseases remains to be investigated. We evaluated the role of eotaxin in the pathogenesis of human diffuse interstitial nephritis with marked infiltration of eosinophils. Methods: In this study, we examined 20 healthy volunteers, 56 patients with primary or secondary glomerular diseases and two hypereosinophilic syndrome patients without renal involvement. Urinary and serum eotaxin levels were determined by an enzyme-linked immunosorbent assay. We also detected the presence of eotaxin protein immunohistochemically. Results: On the one hand, urinary levels of eotaxin were significantly higher before the initiation of glucocorticoid administration in the patient with interstitial nephritis with marked infiltration of eosinophils. On the other hand, urinary eotaxin levels were not detected in any patients with nephrotic syndrome, interstitial nephritis without eosinophils, hypereosinophilic syndrome without renal involvement or other renal diseases. Serum eotaxin levels were not detected in any of the patients. Therefore, the detection of eotaxin in the urine was specific for renal interstitial eosinophilia. Moreover, endothelial cells, infiltrating mononuclear cells and renal epithelial cells in the tubulointerstitial lesions were immunostained with specific anti-eotaxin antibodies. Furthermore, the elevated urinary levels of eotaxin decreased dramatically during glucocorticoid-induced convalescence. Hypothesis: We hypothesize that in situ expression of eotaxin may provide a new mechanism to explain the renal interstitial eosinophil infiltration. Key words: chemokine; eosinophilia; eotaxin; interstitium; renal disease
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