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Nephrol Dial Transplant (2000) 15: 1146-1154
© 2000 European Renal Association-European Dialysis and Transplant Association

Interleukin 12 induces crescentic glomerular lesions in a high IgA strain of ddY mice, independently of changes in IgA deposition

Fumiaki Nogaki1, Eri Muso1,, Ikei Kobayashi1, Hitoshi Kusano1, Kiichi Shirakawa1, Tadashi Kamata1, Atsushi Oyama1, Takahiko Ono1, Shigeki Miyawaki2, Haruyoshi Yoshida3 and Shigetake Sasayama1

1 Department of Cardiovascular Medicine, Kyoto University, Graduate School of Medicine, 2 Research Laboratories, Nippon Shinyaku Co. Ltd, Kyoto and 3 Division of Nephrology, Medical Research Institute, Kitano Hospital, Osaka, Japan

Background. Our recently established high immunoglobulin (Ig)A inbred strain (HIGA) of ddY mice showed constantly high serum IgA levels, progressive mesangial sclerosis accompanied by IgA deposits, and elevated renal expression of transforming growth factor (TGF)-ß, mimicking IgA nephropathy. In the present study, we assessed the role of the immune system, especially of T cells, in this strain.

Methods. The in vitro production of interferon (IFN)-{gamma}, interleukin (IL)-4 and TGF-ß1 by splenic CD4+ T cells was assessed in HIGA mice at 14 and 28 weeks of age by comparison with age-matched C57BL/6 and BALB/c mice, T-helper (Th) 1, and Th2 prone controls respectively. Moreover, recombinant murine IL-12 was administered intraperitoneally to HIGA mice and serum IgA and renal lesions were analysed.

Results. The production of IFN-{gamma} by splenic CD4+ T cells was markedly upregulated in HIGA mice at both ages as compared with age-matched C57BL/6 and BALB/c mice. Although splenic CD4+ T cells from HIGA mice produced less IL-4 than those from BALB/c mice at both ages, the former produced significantly more IL-4 with age, which contrasted with the age-associated decrease in the latter. Moreover, TGF-ß1 production of these cells in HIGA mice was equal to or greater than that in the two groups of control mice at both ages. Daily intraperitoneal administration of IL-12 for 1 week significantly enhanced crescent formation with glomerular macrophage accumulation and interstitial cell infiltration, whereas it reduced the serum IgA level.

Conclusions. In HIGA mice, Th1 is markedly upregulated from a young age and there is an age-associated Th2 increase with TGF-ß1 upregulation in helper T cells. The former may be related to the exacerbation of inflammatory renal lesions on IL-12 administration, while the latter may contribute to increased IgA production, leading to glomerular IgA deposition and progressive glomerulosclerosis in HIGA mice. The pathogenic role of T cell function and fluctuation of these subsets, especially the Th1/Th2 balance, is crucial to the immunopathological phenotype of the renal lesions in HIGA mice.

Keywords: crescent formation; high IgA strain of ddY mice; interleukin-12; interstitial cell infiltration; macrophages; T helper cells

Correspondence and offprint requests to: Eri Muso MD, Department of Cardiovascular Medicine, Kyoto University, Graduate School of Medicine, 54 Kawara-cho, Shogoin, Sakyo-ku, Kyoto 606–8397, Japan.


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