Literature DB >> 4044836

Inhibitory role of dietary protein restriction on the development and expression of immune-mediated antitubular basement membrane-induced tubulointerstitial nephritis in rats.

D Agus, R Mann, D Cohn, L Michaud, C Kelly, M Clayman, E G Neilson.   

Abstract

The protective effect of dietary protein restriction on the development and expression of immune-mediated interstitial nephritis was evaluated in Brown Norway rats with anti-tubular basement membrane disease. In the first series of experiments, pair-fed rats received low protein (LP) (3% casein) or normal protein (NP) (27% casein), normocaloric diets. After 6 wk, each group was immunized with renal tubular antigen in adjuvant to produce anti-tubular basement membrane antibody (alpha TBM-Ab) and tubulointerstitial nephritis. The kidneys harvested from NP rats after four more weeks on the diet had histologically more severe interstitial disease than the LP rats (histologic severity; NP = 3.1 +/- 0.2 vs. LP = 1.1 +/- 0.3; P less than 0.001), and serum creatinine values were concordantly different (NP = 1.34 +/- 0.02 vs. LP = 0.82 +/- 0.03). Titers of alpha TBM-Ab were similar in both groups, while the T cell-mediated immune response, as measured by delayed-type hypersensitivity (DTH), was nonspecifically impaired in LP rats when compared with the NP group. Admixture cotransfers of LP plus NP cells failed to demonstrate active suppression as an explanation for the depressed DTH in LP rats. The therapeutic role of dietary protein restriction was also examined in rats with established alpha TBM disease. In these experiments, rats were first immunized and fed NP diets for 4 wk (histologic severity = 3.0 +/- 0.2; creatinine = 1.78 +/- 0.02), and then were divided into two groups and followed for six more weeks on either LP or NP diets. LP rats, under these conditions, developed less disease than those fed NP diet (histologic severity; NP = 3.2 +/- 0.3 vs. LP = 1.4 +/- 0.2; P less than 0.001), and serum creatinine values were concordantly different (NP = 1.92 +/- 0.05 vs. LP = 0.97 +/- 0.02). Again, the titers of alpha TBM-Ab in both LP and NP groups were similar. These data collectively suggest that LP diet has a protective effect both on the development and extent of tubulointerstitial nephritis that is perhaps, in part, related to the selective abrogation of effector T cell immunity.

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Year:  1985        PMID: 4044836      PMCID: PMC423956          DOI: 10.1172/JCI112092

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  29 in total

1.  The distribution and initial characterization of oligosaccharide units on the COOH-terminal propeptide extensions of the pro-alpha 1 and pro-alpha 2 chains of type I procollagen.

Authors:  C C Clark
Journal:  J Biol Chem       Date:  1979-11-10       Impact factor: 5.157

2.  Influence of dietary restriction on immunologic function and renal disease in (NZB x NZW) F1 mice.

Authors:  G Fernandes; P Friend; E J Yunis; R A Good
Journal:  Proc Natl Acad Sci U S A       Date:  1978-03       Impact factor: 11.205

3.  Cell-mediated immunity in interstitial nephritis. I. T lymphocyte systems in nephritic guinea pigs: the natural history and diversity of the immune response.

Authors:  E G Neilson; S M Phillips
Journal:  J Immunol       Date:  1979-11       Impact factor: 5.422

4.  Polymorphism of genes involved in anti-tubular basement membrane disease in rats.

Authors:  E G Neilson; D L Gasser; E McCafferty; B Zakheim; S M Phillips
Journal:  Immunogenetics       Date:  1983       Impact factor: 2.846

5.  Nutritional modulation of immune responses.

Authors:  R A Good; A West; G Fernandes
Journal:  Fed Proc       Date:  1980-11

Review 6.  Dietary protein intake and the progressive nature of kidney disease: the role of hemodynamically mediated glomerular injury in the pathogenesis of progressive glomerular sclerosis in aging, renal ablation, and intrinsic renal disease.

Authors:  B M Brenner; T W Meyer; T H Hostetter
Journal:  N Engl J Med       Date:  1982-09-09       Impact factor: 91.245

7.  Preservation of function in experimental renal disease by dietary restriction of phosphate.

Authors:  L S Ibels; A C Alfrey; L Haut; W E Huffer
Journal:  N Engl J Med       Date:  1978-01-19       Impact factor: 91.245

8.  The role of the interstitium of the renal cortex in renal disease.

Authors:  A Bohle; H Christ; K E Grund; S Mackensen
Journal:  Contrib Nephrol       Date:  1979       Impact factor: 1.580

9.  Suppression of interstitial nephritis by auto-anti-idiotypic immunity.

Authors:  E G Neilson; M Phillips
Journal:  J Exp Med       Date:  1982-01-01       Impact factor: 14.307

10.  Murine interstitial nephritis. I. Analysis of disease susceptibility and its relationship of pleiomorphic gene products defining both immune-response genes and a restrictive requirement for cytotoxic T cells at H-2K.

Authors:  E G Neilson; S M Phillips
Journal:  J Exp Med       Date:  1982-04-01       Impact factor: 14.307

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  2 in total

1.  Irreversible tubulointerstitial damage associated with chronic aminonucleoside nephrosis. Amelioration by angiotensin I converting enzyme inhibition.

Authors:  J R Diamond; S Anderson
Journal:  Am J Pathol       Date:  1990-12       Impact factor: 4.307

2.  Prostaglandin E1 inhibits effector T cell induction and tissue damage in experimental murine interstitial nephritis.

Authors:  C J Kelly; R B Zurier; K A Krakauer; N Blanchard; E G Neilson
Journal:  J Clin Invest       Date:  1987-03       Impact factor: 14.808

  2 in total

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