Literature DB >> 2955967

Relationship of the quality and quantity of circulating anti-BSA antibodies to the severity of glomerulonephritis in rats with chronic serum sickness.

B Noble, M W Steward, A Vladutiu, J R Brentjens.   

Abstract

Chronic serum sickness glomerulonephritis, induced in hyperimmunized rats by daily intravenous administration of bovine serum albumin, occurs in three stages, mild, moderate and severe, with abrupt onsets and distinctive features of kidney pathophysiology and immunopathology. We have studied the relationship between circulating anti-BSA antibodies and the severity of glomerulonephritis at each stage. The total amount of antibodies declined gradually during the course of disease, to low concentrations in the most severe stage of kidney inflammation. High levels of immune complexes were present in the circulation while precipitating antibodies were maintained, and rats remained in the mill stage of disease, exhibiting no abnormalities of kidney function and only mesangial immunopathology. The start of the moderate stage of chronic serum sickness, identified by proteinuria and the accumulation of immune deposits along the glomerular basement membrane, was associated with the disappearance of precipitating antibodies from circulation. With the onset of the severe stage of disease, marked by depressed glomerular filtration and sodium excretion, circulating antibodies of high affinity were no longer detected and circulating immune complex levels were only marginally elevated above normal. The experiments reported here demonstrate that, in chronic serum sickness glomerulonephritis of rats, transitions from one stage of kidney disease to another can be inferred from changes in the population of circulating antibodies. Kidney histopathology, therefore, can be predicted reliably from serological data alone.

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Year:  1987        PMID: 2955967      PMCID: PMC1542590     

Source DB:  PubMed          Journal:  Clin Exp Immunol        ISSN: 0009-9104            Impact factor:   4.330


  20 in total

1.  Experimental chronic serum sickness in rabbits that received daily multiple and high doses of antigen: a systemic disease.

Authors:  J R Brentjens; D W O'Connell; B Albini; G A Andres
Journal:  Ann N Y Acad Sci       Date:  1975-06-30       Impact factor: 5.691

2.  A method of trace iodination of proteins for immunologic studies.

Authors:  P J McConahey; F J Dixon
Journal:  Int Arch Allergy Appl Immunol       Date:  1966

3.  The use of a double isotope method in the determination of antibody affinity.

Authors:  S Gaze; N J West; M W Steward
Journal:  J Immunol Methods       Date:  1973-12       Impact factor: 2.303

4.  Precipitating antibody to D.N.A. detected by two-stage electroimmunodiffusion. Study in S.L.E. and in rheumatoid arthritis.

Authors:  G D Johnson; J P Edmonds; E J Holborow
Journal:  Lancet       Date:  1973-10-20       Impact factor: 79.321

5.  The effect of cyclophosphamide on the antibody response.

Authors:  M W Steward; J H Alpers; J F Soothill
Journal:  Proc R Soc Med       Date:  1973-08

6.  Chronic glomerulonephritis induced by prolonged immunization in the rabbit.

Authors:  T Kuriyama
Journal:  Lab Invest       Date:  1973-02       Impact factor: 5.662

7.  The immunopathological significance of the heterogeneity of antibody affinity.

Authors:  J F Soothill; M W Steward
Journal:  Clin Exp Immunol       Date:  1971-08       Impact factor: 4.330

8.  The Raji cell radioimmune assay for detecting immune complexes in human sera.

Authors:  A N Theofilopoulos; C B Wilson; F J Dixon
Journal:  J Clin Invest       Date:  1976-01       Impact factor: 14.808

9.  Dietary fat and immune function. II. Effects on immune complex nephritis in (NZB x NZW)F1 mice.

Authors:  W Yumura; S Hattori; W J Morrow; D C Mayes; J A Levy; T Shirai
Journal:  J Immunol       Date:  1985-12       Impact factor: 5.422

10.  Experimental immune complex disease of the lung. The pathogenesis of a laboratory model resembling certain human interstitial lung diseases.

Authors:  J R Brentjens; D W O'Connell; I B Pawlowski; K C Hsu; G A Andres
Journal:  J Exp Med       Date:  1974-07-01       Impact factor: 14.307

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  2 in total

1.  Capillary-localized low-affinity antibody-antigen complexes act as a focus for the deposition of high-affinity complexes.

Authors:  K Moulder; M W Steward
Journal:  Clin Exp Immunol       Date:  1989-08       Impact factor: 4.330

2.  Effect of cyclosporin on immune complex deposition in murine glomerulonephritis.

Authors:  D G Quinn; J S Fennell; O Sheils; E F Gaffney; C F Feighery
Journal:  Immunology       Date:  1991-04       Impact factor: 7.397

  2 in total

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