Literature DB >> 2675624

Immunohistochemical study of the membrane attack complex of complement and S-protein in idiopathic and secondary membranous nephropathy.

K N Lai1, S T Lo, F M Lai.   

Abstract

Twenty-eight renal biopsies from 12 patients with idiopathic membranous nephropathy (MN), eight patients with lupus MN, and eight patients with hepatitis B virus-(HBV) related MN were investigated by immunofluorescence for the presence of C5b-C9 neoantigens of the terminal sequence of complement and for S-protein, which is a regulatory component of the membrane attack complex (MAC). Glomerular MAC was detected in 50% of patients with idiopathic MN, in 75% of patients with lupus MN, and in only 12.5% of the HBsAg carrier with MN. Glomerular adhesions to Bowman's capsule were associated with a high incidence of glomerular MAC deposition only in patients with idiopathic MN. Lupus patients had a high incidence of MAC deposition and patients with HBV-related MN had a low incidence of MAC deposition, in both cases regardless of the presence of glomerular capsular adhesions. It is unlikely that deposition of S-protein could inhibit the glomerular damage in idiopathic or lupus MN because significant glomerular capsular adhesions and MAC deposition were observed despite the concomitant glomerular deposition of S-protein. It was concluded that activation of terminal components of complement may play a role in glomerular injuries in idiopathic and lupus MN. The rare occurrence of glomerular MAC deposition in HBV-related MN could be related to its distinct immunopathogenetic mechanism and its indolent clinical course.

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Year:  1989        PMID: 2675624      PMCID: PMC1879867     

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  17 in total

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Authors:  W G Couser; C K Abrass
Journal:  Annu Rev Med       Date:  1988       Impact factor: 13.739

Review 2.  Circulating DNA and lupus nephritis.

Authors:  G J Fournié
Journal:  Kidney Int       Date:  1988-02       Impact factor: 10.612

3.  In situ immune complex formation and glomerular injury.

Authors:  W G Couser; D J Salant
Journal:  Kidney Int       Date:  1980-01       Impact factor: 10.612

4.  Immunofluorescent studies on S-protein in glomeruli from patients with IgA nephropathy.

Authors:  Y Tomino; M Yagame; K Eguchi; Y Nomoto; H Sakai
Journal:  Am J Pathol       Date:  1987-11       Impact factor: 4.307

5.  Immunohistochemical study of the C5b-9 complex of complement in human kidneys.

Authors:  N Hinglais; M D Kazatchkine; S Bhakdi; M D Appay; C Mandet; J Grossetete; J Bariety
Journal:  Kidney Int       Date:  1986-09       Impact factor: 10.612

6.  The 1982 revised criteria for the classification of systemic lupus erythematosus.

Authors:  E M Tan; A S Cohen; J F Fries; A T Masi; D J McShane; N F Rothfield; J G Schaller; N Talal; R J Winchester
Journal:  Arthritis Rheum       Date:  1982-11

7.  Immunohistochemical study of the membrane attack complex of complement in IgA nephropathy.

Authors:  H Miyamoto; K Yoshioka; T Takemura; N Akano; S Maki
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1988

8.  Hepatitis B e antigen-mediated membranous glomerulonephritis. Correlation of ultrastructural changes with HBeAg in the serum and glomeruli.

Authors:  H Ito; S Hattori; I Matusda; S Amamiya; H Hajikano; H Yoshizawa; Y Miyakawa; M Mayumi
Journal:  Lab Invest       Date:  1981-03       Impact factor: 5.662

9.  IgA nephropathy associated with chronic hepatitis B virus infection in adults: the pathogenetic role of HBsAG.

Authors:  K N Lai; F M Lai; J S Tam
Journal:  J Pathol       Date:  1989-04       Impact factor: 7.996

10.  Renal localization of the membrane attack complex in systemic lupus erythematosus nephritis.

Authors:  G Biesecker; S Katz; D Koffler
Journal:  J Exp Med       Date:  1981-12-01       Impact factor: 14.307

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Review 6.  Deposition of the Membrane Attack Complex in Healthy and Diseased Human Kidneys.

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Journal:  Front Immunol       Date:  2021-02-11       Impact factor: 7.561

7.  Human kidney is a target for novel severe acute respiratory syndrome coronavirus 2 infection.

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