Literature DB >> 11014582

Peritubular capillaries in chronic renal allograft rejection: a quantitative ultrastructural study.

B Iványi1, H Fahmy, H Brown, P Szenohradszky, P F Halloran, K Solez.   

Abstract

Peritubular capillaries (PCs) with a circumferentially multilayered basement membrane have been suggested as an ultrastructural indicator of chronic renal allograft rejection (CR). The authors validated this lesion as a marker for CR, by analyzing its quantitative features, specificity, and sensitivity in 169 renal biopsy specimens. The mean number of circumferential layers (PCcirc) and the incidences of the grades (mild: 2 to 4, moderate: 5 to 6, severe: 7 or more layers) were investigated in biopsy specimens involving CR (CR(Bx), n = 46), acute rejection (n = 11), normal kidneys (n = 20), psoriatics treated with cyclosporine (n = 13), renal transplants with chronic cyclosporine toxicity (n = 12), native kidney diseases (NKD, n = 56), and transplant nephrectomies attributable to CR (Cr(nephr), n = 11). CR was diagnosed with regard to the clinical features and the presence of intimal fibrosis in 41 biopsy specimens or transplant glomerulopathy in 35 biopsy specimens (cg; identified only by electron microscopy in 10 cases). NKD included chronic glomerulonephritis, chronic tubulointerstitial nephritis, benign nephrosclerosis, thrombotic microangiopathy, diabetic nephropathy, and renal disease in elderly patients (median age, 72 years). All PCs around glomeruli were sampled (median, 14 profiles per case). PCs with a moderate/ severe lesion appeared as serrated profiles with a thick, ribbon-like basement membrane layer in semithin plastic sections. The numbers of circumferentially multilayered PCs were significantly characteristic of CR (PCcirc in CR(Bx): 2.87+/-1.83 SD; range, 0 to 7.36; P < .001 v other groups). A severe lesion occurred exclusively in CR (in 12% of the PCs in CR(Bx), and in 38% in CRnephr). A moderate lesion was observed in 0.6% of the PCs in NKD, 16% in CR(Bx), and 21% in CRnephr. Three or more PCs with a moderate lesion were encountered only in CR. A mild lesion was not suggestive of CR at all. In CR(Bx), 27 cases showed a severe lesion or 3 or more PCs with a moderate lesion (cpc; sensitivity: 59%). Four of the 27 cases lacked cg. The cumulative incidence of cpc and cg was 85%. In transplants with cyclosporine toxicity, the presence of cpc verified the coexistence of CR in 7 specimens. In conclusion, cpc is a specific marker of CR. The incidence of cpc increases as CR progresses. The lesion may be caused by a low-grade rejection injury to the PCs. Careful analysis of semithin sections promotes the better sampling of cpc. An ultrastructural demonstration of cpc and cg defines CR more precisely than does light microscopic evaluation per se.

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Year:  2000        PMID: 11014582     DOI: 10.1053/hupa.2000.16677

Source DB:  PubMed          Journal:  Hum Pathol        ISSN: 0046-8177            Impact factor:   3.466


  10 in total

1.  Diminished met signaling in podocytes contributes to the development of podocytopenia in transplant glomerulopathy.

Authors:  Putri A Agustian; Mario Schiffer; Wilfried Gwinner; Irini Schäfer; Katharina Theophile; Friedrich Modde; Clemens L Bockmeyer; Jana Traeder; Ulrich Lehmann; Anika Grosshennig; Hans H Kreipe; Verena Bröcker; Jan U Becker
Journal:  Am J Pathol       Date:  2011-05       Impact factor: 4.307

Review 2.  Current pathological perspectives on chronic rejection in renal allografts.

Authors:  Shigeo Hara
Journal:  Clin Exp Nephrol       Date:  2016-11-16       Impact factor: 2.801

3.  Peritubular capillary basement membrane changes in chronic renal allograft rejection: Comparison of light microscopic and ultrastructural observations.

Authors:  Bela Ivanyi; Eva Kemeny; Peter Rago; Norbert Lazar; Krisztina Boda; Zita Morvay; Pal Szenohradszky; Edit Szederkenyi
Journal:  Virchows Arch       Date:  2011-07-01       Impact factor: 4.064

4.  Diagnostic significance of peritubular capillary basement membrane multilaminations in kidney allografts: old concepts revisited.

Authors:  George Liapis; Harsharan K Singh; Vimal K Derebail; Adil M H Gasim; Tomasz Kozlowski; Volker Nickeleit
Journal:  Transplantation       Date:  2012-09-27       Impact factor: 4.939

5.  Morphologic Features and Clinical Impact of Arteritis Concurrent with Transplant Glomerulopathy.

Authors:  Deján Dobi; Zsolt Bodó; Éva Kemény; Krisztina Boda; Pál Szenohradszky; Edit Szederkényi; Zoltan G Laszik; Béla Iványi
Journal:  Pathol Oncol Res       Date:  2015-07-23       Impact factor: 3.201

6.  Peritubular capillary basement membrane multilayering in early and advanced transplant glomerulopathy: quantitative parameters and diagnostic aspects.

Authors:  Deján Dobi; Zsolt Bodó; Éva Kemény; László Bidiga; Zoltán Hódi; Pál Szenohradszky; Edit Szederkényi; Anikó Szilvási; Béla Iványi
Journal:  Virchows Arch       Date:  2016-09-07       Impact factor: 4.064

7.  Partial therapeutic response to Rituximab for the treatment of chronic alloantibody mediated rejection of kidney allografts.

Authors:  R Neal Smith; Fahim Malik; Nelson Goes; Alton B Farris; Emmanuel Zorn; Susan Saidman; Nina Tolkoff-Rubin; Sonika Puri; Waichi Wong
Journal:  Transpl Immunol       Date:  2012-08-30       Impact factor: 1.708

Review 8.  Current status of pediatric renal transplant pathology.

Authors:  Jan U Becker
Journal:  Pediatr Nephrol       Date:  2016-05-24       Impact factor: 3.714

9.  Medullary Microvascular Thrombosis and Injury in Sickle Hemoglobin C Disease.

Authors:  Mei Lin Z Bissonnette; Kammi J Henriksen; Kristie Delaney; Nicole Stankus; Anthony Chang
Journal:  J Am Soc Nephrol       Date:  2015-11-06       Impact factor: 10.121

Review 10.  Transplant glomerulopathy.

Authors:  Edward J Filippone; Peter A McCue; John L Farber
Journal:  Mod Pathol       Date:  2017-10-13       Impact factor: 7.842

  10 in total

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