Literature DB >> 19696627

Expression of the decay-accelerating factor (CD55) in renal transplants--a possible prediction marker of allograft survival.

Sergey V Brodsky1, Gyongyi M Nadasdy, Ronald Pelletier, Anjali Satoskar, Daniel J Birmingham, Gregg A Hadley, Khaled Obeidat, Tibor Nadasdy.   

Abstract

BACKGROUND: Decay-accelerating factor (CD55) accelerates the decay of C3 and C5 convertases, participating in classical and alternative complement activation pathways. Complement activation plays a major role in antibody-mediated rejection of allografts (AMR); C4d is used as a marker of AMR. Emerging evidence suggests an important role of CD55 in the pathogenesis of AMR. The aim of this study was to investigate the expression of CD55 in renal allografts and to correlate it with the expression of C4d, allograft survival, changes in serum creatinine (SC).
METHODS: More than 200 renal allograft biopsies, performed for allograft dysfunction, were assessed for peritubular capillary (PTC) C4d and CD55 expression.
RESULTS: We found significant correlation between changes in SC and PTC CD55 staining pattern in patients with no PTC C4d staining. In these patients, SC increased from baseline by 2.2+0.34, 1.7+0.36, and 0.93+0.24 mg/dL in negative, focal, and diffuse PTC CD55 staining subgroups, respectively. Survival of renal allografts was better in diffuse PTC CD55 staining subgroup than in negative PTC CD55 staining subgroup.
CONCLUSIONS: These data suggest that CD55 expression has a protective effect on PTC C4d negative renal allografts, and the pattern of PTC CD55 expression may be used as a potential marker of renal allograft survival in patients with no evidence of AMR.

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Year:  2009        PMID: 19696627     DOI: 10.1097/TP.0b013e3181b0517d

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  14 in total

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Review 2.  Antibody-mediated rejection: emergence of animal models to answer clinical questions.

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Review 3.  The role of complement in antibody-mediated rejection in kidney transplantation.

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Journal:  Nat Rev Nephrol       Date:  2012-10-02       Impact factor: 28.314

Review 4.  Complement cascade and kidney transplantation: The rediscovery of an ancient enemy.

Authors:  Alberto Mella; Maria Messina; Antonio Lavacca; Luigi Biancone
Journal:  World J Transplant       Date:  2014-09-24

Review 5.  Complement involvement in kidney diseases: From physiopathology to therapeutical targeting.

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Journal:  World J Nephrol       Date:  2015-05-06

Review 6.  Complement in organ transplantation.

Authors:  Elham Asgari; Wuding Zhou; Steven Sacks
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7.  Partial dysferlin reconstitution by adult murine mesoangioblasts is sufficient for full functional recovery in a murine model of dysferlinopathy.

Authors:  J Díaz-Manera; T Touvier; A Dellavalle; R Tonlorenzi; F S Tedesco; G Messina; M Meregalli; C Navarro; L Perani; C Bonfanti; I Illa; Y Torrente; G Cossu
Journal:  Cell Death Dis       Date:  2010-08-05       Impact factor: 8.469

8.  The alternative complement pathway regulates pathological angiogenesis in the retina.

Authors:  J Harry Sweigard; Ryoji Yanai; Philipp Gaissert; Magali Saint-Geniez; Keiko Kataoka; Aristomenis Thanos; Gregory L Stahl; John D Lambris; Kip M Connor
Journal:  FASEB J       Date:  2014-03-25       Impact factor: 5.191

9.  Antibody-mediated rejection of single class I MHC-disparate cardiac allografts.

Authors:  Y Hattori; R P Bucy; Y Kubota; W M Baldwin; R L Fairchild
Journal:  Am J Transplant       Date:  2012-05-11       Impact factor: 8.086

10.  Depression of Complement Regulatory Factors in Rat and Human Renal Grafts Is Associated with the Progress of Acute T-Cell Mediated Rejection.

Authors:  Kazuaki Yamanaka; Yoichi Kakuta; Shuji Miyagawa; Shigeaki Nakazawa; Taigo Kato; Toyofumi Abe; Ryoichi Imamura; Masayoshi Okumi; Akira Maeda; Hiroomi Okuyama; Masashi Mizuno; Norio Nonomura
Journal:  PLoS One       Date:  2016-02-29       Impact factor: 3.240

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