Literature DB >> 15316375

Risk factors for capillary C4d deposition in kidney allografts: evaluation of a large study cohort.

Matthias Lorenz1, Heinz Regele, Martin Schillinger, Markus Exner, Susanne Rasoul-Rockenschaub, Markus Wahrmann, Josef Kletzmayr, Gerd Silberhumer, Walter H Hörl, Georg A Böhmig.   

Abstract

BACKGROUND: Capillary deposition of the complement split product C4d has turned out to be a valuable marker of antibody-mediated rejection. The impact of pre- and posttransplant variables including particular immunosuppressive regimens on the frequency of C4d deposition has not yet been systematically investigated in a large multivariate analysis.
METHODS: In this retrospective study, the authors evaluated the incidence of C4d deposition in 388 kidney transplant recipients subjected to diagnostic biopsy within the first 6 months and analyzed the influence of potential confounders on the rate of C4d-positive graft dysfunction by applying multivariate logistic regression.
RESULTS: Sixty-six recipients (17%) developed linear C4d deposits in at least a quarter of peritubular capillaries, a finding associated with inferior 1-year allograft survival (73% vs. 88% in C4d-negative patients, P=0.0003). A 50% reduction in the odds of C4d-positive graft dysfunction was found if calcineurin inhibitor or mycophenolate mofetil (MMF) therapy was started 2 to 4 hr before transplantation when compared with initiation after surgery (adjusted odds ratio [OR], 0.5; P=0.03). No differences with respect to C4d staining results were found for the use of tacrolimus, MMF, or sirolimus, or for cyclosporine C2 monitoring. Retransplantation (OR, 3.6; P<0.001) and presensitization (OR, 3.1; P=0.002) turned out to be strong independent risk factors for C4d deposition.
CONCLUSIONS: The authors' results suggest a reduced risk of C4d-positive graft dysfunction for patients receiving immunosuppression before transplantation. Apart from first dose timing, no influence of particular immunosuppressive strategies on C4d staining results was found.

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Year:  2004        PMID: 15316375     DOI: 10.1097/01.tp.0000128344.94808.03

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


  10 in total

1.  Critical Role of Macrophage FcγR Signaling and Reactive Oxygen Species in Alloantibody-Mediated Hepatocyte Rejection.

Authors:  Jason M Zimmerer; Xin L Liu; Alecia Blaszczak; Christina L Avila; Thomas A Pham; Robert T Warren; Ginny L Bumgardner
Journal:  J Immunol       Date:  2018-11-05       Impact factor: 5.422

2.  Critical role of effector macrophages in mediating CD4-dependent alloimmune injury of transplanted liver parenchymal cells.

Authors:  Phillip H Horne; Jason M Zimmerer; Mason G Fisher; Keri E Lunsford; Gyongyi Nadasdy; Tibor Nadasdy; Nico van Rooijen; Ginny L Bumgardner
Journal:  J Immunol       Date:  2008-07-15       Impact factor: 5.422

3.  CD8+ T cells negatively regulate IL-4-dependent, IgG1-dominant posttransplant alloantibody production.

Authors:  Jason M Zimmerer; Thomas A Pham; Virginia M Sanders; Ginny L Bumgardner
Journal:  J Immunol       Date:  2010-11-17       Impact factor: 5.422

4.  Rescue therapy with tacrolimus and mycophenolate mofetil does not prevent deterioration of graft function in C4d-positive chronic allograft nephropathy.

Authors:  Christoph Schwarz; Heinz Regele; Nicole Huttary; Markus Wahrmann; Markus Exner; Katalyn Nagy-Bojarsky; Josef Kletzmayr; Walter H Hörl; Georg A Böhmig
Journal:  Wien Klin Wochenschr       Date:  2006-07       Impact factor: 1.704

5.  C4d staining in renal allograft biopsies with early acute rejection and subsequent clinical outcome.

Authors:  Johanna M Botermans; Hanneke de Kort; Michael Eikmans; Klaas Koop; Hans J Baelde; Marko J K Mallat; Kim Zuidwijk; Cees van Kooten; Emile de Heer; Natascha N T Goemaere; Frans H J Claas; Jan A Bruijn; Johan W de Fijter; Ingeborg M Bajema; Marian C van Groningen
Journal:  Clin J Am Soc Nephrol       Date:  2011-04-28       Impact factor: 8.237

6.  Pretransplant IgG reactivity to apoptotic cells correlates with late kidney allograft loss.

Authors:  B Gao; C Moore; F Porcheray; C Rong; C Abidoglu; J DeVito; R Paine; T C Girouard; S L Saidman; D Schoenfeld; B Levin; W Wong; N Elias; C Schuetz; I Rosales; Y Fu; E Zorn
Journal:  Am J Transplant       Date:  2014-06-16       Impact factor: 8.086

7.  Focal C4d+ in renal allografts is associated with the presence of donor-specific antibodies and decreased allograft survival.

Authors:  R L Kedainis; M J Koch; D C Brennan; H Liapis
Journal:  Am J Transplant       Date:  2009-04       Impact factor: 8.086

8.  Alloprimed CD8(+) T cells regulate alloantibody and eliminate alloprimed B cells through perforin- and FasL-dependent mechanisms.

Authors:  J M Zimmerer; T A Pham; C L Wright; K J Tobin; P B Sanghavi; S M Elzein; V M Sanders; G L Bumgardner
Journal:  Am J Transplant       Date:  2014-02       Impact factor: 8.086

9.  Critical role of NKT cells in posttransplant alloantibody production.

Authors:  J M Zimmerer; P Swamy; P B Sanghavi; C L Wright; M Abdel-Rasoul; S M Elzein; R R Brutkiewicz; G L Bumgardner
Journal:  Am J Transplant       Date:  2014-09-12       Impact factor: 8.086

10.  Etiological analysis of graft dysfunction following living kidney transplantation: a report of 366 biopsies.

Authors:  Jin Zhang; Jiang Qiu; Guo-Dong Chen; Chang-Xi Wang; Chang Wang; Shuang-Jin Yu; Li-Zhong Chen
Journal:  Ren Fail       Date:  2018-11       Impact factor: 2.606

  10 in total

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