Vimentin Expression and Myofibroblast Infiltration Are Early Markers of Renal Dysfunction in Kidney Transplantation: An Early Stage of Chronic Allograft Dysfunction?


Autoria(s): MATOS, A. C. Carvalho de; CAMARA, N. O. Saraiva; TONATO, E. J.; DURAO JR., M. de Souza; FRANCO, M. F.; MOURA, L. A. Ribeiro; PACHECO-SILVA, A.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

Introduction. The objective of this study was to show the morphologic characteristics of allograft renal biopsies in renal transplant patients with stable renal function, which can potentially be early markers of allograft dysfunction, after 5 years of follow-up. Methods. Forty-nine renal transplant patients with stable renal function were submitted to renal biopsies and simultaneous measurement of serum creatinine (Cr). Histology was evaluated using Banff scores, determination of interstitial fibrosis by Sirius red staining and immunohistochemical study of proximal tubule and interstitial compartment (using cytokeratin, vimentin, and myofibroblasts as markers). Biopsies were evaluated according to the presence or absence of the epitheliomesenchymal transition (EMT). The interstitial presence of myofibroblasts and tubular presence of vimentin was also analyzed simultaneously. Renal function was measured over the follow-up period to estimate the reduction of graft function. Results. Median posttransplant time at enrollment was 105 days. Patients were followed for 64.3 +/- 8.5 months. The mean Cr at biopsy time was 1.44 +/- 0.33 mg/dL, and after the follow-up it was 1.29 +/- 0.27 mg/dL. Nine patients (19%) had a reduction of their graft function. Eleven biopsies (22%) had tubulointerstitial alterations according to Banff score. Seventeen biopsies (34%) presented EMT. Fifteen biopsies (32%) had high interstitial expression of myofibroblasts and tubular vimentin. Using Cox multivariate analysis, HLA and high expression of interstitial myofibroblasts and tubular vimentin were associated with reduction of graft function, yielding a risk of 3.3 (P = .033) and 9.8 (P = .015), respectively. Conclusion. Fibrogenesis mechanisms occur very early after transplantation and are risk factors for long-term renal function deterioration.

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico-CNPq

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Fundacao Oswaldo Ramos

Fundacao Oswaldo Ramos

Instituto Israelita de Ensino e Pesquisa Albert Einstein, Jewish Albert Einstein Hospital, Sao Paulo, Brazil

Instituto Israelita de Ensino e Pesquisa Albert Einstein, Jewish Albert Einstein Hospital, Sao Paulo, Brazil

ROTRF

ROTRF

Identificador

TRANSPLANTATION PROCEEDINGS, v.42, n.9, p.3482-3488, 2010

0041-1345

http://producao.usp.br/handle/BDPI/28260

10.1016/j.transproceed.2010.06.014

http://dx.doi.org/10.1016/j.transproceed.2010.06.014

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE INC

Relação

Transplantation Proceedings

Direitos

restrictedAccess

Copyright ELSEVIER SCIENCE INC

Palavras-Chave #EPITHELIAL-MESENCHYMAL TRANSITION #INTERSTITIAL FIBROSIS #RISK-FACTORS #NEPHROPATHY #INJURY #REJECTION #BIOPSIES #CELLS #RATS #Immunology #Surgery #Transplantation
Tipo

article

original article

publishedVersion