Immunoexpression of alpha-SMA and CD68 in native kidney biopsies

Vol. 53 No. 4, 2012

ROMANIAN JOURNAL of MORPHOLOGY and EMBRYOLOGY

Ofelia Jercan, M. Penescu, D. Gh. Malaescu

Introduction: The role for inflammation and fibrosis as predictive histopathological markers for renal function has been discussed in several studies. Aim of our investigation was to evaluate the clinico-pathological correlation of myofibroblasts expression as markers for initial development of fibrotic processes and macrophagic infiltration in a population with impaired renal function, in order to better understand their value in diagnostic biopsies. Materials, Methods and Results: We evaluated 20 consecutive native kidney biopsies performed for diagnostic purposes. Material remaining after routine light microscopy and immunofluorescence, was stained for alpha-SMA as myofibroblast marker and CD68 as macrophage infiltration marker. Quantitative evaluation was conducted by electronic image analysis on consecutive low power fields, avoiding glomeruli, and estimated as percentage of the total area or as number of positive cells/field for macrophage infiltration. The renal biopsies were also evaluated for histological characteristics such as percentual area of inflammation infiltration and fibrosis. Clinical and laboratory data were recorded at biopsy moment and followed-up on a period of 17+/-11 months after the renal biopsy. Interstitial alpha-SMA immunoexpression proved to be related with interstitial fibrosis (r=-0.47, p<0.001) and macrophage infiltration (r=0.21, p=0.03). Higher immunoexpression of alpha-SMA was related with renal function assessed by creatinine level at biopsy moment (r=0.32, p=0.002). Conclusions: In this study, detection of myofibroblast infiltration using alpha-smooth-muscle actin (alpha-SMA) proved to be a good marker in describing the initial phases of interstitial fibrosis development in early stages of chronic kidney dysfunction.

Corresponding author: Ofelia Jercan, MD, PhD student; e-mail: ofeliajercan@gmail.com

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