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Updated: Jun 7, 2026

Mouse Kidney Transplantation: Models of Allograft Rejection
Published on: October 11, 2014
Calcineurin inhibitor toxicity in renal allografts: morphologic clues from protocol biopsies
Alok Sharma1, Sumeet Jain, Ruchika Gupta
1Department of Pathology, All India Institute of Medical Sciences, New Delhi, India.
Background:
Calcineurin inhibitors (cyclosporine and tacrolimus) are important constituents of post renal transplant immunosuppression. However, renal toxicity limits their utility. Histological features of calcineurin inhibitor toxicity (CNIT) have been the subject of few studies using protocol biopsy samples, and consensus on diagnostic criteria is still evolving.
Aims:
To analyze the spectrum of histological changes in protocol renal allograft biopsies with evidence of CNIT and identify additional features that are likely to help the pathologist in arriving at a diagnosis.
Materials And Methods:
One hundred and forty protocol allograft biopsies performed at 1, 6 and 12 months post renal transplant were studied. The defining features of CNIT included: isometric vacuolization of proximal tubular cells, arteriolar hyalinosis with medial/peripheral nodules and striped pattern of tubular atrophy/interstitial fibrosis. Other features such as global glomerulosclerosis, vacuolization of smooth muscle cells of arterioles, tubular microcalcinosis, ischemic shrinkage of glomeruli and hyperplasia of juxtaglomerular apparatus (JGA) were also analyzed and graded semiquantitatively.
Results:
CNIT was seen in 17/140 protocol biopsies (12.1%). In addition to the diagnostic criteria, arteriolar hyalinosis, smooth muscle cell vacuolization of arterioles and hyperplasia of JGA were found to be useful indicators of CNIT.
Conclusions:
There is a relatively high incidence of CNIT in protocol allograft biopsies. A critical analysis of renal biopsy in adequate number of serial step sections to identify these features is mandatory, as many of these features are subtle and are likely to be missed if not specifically sought.
Insights
Calcineurin inhibitor toxicity (CNIT) affects 12.1% of kidney transplant patients. Pathologists should carefully examine renal biopsies for subtle signs like arteriolar hyalinosis and JGA hyperplasia to ensure accurate CNIT diagnosis.
Area of Science:
- Nephrology
- Transplant Medicine
- Pathology
Background:
- Calcineurin inhibitors (cyclosporine, tacrolimus) are vital for post-renal transplant immunosuppression.
- Renal toxicity of these inhibitors limits their clinical use.
- Diagnostic criteria for calcineurin inhibitor toxicity (CNIT) in renal allografts are still evolving.
Purpose of the Study:
- To characterize the histological changes in protocol renal allograft biopsies indicating CNIT.
- To identify additional histological features aiding CNIT diagnosis by pathologists.
Main Methods:
- Analysis of 140 protocol renal allograft biopsies at 1, 6, and 12 months post-transplant.
- Evaluation of defining CNIT features: tubular cell vacuolization, arteriolar hyalinosis, and tubular atrophy/fibrosis.
- Semiquantitative grading of additional features: glomerulosclerosis, smooth muscle cell vacuolization, microcalcinosis, glomerular ischemia, and juxtaglomerular apparatus (JGA) hyperplasia.
Main Results:
- CNIT was identified in 17 out of 140 biopsies (12.1%).
- Arteriolar hyalinosis, smooth muscle cell vacuolization, and JGA hyperplasia were significant indicators of CNIT.
- These features, alongside diagnostic criteria, aid in identifying CNIT.
Conclusions:
- CNIT exhibits a notable incidence in protocol allograft biopsies.
- Thorough examination of renal biopsies, including subtle features, is crucial for accurate CNIT diagnosis.
- Specific attention to features like arteriolar changes and JGA hyperplasia is recommended.
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