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Published on: June 8, 2022
Posttransplant tubulointerstitial nephritis: clinicopathological correlation
1Department of Pathology, Baskent University, Faculty of Medicine, Ankara, Turkey. handan27@hotmail.com
Tubulointerstitial nephritis (TIN) is a significant cause of kidney transplant dysfunction. Bacterial and viral infections leading to TIN are associated with chronic allograft nephropathy and graft loss, highlighting its pathological role.
Area of Science:
- Nephrology
- Transplantation Immunology
- Pathology
Background:
- Tubulointerstitial nephritis (TIN) is a recognized cause of renal allograft dysfunction, ranking third after rejection and cyclosporine toxicity.
- Acute TIN was identified in 8% of renal transplant biopsies, indicating its clinical relevance.
Purpose of the Study:
- To investigate the incidence, causes, and outcomes of acute tubulointerstitial nephritis in renal transplant recipients.
- To determine the association between TIN, urinary tract infections, and graft survival.
Main Methods:
- Retrospective analysis of 540 needle biopsies from 280 renal transplant patients (1996-1999).
- Identification of acute TIN and its etiologies (bacterial, cytomegalovirus, granulomatous infections).
- Correlation of TIN with rejection episodes, urinary tract infections (UTIs), chronic allograft nephropathy, and graft loss.
Main Results:
- Acute TIN was diagnosed in 23 patients (8%), primarily due to bacterial infections (17 patients) or cytomegalovirus (CMV) (3 patients).
- Urinary tract infection episodes significantly correlated with chronic allograft nephropathy (P = .03) and graft loss (P < .01).
- Graft loss occurred in 52.2% of patients within 5 years; CMV and granulomatous TIN had poorer outcomes than bacterial TIN.
Conclusions:
- Tubulointerstitial nephritis plays a significant pathological role in renal allograft deterioration and graft loss post-transplantation.
- Infections causing TIN, particularly CMV and granulomatous types, are associated with accelerated graft failure.
- Managing UTIs and identifying TIN etiologies are crucial for improving long-term renal allograft survival.
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