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Updated: Feb 25, 2026

Trans-vivo Delayed Type Hypersensitivity Assay for Antigen Specific Regulation
Published on: May 2, 2013
AZATHIOPRINE INDUCED BONE MARROW SUPPRESSION IN LIVE RELATED RENAL ALLOGRAFT RECIPIENTS.
P P Varma1, P K Prasher1, H Madan2
1Nephrologists, Command Hospital (Southern Command), Pune.
Azathioprine can cause bone marrow suppression in kidney transplant patients. This side effect, including low blood counts, occurred in 12.9% of recipients and resolved after drug withdrawal.
Area of Science:
- Nephrology
- Immunosuppression
- Hematology
Background:
- Kidney transplantation is a vital treatment for end-stage renal disease.
- Immunosuppressive agents are crucial for preventing allograft rejection.
- Azathioprine is a commonly used immunosuppressant in organ transplantation.
Purpose of the Study:
- To investigate the incidence and clinical presentation of azathioprine-induced bone marrow suppression in live-related renal allograft recipients.
- To characterize the hematological abnormalities and recovery patterns following azathioprine withdrawal.
Main Methods:
- A retrospective analysis of 31 live-related renal allograft recipients over a 6-year follow-up period.
- Monitoring of hematological parameters, including white blood cell count, hemoglobin, and platelet count.
- Clinical assessment for adverse events and graft function.
Main Results:
- Four out of 31 recipients (12.9%) developed azathioprine-induced bone marrow suppression.
- Common presentations included leucopenia (all patients), anemia (2 patients), and pancytopenia (1 patient).
- Bone marrow suppression occurred at a median of 9.6 months post-transplant and resolved within 30 days of drug withdrawal.
Conclusions:
- Azathioprine-induced bone marrow suppression is a significant complication in renal allograft recipients.
- Early recognition and withdrawal of azathioprine are essential for patient recovery.
- Close hematological monitoring is recommended for patients receiving azathioprine post-transplantation.
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