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Mycophenolate mofetil may protect against Pneumocystis carinii pneumonia in renal transplanted patients
Luiz Sergio Azevedo1, Maria Cristina R Castro, Flavio J Paula
1Renal Transplantation Unit, Hospital das Clínicas, Medical School, University of São Paulo, São Paulo, SP, Brazil. ls.azevedo@terra.com.br
Abstract:
Pneumocystis carinii pneumonia (PCP) is usually prevented in transplanted patients by prophylactic trimethoprim-sulfamethoxazol (TMS). Mycophenolate mofetil (MMF) has been shown to have a strong protective effect against PCP in rats. This effect is also suggested in humans by the absence of PCP in patients receiving MMF. After January 1998 MMF has been used with no TMS prophylaxis in renal transplanted patients. In azathioprine (AZA) treated patients TMS prophylaxis was maintained. The incidence of PCP was analyzed in both groups. Data were collected in order to have a minimum 6-month follow-up. Two hundred and seventy-two patients were eligible for analysis. No PCP occurred either in patients under MMF without TMS prophylaxis nor in patients under AZA. MMF may have an effective protective role against PCP as no patient under MMF, despite not receiving TMS coverage, developed PCP. A larger, controlled, trial is warranted to consolidate this information.
Insights
Mycophenolate mofetil (MMF) may prevent Pneumocystis pneumonia (PCP) in transplant patients without trimethoprim-sulfamethoxazole (TMS) prophylaxis. No PCP cases occurred in MMF or azathioprine groups, suggesting MMF
Area of Science:
- Nephrology
- Infectious Disease
- Immunosuppression
Background:
- Pneumocystis carinii pneumonia (PCP) is a significant opportunistic infection in transplant recipients.
- Trimethoprim-sulfamethoxazole (TMS) is the standard prophylactic agent against PCP.
- Mycophenolate mofetil (MMF) has demonstrated potential anti-PCP properties in preclinical studies.
Purpose of the Study:
- To evaluate the efficacy of MMF in preventing PCP in renal transplant patients.
- To compare PCP incidence in MMF-treated patients (without TMS) versus azathioprine (AZA)-treated patients (with TMS).
Main Methods:
- Retrospective analysis of 272 renal transplant patients with a minimum 6-month follow-up.
- Patients were divided into two groups: MMF without TMS prophylaxis and AZA with TMS prophylaxis.
- Incidence of PCP was the primary outcome measure.
Main Results:
- No cases of PCP were observed in either the MMF group (without TMS) or the AZA group (with TMS).
- This suggests MMF may offer protection against PCP even without concurrent TMS prophylaxis.
Conclusions:
- MMF may possess intrinsic anti-PCP activity in renal transplant recipients.
- Further large-scale, controlled trials are necessary to confirm the prophylactic role of MMF against PCP.
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