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Leishmaniasis in transplant patients: what do we know so far?
Begoña Monge-Maillo1, Rogelio López-Vélez
1National Reference Unit for Tropical Diseases, WHO Collaborating Centre for Clinical Management of Leishmaniasis, Infectious Diseases Department, Ramón y Cajal University Hospital, IRICYS. CIBERINFEC, Madrid, Spain.
Current Opinion in Infectious Diseases
|July 16, 2024
Summary
Transplant patients with visceral leishmaniasis, often linked to immunosuppression, require updated management. New biomarkers may help monitor treatment effectiveness and guide secondary prophylaxis in these growing cases.
Area of Science:
- * Infectious Diseases
- * Immunology
- * Transplantation
Background:
- * Visceral leishmaniasis (VL) cases in immunosuppressed non-HIV patients, particularly kidney transplant recipients, are increasing.
- * Transplant-associated immunosuppression is a significant risk factor for VL development and recurrence.
Purpose of the Study:
- * To review and update the latest developments in the diagnostic management, treatment, and follow-up of visceral leishmaniasis in transplant recipients.
- * To highlight the growing challenge of VL in the context of organ transplantation and immunosuppression.
Main Methods:
- * Comprehensive literature review of recent studies on visceral leishmaniasis in transplant recipients.
- * Analysis of current treatment guidelines and emerging diagnostic and prognostic markers.
Main Results:
- * Liposomal amphotericin B is the established first-line treatment for VL in transplant patients.
- * Recurrent infections are common due to ongoing immunosuppression.
- * Cellular immune response markers post-treatment show promise as biomarkers for cure, monitoring, and guiding secondary prophylaxis.
Conclusions:
- * There is a lack of consensus on donor/recipient screening protocols and indications for secondary prophylaxis.
- * Further research into novel biomarkers for cure assessment is crucial for managing VL in transplant recipients.
- * Biomarkers could aid in treatment monitoring and prophylaxis decisions in this vulnerable population.
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