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Objectives: Cytomegalovirus infection is the most common opportunistic infection affecting organ transplant recipients and is associated with detrimental allograft and patient outcomes. In recipients previously seronegative for cytomegalovirus, acquired infection is termed primary infection, whereas infection acquired in recipients with previously confirmed seropositivity is called reactivation. Cytomegalovirus seropositivity carries a great risk of reactivation, and management for these patients may vary, from dug prophylaxis to pre emptive viral monitoring.We soughtto determine the incidence of cytomegalovirus reactivation in kidney recipients with cytomegalovirus seropositivity and to assess risk factors.
Materials And Methods: We conducted a retrospective study at our center to determine the overall incidence of cytomegalovirus reactivation and associated risk factors in kidney transplant recipients with cytomegalovirus seropositivity within 12 months of transplant. For the period January 2015 to January 2021, we studied 97 transplant recipients who were seropositive for cytomegalovirus.
Results: Cytomegalovirus reactivation developed in 49 of 97 recipients (50.5%); cytomegalovirus reactivation developed in 63% of recipients ≥65 years versus 42% <65 years (P = .046); and 76% of cytomegalovirus reactivations occurred within the first 3 months after transplant (P <.001). Mean glomerular filtration rate at 12 months was significantly lower in patients with cytomegalovirus reactivation (37.86 mL/min) versus without reactivation (50.85 mL/min; P = .005). Binary logistic regression analysis revealed recipient age ≥65 years as a predictor of cytomegalovirus reactivation on univariate analysis.
Conclusions: Kidney transplant recipients ≥65 years were more likely to develop cytomegalovirus reactivation in the first 3 to 6 months posttransplant. Kidney allograft function at 12 months was significantly lower in recipients with cytomegalovirus reactivation. Our results suggest that universal cytomegalovirus drug prophylaxis in kidney recipients with cytomegalovirus seropositivity may help reduce cytomegalovirus reactivation and prevent associated adverse outcomes in older kidney transplant recipients.
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http://dx.doi.org/10.6002/ect.2024.0194 | DOI Listing |
Front Immunol
September 2025
School of Medicine, Nankai University, Tianjin, China.
Purpose: Relapse remains the leading cause of treatment failure in high-risk acute myeloid leukemia (AML) or myelodysplastic syndrome-IB (MDS-IB) patients after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Ruxolitinib has demonstrated antileukemic activity , and decitabine has been found to be tolerable when combined with modified busulfan-cyclophosphamide (mBu/Cy) conditioning regimen. Here, we investigated the efficacy of ruxolitinib and decitabine plus a mBu/Cy conditioning regimen (Rux-Dec-mBu/Cy) in reducing relapse in high-risk AML/MDS patients ().
View Article and Find Full Text PDFClin Mol Hepatol
September 2025
European Foundation for Study of Chronic Liver Failure, EF-Clif, Barcelona, Spain.
Viruses
July 2025
Faculty of Medicine, The Hashemite University, Zarqa 13133, Jordan.
Background: Cytomegalovirus (CMV) colitis is commonly seen in patients who are immunodeficient or have inflammatory bowel disease. Among the gastrointestinal sites affected by CMV, the colon is the most frequently affected, though rectal involvement is relatively rare. Reactivated CMV proctitis primarily occurs in elderly patients with comorbidities and is quite uncommon in immunocompetent individuals.
View Article and Find Full Text PDFClin Microbiol Infect
August 2025
Department of Infectious Diseases, Infection Control and Employee Health, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Objectives: Epstein-Barr virus (EBV) reactivation following allogeneic hematopoietic cell transplantation (allo-HCT) is associated with increased mortality and possible post-transplant lymphoproliferative disorder (PTLD). With the lack of prophylactic agents, identifying modifiable risk factors to prevent EBV-related mortality is desired. Cytomegalovirus (CMV) DNAemia has been previously associated with EBV DNAemia; the impact of letermovir prophylaxis on this association remains unclear.
View Article and Find Full Text PDFJ Virol
August 2025
Infection Biology, Sheikha Fatima bint Mubarak Global Center for Pathogen and Human Health Research, Cleveland Clinic Research, Cleveland Clinic, Cleveland, Ohio, USA.
Human cytomegalovirus (CMV) is a ubiquitous pathogen that establishes lifelong, latent infection in hematopoietic cells. Immune-competent individuals are usually asymptomatic for disease. However, immune dysregulation in latently infected individuals can result in viral reactivation, often causing further complications.
View Article and Find Full Text PDF