Low dose valganciclovir as cytomegalovirus prophylaxis in post-renal transplant recipients induced with alemtuzumab: A single-center study.


Journal

Transplant immunology
ISSN: 1878-5492
Titre abrégé: Transpl Immunol
Pays: Netherlands
ID NLM: 9309923

Informations de publication

Date de publication:
10 2019
Historique:
received: 14 05 2019
revised: 18 07 2019
accepted: 21 07 2019
pubmed: 26 7 2019
medline: 4 4 2020
entrez: 26 7 2019
Statut: ppublish

Résumé

Alemtuzumab (Ale) is a recombinant monoclonal antibody which binds to CD52 causing profound lymphodepletion, thus allowing its use in renal transplantation induction therapy. However, patients may be at increased risk for opportunistic infections, such as Cytomegalovirus (CMV). We analyzed CMV infection in renal allograft recipients administered low-dose valganciclovir (VGCV) prophylaxis with alemtuzumab induction and steroid minimization. In this retrospective analysis, 678 kidney transplant recipients were evaluated, with 606 included for analysis. Patients were excluded for receiving induction therapy other than Ale, or for lack of follow-up within 1 year. VGCV prophylaxis was stratified by recipient CMV risk status and low-dose (450 mg) VGCV was given 3 times a week to low and moderate risk patients and daily to high risk individuals. Subject records were examined for recipient demographics, donor and recipient CMV serostatus, CMV viremia, and invasive infection. Of the 606 recipients, 154 were defined as low risk for CMV infection (donor and recipient both negative, or D-/R-), 236 as moderate risk without mismatch (D+/R+), 122 as moderate risk with mismatch (D-/R+), and 94 as high risk (D+/R-). Twenty-nine (29) individuals (4.8%) tested positive by PCR for CMV viremia and 10 (1.7%) patients developed invasive CMV disease, including colitis (n = 4), esophagitis (n = 1), enteritis (n = 1), nephritis (n = 1), and pneumonia (n = 3). High risk recipients (D+/R-) accounted for the majority of invasive CMV disease (n = 5), followed by moderate risk (n = 4). CMV viremia was also more common in high risk and moderate risk (D+/R+) individuals. Overall rejection rate for our study population was 27%. In this institution's experience, CMV incidence was reduced compared to historically reported data by using low-dose (450 mg) VGCV prophylaxis in combination with Ale induction and steroid minimization. However, overall rejection rate was significantly higher in our population, possibly influenced by the degree of steroid minimization.

Identifiants

pubmed: 31344441
pii: S0966-3274(19)30067-X
doi: 10.1016/j.trim.2019.101226
pii:
doi:

Substances chimiques

Antiviral Agents 0
CD52 Antigen 0
Steroids 0
Alemtuzumab 3A189DH42V
Valganciclovir GCU97FKN3R

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

101226

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Katie Korneffel (K)

College of Medicine and Health Sciences, University of Toledo, Toledo, OH, United States of America. Electronic address: Katie.korneffel@rockets.utoledo.edu.

Graham Mitro (G)

College of Medicine and Health Sciences, University of Toledo, Toledo, OH, United States of America.

Kellie Buschor (K)

College of Pharmacy, University of Toledo, Toledo, OH, United States of America.

Michael Rees (M)

Departments of Urology and Pathology, University of Toledo College of Medicine and Health Sciences, Toledo, OH, United States of America.

Jorge Ortiz (J)

Department of Surgery, University of Toledo College of Medicine and Health Sciences, Toledo, OH, United States of America.

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Classifications MeSH