Prospective comparison of cytomegalovirus quantification in whole blood and plasma samples among hematopoietic stem cell transplant and kidney transplant recipients.

CMV load Cytomegalovirus HSCT Letermovir Plasma

Journal

Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology
ISSN: 1873-5967
Titre abrégé: J Clin Virol
Pays: Netherlands
ID NLM: 9815671

Informations de publication

Date de publication:
13 May 2024
Historique:
received: 15 01 2024
revised: 03 05 2024
accepted: 10 05 2024
medline: 10 6 2024
pubmed: 10 6 2024
entrez: 9 6 2024
Statut: aheadofprint

Résumé

Cytomegalovirus (CMV) induces multi-organ pathogenesis in hematopoietic stem cell transplant (HSCT) and kidney transplant (KT) recipients. Effective management involves systematic monitoring for CMV reactivation by quantitative real-time PCR, allowing timely preemptive intervention. However, the optimal blood compartment for CMV surveillance remains undetermined. The aim of the study was to compare the quantification of CMV DNA in paired plasma and whole blood samples. From June and October 2022, we conducted a prospective study with 390 sets of paired plasma and whole blood specimens collected from 60 HSCT and 24 KT recipients. CMV DNA levels were compared between the cobas® CMV assay on the automated cobas® 6800 system for plasma and the reference assay, Abbott RealTime CMV assay on the m2000 RealTime platform for whole blood. The sensitivity and specificity of CMV quantification in plasma using the cobas® CMV assay were 90.0 % (95 %CI: 81.5 to 95.9) and 94.8 % (95 %CI: 91.8 to 96.8), respectively, compared to whole blood quantification with the Abbott assay. The overall agreement between these two strategies was 0.89 (95 %CI: 0.86-0.91). In samples with quantifiable results, a correlation was observed between the two methods (R The cobas® CMV assay in plasma showed significant concordance with the Abbott RealTime CMV assay in whole blood, confirming the relevance of plasma samples for CMV monitoring in HSCT and KT recipients.

Sections du résumé

BACKGROUND BACKGROUND
Cytomegalovirus (CMV) induces multi-organ pathogenesis in hematopoietic stem cell transplant (HSCT) and kidney transplant (KT) recipients. Effective management involves systematic monitoring for CMV reactivation by quantitative real-time PCR, allowing timely preemptive intervention. However, the optimal blood compartment for CMV surveillance remains undetermined.
OBJECTIVE OBJECTIVE
The aim of the study was to compare the quantification of CMV DNA in paired plasma and whole blood samples.
STUDY DESIGN METHODS
From June and October 2022, we conducted a prospective study with 390 sets of paired plasma and whole blood specimens collected from 60 HSCT and 24 KT recipients. CMV DNA levels were compared between the cobas® CMV assay on the automated cobas® 6800 system for plasma and the reference assay, Abbott RealTime CMV assay on the m2000 RealTime platform for whole blood.
RESULTS RESULTS
The sensitivity and specificity of CMV quantification in plasma using the cobas® CMV assay were 90.0 % (95 %CI: 81.5 to 95.9) and 94.8 % (95 %CI: 91.8 to 96.8), respectively, compared to whole blood quantification with the Abbott assay. The overall agreement between these two strategies was 0.89 (95 %CI: 0.86-0.91). In samples with quantifiable results, a correlation was observed between the two methods (R
CONCLUSION CONCLUSIONS
The cobas® CMV assay in plasma showed significant concordance with the Abbott RealTime CMV assay in whole blood, confirming the relevance of plasma samples for CMV monitoring in HSCT and KT recipients.

Identifiants

pubmed: 38852538
pii: S1386-6532(24)00052-0
doi: 10.1016/j.jcv.2024.105690
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

105690

Informations de copyright

Copyright © 2024 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Linda Feghoul reports grants from Roche Diagnostics France. All other authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Marion Helary (M)

Virology Department, AP-HP, Saint Louis Hospital, F-75010 Paris, France.

Nathalie Schnepf (N)

Virology Department, AP-HP, Saint Louis Hospital, F-75010 Paris, France.

Nadia Mahjoub (N)

Virology Department, AP-HP, Saint Louis Hospital, F-75010 Paris, France.

Mathilde Lacroix (M)

Virology Department, AP-HP, Saint Louis Hospital, F-75010 Paris, France.

Alienor Xhaard (A)

Hematology Transplantation, AP-HP, Hôpital Saint Louis, F-75010 Paris, France.

Gillian Divard (G)

Kidney Transplant Department, AP-HP, Hôpital Saint Louis, F-75010 Paris, France.

Constance Delaugerre (C)

Virology Department, AP-HP, Saint Louis Hospital, F-75010 Paris, France; Université Paris Cité, INSERM U944, F-75010 Paris, France.

Lucie Biard (L)

Université Paris Cité, INSERM1153 Team ECSTRRA, Department of Biostatistics, Saint Louis Hospital, 75010 Paris, France.

Jérôme LeGoff (J)

Virology Department, AP-HP, Saint Louis Hospital, F-75010 Paris, France; Université Paris Cité, Inserm U976, Insight team, F-75010 Paris, France. Electronic address: jerome.le-goff@aphp.fr.

Linda Feghoul (L)

Virology Department, AP-HP, Saint Louis Hospital, F-75010 Paris, France.

Classifications MeSH