An international multi-site study to evaluate the analytical and clinical performance of the quantitative high-throughput Alinity m CMV assay

Cytomegalovirus (CMV) has a high prevalence in the general population and lifelong latency once an individual is infected. Primary infection or reactivation of CMV in immunocompromised individuals can lead to serious illness, organ failure, and death. Precise and accurate quantification of CMV is a valuable tool to support clinical decision-making and prevent adverse outcomes in transplant recipients. This international multicenter study evaluated the analytical performance of the Alinity m CMV assay using a commercially available panel (2.30 to 6.60 Log IU/mL) and clinical performance compared to the Abbott RealTi<i>m</i>e CMV assay and Roche cobas CMV assay run on the cobas 6800 system using deidentified remnant plasma specimens. Analysis of analytical precision with the commercial panel revealed a %CV of ≤6.6% and a total SD of ≤0.18 Log IU/mL. Plasma specimens (<i>n</i> = 748) initially tested with the RealTi<i>m</i>e CMV assay and subsequently run on the Alinity m CMV assay demonstrated a correlation coefficient of 0.972 with a mean bias of -0.05 Log IU/mL. Comparison of the Alinity m CMV and cobas CMV assays utilizing a separate set of plasma specimens (<i>n</i> = 303) demonstrated a correlation coefficient of 0.979 with a mean bias of 0.09 Log IU/mL. The overall percent agreement between Alinity m CMV and RealTi<i>m</i>e CMV assay results and between Alinity m CMV and cobas CMV assay results at clinically relevant thresholds was ≥95.7% and ≥96.4%, respectively. The high precision, accuracy, and comparable clinical performance of the Alinity m CMV assay, combined with rapid results reporting, support its use in transplant patient management.IMPORTANCECytomegalovirus (CMV) in transplant patients can lead to adverse health consequences. Viral load monitoring is important in post-transplant patient care. Clinical diagnostic laboratories utilize various molecular diagnostic platforms. This study evaluated the Alinity m CMV assay with two commercially available assays: the Abbott RealTime CMV and Roche cobas CMV assays. Our results demonstrated a strong correlation between Alinity m CMV and the comparator assays, ensuring comparable results across these platforms.

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Publication Details

Journal
Microbiology Spectrum
Published
2025-08-19
DOI
https://doi.org/10.1128/spectrum.02009-24
Primary Topic
Cytomegalovirus and herpesvirus research
Type
article
Field-Weighted Citation Impact
0.00
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article

An international multi-site study to evaluate the analytical and clinical performance of the quantitative high-throughput Alinity m CMV assay

Patricia Jim, Tianxi Liu, Tanjina Akter, Yan‐Chin Tai et al.
Microbiology Spectrum
Cytomegalovirus and herpesvirus research
article

An international multi-site study to evaluate the analytical and clinical performance of the quantitative high-throughput Alinity m CMV assay

Patricia Jim, Tianxi Liu, Tanjina Akter, Yan‐Chin Tai, Julie Hirschhorn, Ya-Jhu Lin, Momka Narlieva, Danijela Lucic, Tanisha Dickerson, April Kegl, Jen‐Fu Hsu, Tzu-Hsuan Hsieh, D. Goldstein, Lian Wu, Stephen Young, Po-Wei Huang, Mark M. Sasaki, Eriel Thornton, Nhi Nhan, Chung‐Guei Huang
article en

Abstract

Cytomegalovirus (CMV) has a high prevalence in the general population and lifelong latency once an individual is infected. Primary infection or reactivation of CMV in immunocompromised individuals can lead to serious illness, organ failure, and death. Precise and accurate quantification of CMV is a valuable tool to support clinical decision-making and prevent adverse outcomes in transplant recipients. This international multicenter study evaluated the analytical performance of the Alinity m CMV assay using a commercially available panel (2.30 to 6.60 Log IU/mL) and clinical performance compared to the Abbott RealTi<i>m</i>e CMV assay and Roche cobas CMV assay run on the cobas 6800 system using deidentified remnant plasma specimens. Analysis of analytical precision with the commercial panel revealed a %CV of ≤6.6% and a total SD of ≤0.18 Log IU/mL. Plasma specimens (<i>n</i> = 748) initially tested with the RealTi<i>m</i>e CMV assay and subsequently run on the Alinity m CMV assay demonstrated a correlation coefficient of 0.972 with a mean bias of -0.05 Log IU/mL. Comparison of the Alinity m CMV and cobas CMV assays utilizing a separate set of plasma specimens (<i>n</i> = 303) demonstrated a correlation coefficient of 0.979 with a mean bias of 0.09 Log IU/mL. The overall percent agreement between Alinity m CMV and RealTi<i>m</i>e CMV assay results and between Alinity m CMV and cobas CMV assay results at clinically relevant thresholds was ≥95.7% and ≥96.4%, respectively. The high precision, accuracy, and comparable clinical performance of the Alinity m CMV assay, combined with rapid results reporting, support its use in transplant patient management.IMPORTANCECytomegalovirus (CMV) in transplant patients can lead to adverse health consequences. Viral load monitoring is important in post-transplant patient care. Clinical diagnostic laboratories utilize various molecular diagnostic platforms. This study evaluated the Alinity m CMV assay with two commercially available assays: the Abbott RealTime CMV and Roche cobas CMV assays. Our results demonstrated a strong correlation between Alinity m CMV and the comparator assays, ensuring comparable results across these platforms.

Microbiology SpectrumVol. 13(10)
Montefiore Medical Center (US), Chang Gung University of Science and Technology (TW), Medical University of South Carolina (US), Chang Gung University (TW), National Tsing Hua University (TW), Abbott (United Kingdom) (GB), Chang Gung Memorial Hospital (TW), Abbott (United States) (US), Abbott (Singapore) (SG), Linkou Chang Gung Memorial Hospital (TW), Abbott Fund (US), Applied Research Associates (United States) (US), Ekaterinburg Research Institute of Viral Infections (RU)
Openalex Percentile: Top 71%
Cytomegalovirus and herpesvirus research
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