An international collaboration to standardize HIV-2 viral load assays: Results from the 2009 ACHI EV 2E quality control study

Damond, F.;Benard, A.;Balotta, Claudia;Böni, Jürg;Brun-Vezinet, Francoise;et.al.
(2011) Journal of Clinical Microbiology — Vol. 49, n° 10, p. 3491-3497 (2011)

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Authors
  • Damond, F.
    Author
  • Benard, A.
    Author
  • Balotta, Claudia
    Author
  • Böni, Jürg
    Author
  • Ruelle, JeanUCLouvain
    Author
  • Brun-Vezinet, Francoise
    Author
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Abstract
Accurate HIV-2 plasma viral load quantification is crucial for adequate HIV-2 patient management and for the proper conduct of clinical trials and international cohort collaborations. This study compared the homogeneity of HIV-2 RNA quantification when using HIV-2 assays from ACHI <inf>E</inf>V <inf>2E</inf> study sites and either in-house PCR calibration standards or common viral load standards supplied to all collaborators. Each of the 12 participating laboratories quantified blinded HIV-2 samples, using its own HIV-2 viral load assay and standard as well as centrally validated and distributed common HIV-2 group A and B standards (http://www.hiv .lanl.gov/content/sequence/ HelpDocs/subtypes-more.html). Aliquots of HIV-2 group A and B strains, each at 2 theoretical concentrations (2.7 and 3.7 log <inf>10</inf> copies/ml), were tested. Intralaboratory, interlaboratory, and overall variances of quantification results obtained with both standards were compared using F tests. For HIV-2 group A quantifications, overall and interlaboratory and/or intralaboratory variances were significantly lower when using the common standard than when using in-house standards at the concentration levels of 2.7 log <inf>10</inf> copies/ml and 3.7 log <inf>10</inf> copies/ml, respectively. For HIV-2 group B, a high heterogeneity was observed and the variances did not differ according to the type of standard used. In this international collaboration, the use of a common standard improved the homogeneity of HIV-2 group A RNA quantification only. The diversity of HIV-2 group B, particularly in PCR primer-binding regions, may explain the heterogeneity in quantification of this strain. Development of a validated HIV-2 viral load assay that accurately quantifies distinct circulating strains is needed. Copyright © 2011, American Society for Microbiology. All Rights Reserved.
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Damond, F., Benard, A., Balotta, C., Böni, J., Cotten, M., Duque, V., Ferns, B., Garson, J., Gomes, P., Gonçalves, F., Gottlieb, G., Kupfer, B., Ruelle, J., Rodes, B., Soriano, V., Wainberg, M., Taieb, A., Matheron, S., Chene, G., & Brun-Vezinet, F. (2011). An international collaboration to standardize HIV-2 viral load assays: Results from the 2009 ACHI EV 2E quality control study. Journal of Clinical Microbiology, 49(10), 3491-3497. https://doi.org/10.1128/JCM.02389-10 (Original work published 2011)