BackgroundOptimal care of persons infected with human immunodeficiency virus type 2 (HIV-2) requires an accurate assessment of HIV-2 plasma viral load (VL), but no clinically approved quantitative HIV-2 RNA VL assay exists. ObjectivesTo validate a novel quantitative HIV-2 RNA assay for clinical and research use. Study designThe Abbott m2000sp/rt platform was adapted for quantification of HIV-2 RNA in plasma. Amplification targeted a region of the long terminal repeat conserved in Group A and B HIV-2. Electron microscopy-counted-HIV-2 standards, the WHO/NIBSC HIV-2 International Standard and clinical specimens (N=162) were used to determine the precision, sensitivity, specificity, linear range, accuracy, and clinical performance of the assay. ResultsThe quantitative linear range of the HIV-2 RNA assay was 10–1,000,000copies/mL (R2>0.99), with a limit of detection of 8copies/mL (95% CI, 5–18copies/mL). The assay did not cross-react with HIV-1, and quantification of HIV-2 RNA was not affected by the presence of >5log10HIV-1RNAcopies/mL. The total standard deviation (SD) and intra- and inter-run SD were 0.095, 0.093 and 0.162, respectively, at nominal inputs of 3.7, 1.7 and 1.0log10HIV-2RNAcopies/mL. The HIV-2 WHO/NIBSC International Standard (1000IU) was shown to contain 152RNAcopies/mL (95% CI 141–163). Overall, HIV-2 RNA was quantified at ≥10copies/mL from 86 (53%) clinical specimens (median, 2.24log10copies/mL; range 10–16,870), and nine specimens (6%) had HIV-2 RNA detected at <10copies/mL. ConclusionsWe developed and validated a highly sensitive HIV-2 VL assay that is suitable for clinical and research use.