TABLE 6.
Assay and time of blood draw after seroconversiona | No. of blood specimens:
|
Sensitivity (%) by:
|
||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | With detectable CMV-specific IgG
|
Calculation method 1b | Calculation method 2b | |||||||||||
Total | Low avidity | Gray-zone avidity | High avidity | |||||||||||
Architect CMV IgG Avidity assay | ||||||||||||||
0-3 mo | 35 | 34 | 34 | 0 | 0 | 100.0 | 97.1 | |||||||
0-4 mo | 37 | 36 | 36 | 0 | 0 | 100.0 | 97.3 | |||||||
Radim CMV IgG Avidity assay | ||||||||||||||
0-3 mo | 35 | 30 | 28 | 1 | 1 | 93.3 | 80.0 | |||||||
0-4 mo | 37 | 32 | 28 | 2 | 2 | 87.5 | 75.7 | |||||||
Vidas CMV IgG Avidity assay | ||||||||||||||
0-3 mo | 35 | 31 | 5 | 26 | 0 | 16.1 | 14.3 | |||||||
0-4 mo | 37 | 33 | 5 | 28 | 0 | 15.2 | 13.5 |
All the assays tested were able to detect the early stage of seroconversion, since the validity criteria of the Architect (CMV-specific IgG concentration, ≥6.0 AU/ml), Radim (OD, >0.300), and Vidas (CMV-specific IgG concentration in the reference aliquot, ≥6 AU/ml) CMV IgG avidity assays are fulfilled.
For an explanation of the different calculation methods, see Materials and Methods.