Skip to main content
. 2021 May 19;59(6):e03161-20. doi: 10.1128/JCM.03161-20

TABLE 4.

Results and calculated specificities of the commercial methods for the detection of anti-measles IgM antibodies evaluated with the non-measles sera panel (n = 187), by subseta

Method No. of positive or equivocal results (specificity, %)
95% CI of specificity
Chikungunya (n = 4) Dengue (n = 34) Parvovirus B19 (n = 35) Roseola (n = 38) Rubella (n = 36) Zika (n = 3) Unknownb (n = 37) Total (n = 187)
Enzygnost 0 (100) 0 (100) 7 (80.0) 2 (94.7) 0 (100) 0 (100) 0 (100) 9 (95.2) 90.8–97.6
Euroimmun 1 (75) 0 (100) 6 (82.9) 1 (97.4) 0 (100) 0 (100) 0 (100) 8 (95.7) 91.4–98.0
Euroimmun Nucleoprotein 0 (100) 0 (100) 1 (97.1) 0 (100) 0 (100) 0 (100) 1 (97.3) 2 (98.9) 95.8–99.8
IBL 0 (100) 2 (94.1) 0 (100) 0 (100) 3 (91.7) 1 (66.7) 1 (97.3) 7 (96.3) 92.1–98.3
LIAISON XL 0 (100) 0 (100) 1 (97.1) 0 (100) 0 (100) 0 (100) 0 (100) 1 (99.5d) 96.6–100
Microimmune 0 (100) 1 (97.1) 0 (100) 2 (94.7) 0 (100) 1 (66.7) 1 (97.3) 5 (97.3) 93.5–99.0
NovaLisa 0 (100) 2 (94.1) 15 (57.1) 2 (94.7) 0 (100) 1 (66.7) 1 (97.3) 21 (88.8d) 83.1–92.8
Serion (activity calculator)c 0 (100) 0 (100) 16 (54.3) 2 (94.7) 0 (100) 2 (33.3) 1 (97.3) 21 (88.8d) 83.1–92.8
Serion (OD range)c 0 (100) 0 (100) 15 (57.1) 2 (94.7) 0 (100) 2 (33.3) 1 (97.3) 20 (89.3d) 83.7–93.2
Serion (special case formula)c 1 (75) 0 (100) 17 (51.4) 3 (92.1) 0 (100) 2 (33.3) 2 (94.6) 25 (86.6d) 80.7–91.0
a

Specimens with equivocal results were counted as positive.

b

This panel of sera included fever/rash illness of unknown etiology.

c

Three methods of sample result determination, using the single set of optical density data from the test plates, were provided in the manufacturer’s IFU. All three methods were evaluated.

d

Significant difference (P < 0.05) between the most specific (LIAISON XL) and the least specific methods (Serion, all three result determination methods, and NovaLisa) based on nonoverlapping 95% confidence intervals.