Skip to main content
. 2023 Jul 19;14:4347. doi: 10.1038/s41467-023-40057-8

Table 2.

Genotype and phenotype of major variant substitutions in the F protein of the nirsevimab binding site and changes to nirsevimab susceptibility in participants with confirmed MA RSV LRTI meeting the primary case definition in MELODY through 150 days post-dose

Amino acid substitutions Prevalence in surveillance studies (%) Placebo Nirsevimab Total Fold reduction in susceptibility IC50 (ng/mL)
Nirsevimab Palivizumab Nirsevimab Palivizumab
RSV A (n = 23) (n = 13) (n = 36)
 No change NA 23 (100%) 13 (100%) 36 (100%) 1.0 1.0 NA NA
RSV B (n = 29) (n = 10) (n = 39)
 No change NA 1 (3.4%) 0 1 (2.6%) 1.0 1.0 NA NA
 I206M:Q209R 66.0 6 (20.7%) 1 (10%) 7 (17.9%) 0.2 1.3 0.4 79.8
 I206Ma 68.9 28 (96.6%) 10 (100%) 38 (97.4%) 5 2.0 7.0 164.4
 Q209Rb 68.2 28 (96.6%) 10 (100%) 38 (97.4%) 0.5 3.1 0.9 213.7
 I206M:Q209R:S211N 1.1 22 (75.9%) 8 (80%) 30 (76.9%) 0.5 3.7 0.9 204.4
 S211Nc 1.1 22 (75.9%) 9 (90%) 31 (79.5%) 1.2 1.9 2.5 148.7
 L204S:I206M:Q209R:S211N 0 1 (10%) 1 (2.6%) ND ND ND ND
 L204Sd 0 1 (10%) 1 (2.6%) ND ND ND ND

% of participants with RSV containing substitutions in the nirsevimab binding site is calculated based on the total number of participants meeting the primary endpoint of MA RSV LRTI in each treatment arm (placebo, nirsevimab) and each RSV strain (RSV A, RSV B).

LRTI lower respiratory tract infection, MA medically attended, NA not available, ND not determined, NGS next-generation sequencing, RSV respiratory syncytial virus.

aObserved as co-occurring with Q209R ± L204S, S211N.

bObserved as co-occurring with I206M ± L204S, S211N.

cObserved only as co-occurring with I206M:Q209R.

dObserved only as co-occurring with I206M:Q209R:S211N.