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. 2016 Sep 29;215(1):24–33. doi: 10.1093/infdis/jiw453

Table 2.

Vaccine Response Rates at Days 30 to 360

Vaccine Formulation, Day Subjects With Response, Proportion (%) Subjects With Titer >1:1024, No. (%)
10 µg RSV-PreF
 30 9/14 (64.3) 6 (42.9)
 60 5/14 (35.7) 6 (42.9)
 180 3/14 (21.4) 2 (21.4)
 360 1/14 (7.1) 2 (14.3)
10 µg RSV-PreF/alum
 30 3/15 (20.0) 8 (53.3)
 60 5/15 (33.3) 8 (53.3)
 180 3/15 (20.0) 6 (40.0)
 360 0/14 (0.0) 2 (14.3)
30 µg RSV-PreF
 30 7/14 (50.0) 9 (64.3)
 60 6/14 (42.9) 8 (57.1)
 180 5/15 (33.3) 7 (46.7)
 360 4/15 (26.7) 6 (40.0)
30 µg RSV-PreF/alum
 30 12/14 (85.7) 12 (85.7)
 60 10/14 (71.4) 13 (92.9)
 180 6/13 (46.2) 7 (53.8)
 360 2/12 (16.7) 4 (33.3)
60 µg RSV-PreF
 30 10/15 (66.7) 11 (73.3)
 60 7/15 (46.7) 9 (60.0)
 180 3/14 (21.4) 3 (21.4)
 360 2/14 (14.3) 2 (14.3)
60 µg RSV-PreF/alum
 30 11/13 (84.6) 10 (76.9)
 60 10/14 (71.4) 7 (50.0)
 180 4/12 (33.3) 3 (25.0)
 360 3/11 (27.3) 2 (18.2)

Vaccine Response were defined as having increased by at least 4-fold from the prevaccination neutralizing antibody (nAb) titer if the prevaccination titer was <7 log2 (ie, <128), by at least 3-fold if the titer was 7–8 log2 (ie, 128–256), by at least 2.5-fold if the titer was 10 log2 (ie, 1024), and by at least 1-fold if the titer was >10 log2 (ie, >1024).

Abbreviation: RSV-PreF, respiratory syncytial virus engineered to preferentially maintain a prefusion conformation.