TY - JOUR
T1 - S. aureus colonization in healthy Australian adults receiving an investigational S. aureus 3-antigen vaccine
AU - Marshall, Helen S.
AU - Baber, James
AU - Richmond, Peter
AU - Nissen, Michael
AU - Shakib, Sepehr
AU - Kreiswirth, Barry N.
AU - Zito, Edward T.
AU - Severs, Joseph
AU - Eiden, Joseph
AU - Gruber, William
AU - Jansen, Kathrin U.
AU - Jones, C. Hal
AU - Anderson, Annaliesa S.
PY - 2019/12
Y1 - 2019/12
N2 - Objectives: Assess Staphylococcus aureus (S. aureus) colonization in healthy Australian adults receiving an investigational S. aureus 3-antigen vaccine (SA3Ag). Methods: In this phase 1, double-blind, sponsor-unblinded study, participants were randomized to receive a single dose (1 of 3 dose levels) of SA3Ag or placebo and a booster dose or placebo at 6 months. S. aureus isolates from nasal, perineal, and oropharyngeal swabs before and through 12 months post-vaccination were identified. Results: Baseline S. aureus colonization prevalence was 30.6% (any site), with nasal carriage (27.0%) more common than oropharyngeal/perineal (3.2% each). Following initial vaccination (low-dose: 102; mid-dose: 101; high-dose: 101; placebo: 102) and booster (low-dose: 45; mid-dose: 44; high-dose: 27; placebo: 181), placebo and SA3Ag groups showed similar S. aureus carriage through 12 months. Most colonized participants (74.0%) were colonized by single spa types. Placebo and SA3Ag groups had similar persistence of colonization, with 19.6–30.7% due to single spa types. Acquisition was observed in mid- and high-dose recipients (∼20%) and low-dose and placebo recipients (∼12%). Vaccination resulted in substantial increases in antibodies to all 3 antigens, irrespective of carriage status. Conclusions: Based on descriptive analyses of this small study, SA3Ag vaccination did not impact S. aureus acquisition or carriage. Carriage status did not impact antibody responses to SA3Ag.
AB - Objectives: Assess Staphylococcus aureus (S. aureus) colonization in healthy Australian adults receiving an investigational S. aureus 3-antigen vaccine (SA3Ag). Methods: In this phase 1, double-blind, sponsor-unblinded study, participants were randomized to receive a single dose (1 of 3 dose levels) of SA3Ag or placebo and a booster dose or placebo at 6 months. S. aureus isolates from nasal, perineal, and oropharyngeal swabs before and through 12 months post-vaccination were identified. Results: Baseline S. aureus colonization prevalence was 30.6% (any site), with nasal carriage (27.0%) more common than oropharyngeal/perineal (3.2% each). Following initial vaccination (low-dose: 102; mid-dose: 101; high-dose: 101; placebo: 102) and booster (low-dose: 45; mid-dose: 44; high-dose: 27; placebo: 181), placebo and SA3Ag groups showed similar S. aureus carriage through 12 months. Most colonized participants (74.0%) were colonized by single spa types. Placebo and SA3Ag groups had similar persistence of colonization, with 19.6–30.7% due to single spa types. Acquisition was observed in mid- and high-dose recipients (∼20%) and low-dose and placebo recipients (∼12%). Vaccination resulted in substantial increases in antibodies to all 3 antigens, irrespective of carriage status. Conclusions: Based on descriptive analyses of this small study, SA3Ag vaccination did not impact S. aureus acquisition or carriage. Carriage status did not impact antibody responses to SA3Ag.
KW - Colonization
KW - Methicillin-resistant Staphylococcus aureus
KW - Spa typing
KW - Staphylococcus aureus acquisition
KW - Staphylococcus aureus vaccine
UR - http://www.scopus.com/inward/record.url?scp=85074455763&partnerID=8YFLogxK
U2 - 10.1016/j.jinf.2019.09.018
DO - 10.1016/j.jinf.2019.09.018
M3 - Article
C2 - 31585191
AN - SCOPUS:85074455763
SN - 0163-4453
VL - 79
SP - 582
EP - 592
JO - Journal of Infection
JF - Journal of Infection
IS - 6
ER -