Five-year Antibody Persistence and Booster Response to a Single Dose of Meningococcal A, C, W and Y Tetanus Toxoid Conjugate Vaccine in Adolescents and Young Adults An Open, Randomized Trial

被引:31
作者
Baxter, Roger [1 ]
Baine, Yaela [2 ,3 ]
Kolhe, Devayani
Baccarini, Carmen I. [2 ,3 ]
Miller, Jacqueline M. [2 ,3 ]
Van der Wielen, Marie [4 ]
机构
[1] Kaiser Permanente Vaccine Study Ctr, Oakland, CA 94612 USA
[2] GSK Vaccines, Vaccine Discovery & Dev, King Of Prussia, PA USA
[3] GSK Pharmaceut India Ltd, Pharma Europe & EMAP, Bangalore, Karnataka, India
[4] GSK Vaccines, Clin R&D, Wavre, Belgium
关键词
quadrivalent meningococcal vaccine; conjugate vaccine; antibody persistence; booster response; adolescents; ADVISORY-COMMITTEE; W-135; IMMUNOGENICITY; SEROGROUPS; SAFETY; DISEASE; IMMUNIZATION; PREVENTION; RECOMMENDATIONS; PROFILE;
D O I
10.1097/INF.0000000000000866
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: We evaluated antibody persistence after 1 dose of meningococcal serogroups ACWY tetanus toxoid (MenACWY-TT) or diphtheria toxoid (MenACWY-DT) conjugate vaccines and subsequent booster responses to MenACWY-TT. Methods: In the initial phase II, open, multicenter study (NCT00454909), 872 participants aged 10-25 years received 1 MenACWY-TT or MenACWY-DT dose. In this study (NCT00715910), antibody persistence was evaluated at years 1, 3 and 5 by serum bactericidal activity assays using human complement (hSBA). At year 5, all participants received a MenACWY-TT booster dose. Immune responses at 1-month postbooster were compared with a control group including 101 participants aged 15-30 years who received a primary MenACWY-TT dose. Solicited and unsolicited adverse events were recorded for 4 and 31 days, respectively, followed by a 6-month extended safety follow-up. Results: At year 5, 79.5% of MenACWY-TT-primed (n = 170) and MenACWY-DT-primed (n = 45) participants had hSBA titers 1:8 for MenC, MenW and MenY, and 37.5% for MenA. For all serogroups, 85.7% and 67.1% of MenACWY-TT booster and primary dose recipients exhibited vaccine responses 1-month postmvaccination, respectively. Geometric mean titers were potentially higher in primed versus naive participants, with no potential difference between MenACWY-TT-primed and MenACWY-DT-primed participants (exploratory analyses). MenACWY-TT had a clinically acceptable safety profile. Conclusions: Before the booster dose administration at year 5, hSBA-MenC, -MenW and -MenY antibody persistence was observed in most participants. However, only 37.5% of MenACWY-TT and 44.4% of MenACWY-DT recipients retained hSBA-MenA titers 1:8. MenACWY-TT booster doses elicited robust anamnestic responses, irrespective of the priming vaccine, and were well tolerated.
引用
收藏
页码:1236 / 1243
页数:8
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