A Phase 2, Randomized, Control Trial of Group B Streptococcus (GBS) Type III Capsular Polysaccharide-tetanus Toxoid (GBS III-TT) Vaccine to Prevent Vaginal Colonization With GBS III

被引:35
|
作者
Hillier, Sharon L. [1 ]
Ferrieri, Patricia [2 ]
Edwards, Morven S. [3 ]
Ewell, Marian [4 ]
Ferris, Daron [5 ]
Fine, Paul [6 ]
Carey, Vincent [7 ,8 ]
Meyn, Leslie [1 ]
Hoagland, Dakota [9 ]
Kasper, Dennis L. [10 ]
Paoletti, Lawrence C. [10 ]
Hill, Heather [4 ]
Baker, Carol J. [11 ]
机构
[1] Univ Pittsburgh, Sch Med, Magee Womens Hosp, Pittsburgh, PA 15260 USA
[2] Univ Minnesota, Sch Med, Dept Lab Med & Pathol & Pediat, Minneapolis, MN 55455 USA
[3] Baylor Coll Med, Dept Pediat, Feigin Ctr, Houston, TX 77030 USA
[4] EMMES Corp, Rockville, MD USA
[5] Med Coll Georgia, Augusta, GA 30912 USA
[6] Planned Parenthood Gulf Coast, Houston, TX USA
[7] Brigham & Womens Hosp, Dept Med, Channing Div Network Med, 75 Francis St, Boston, MA 02115 USA
[8] Harvard Med Sch, Boston, MA 02115 USA
[9] COTA Enterprises, Mclouth, KS USA
[10] Harvard Med Sch, Dept Microbiol & Immunobiol, Div Immunol, Boston, MA 02115 USA
[11] Univ Texas Hlth Sci Ctr Houston, McGovern Med Sch, Dept Pediat, Divs Infect Dis, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
GBS; vaccine; vaginal colonization; rectal colonization; ANTIBODY-RESPONSES; MATERNAL ANTIBODY; DISEASE; IMMUNIZATION; SECRETIONS;
D O I
10.1093/cid/ciy838
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. Group B Streptococcus (GBS) frequently colonizes pregnant women and can cause sepsis and meningitis in young infants. If colonization was prevented through maternal immunization, a reduction in perinatal GBS disease might be possible. A GBS type III capsular polysaccharide (CPS)-tetanus toxoid conjugate (III-TT) vaccine was evaluated for safety and efficacy in preventing acquisition of GBS colonization. Methods. Healthy, nonpregnant women aged 18-40 years and screened to be GBS III vaginal and rectal culture negative were randomized to receive III-TT conjugate or tetanus diphtheria toxoid vaccine in a multicenter, observer-blinded trial. GBS vaginal and rectal cultures and blood were obtained bimonthly over 18 months. Serum concentrations of GBS III CPS-specific antibodies were determined using enzyme-linked immunosorbent assay. Results. Among 1525 women screened, 650 were eligible for the intent-to-treat analysis. For time to first acquisition of vaginal GBS III, vaccine efficacy was 36% (95% confidence interval [CI], 1%-58%; P = .044), and for first rectal acquisition efficacy was 43% (95% CI, 11% to 63%; P = .014). Two months post-immunization, geometric mean concentrations of serum GBS type III CPS-specific immunoglobulin G were 12.6 mu g/mL (95% CI, 9.95 to 15.81) in GBS III-TT recipients, representing a 4-fold increase from baseline in 95% of women, which persisted. Both vaccines were well tolerated. Conclusions. GBS CPS III-TT conjugate vaccine significantly delayed acquisition of vaginal and rectal GBS III colonization. In addition to its use for maternal immunization to passively protect infants with maternally derived antibodies, a multivalent vaccine might also serve to reduce fetal and neonatal exposure to GBS.
引用
收藏
页码:2079 / 2086
页数:8
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