Maternal Immunization Earlier in Pregnancy Maximizes Antibody Transfer and Expected Infant Seropositivity Against Pertussis

被引:181
作者
Eberhardt, Christiane S. [1 ,2 ]
Blanchard-Rohner, Geraldine [3 ]
Lemaitre, Barbara [1 ]
Boukrid, Meriem [4 ]
Combescure, Christophe [5 ,6 ]
Othenin-Girard, Veronique [4 ]
Chilin, Antonina [4 ]
Petre, Jean [7 ]
de Tejada, Begona Martinez [4 ]
Siegrist, Claire-Anne [1 ,3 ]
机构
[1] Univ Hosp Geneva, Dept Pediat & Pathol Immunol, Ctr Vaccinol & Neonatal Immunol, CH-1211 Geneva 4, Switzerland
[2] Univ Hosp Geneva, Dept Neonatol & Pediat Intens Care, CH-1211 Geneva 4, Switzerland
[3] Univ Hosp Geneva, Dept Pediat, Childrens Hosp Geneva, CH-1211 Geneva 4, Switzerland
[4] Univ Hosp Geneva, Dept Gynecol & Obstet, CH-1211 Geneva 4, Switzerland
[5] Univ Hosp Geneva, Clin Res Ctr, CH-1211 Geneva 4, Switzerland
[6] Univ Geneva, Fac Med, CH-1211 Geneva 4, Switzerland
[7] BioNet Asia Co Ltd, Bangkok, Thailand
关键词
pertussis; maternal immunization; maternal antibodies; pregnancy; neonates; BORDETELLA-PERTUSSIS; TDAP IMMUNIZATION; NEONATAL VACCINATION; IMMUNE-RESPONSES; DIPHTHERIA; TETANUS; PRETERM; TOXIN; IMMUNOGENICITY; MOTHERS;
D O I
10.1093/cid/ciw027
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Background. Maternal immunization against pertussis is currently recommended after the 26th gestational week (GW). Data on the optimal timing of maternal immunization are inconsistent. Methods. We conducted a prospective observational noninferiority study comparing the influence of second-trimester (GW 13-25) vs third-trimester (>= GW 26) tetanus-diphtheria-acellular pertussis (Tdap) immunization in pregnant women who delivered at term. Geometric mean concentrations (GMCs) of cord blood antibodies to recombinant pertussis toxin (PT) and filamentous hemagglutinin (FHA) were assessed by enzyme-linked immunosorbent assay. The primary endpoint were GMCs and expected infant seropositivity rates, defined by birth anti-PT > 30 enzyme-linked immunosorbent assay units (EU)/mL to confer seropositivity until 3 months of age. Results. We included 335 women (mean age, 31.0 +/- 5.1 years; mean gestational age, 39.3 +/- 1.3 GW) previously immunized with Tdap in the second (n = 122) or third (n = 213) trimester. Anti-PT and anti-FHA GMCs were higher following second-vs third-trimester immunization (PT: 57.1 EU/mL [95% confidence interval {CI}, 47.8-68.2] vs 31.1 EU/mL [95% CI, 25.7-37.7], P <.001; FHA: 284.4 EU/mL [95% CI, 241.3-335.2] vs 140.2 EU/mL [95% CI, 115.3-170.3], P <.001). The adjusted GMC ratios after second-vs third-trimester immunization differed significantly (PT: 1.9 [95% CI, 1.4-2.5]; FHA: 2.2 [95% CI, 1.7-3.0], P <.001). Expected infant seropositivity rates reached 80% vs 55% following second-vs third-trimester immunization (adjusted odds ratio, 3.7 [95% CI, 2.1-6.5], P <.001). Conclusions. Early second-trimester maternal Tdap immunization significantly increased neonatal antibodies. Recommending immunization from the second trimester onward would widen the immunization opportunity window and could improve seroprotection.
引用
收藏
页码:829 / 836
页数:8
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