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首页> 外文期刊>Clinical infectious diseases >Importance of timing of maternal combined tetanus, diphtheria, and acellular pertussis (Tdap) immunization and protection of young infants
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Importance of timing of maternal combined tetanus, diphtheria, and acellular pertussis (Tdap) immunization and protection of young infants

机译:产妇破伤风,白喉和脱细胞百日咳(Tdap)联合免疫及保护婴儿时机的重要性

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Background. Pertussis booster vaccine (Tdap) recommendations assume that pertussis-specific antibodies in women immunized preconception, during, or after previous pregnancies persist at sufficient levels to protect newborn infants.Methods. Pertussis-specific immunoglobulin G (IgG) was measured by IgG-specific enzyme-linked immunosorbent assay (ELISA) in maternal-umbilical cord serum pairs where mothers received Tdap during the prior 2 years. Geometric mean concentrations (GMCs) of pertussis antibodies and cord-maternal GMC ratios were calculated.Results. One hundred five mothers (mean age, 25.3 years [range, 15.3-38.4 years]; mean gestation, 39 weeks [range, 37-43 weeks]) immunized with Tdap vaccine a mean of 13.7 months (range, 2.3-23.9 months) previously were included; 72 (69%) had received Tdap postpartum, 31 at a routine healthcare visit and 2 as contacts of another newborn. There was no difference in GMCs for pertussis-specific IgG in maternal delivery or infant cord sera for women immunized before (n = 86) or during (n = 19) early pregnancy. Placental transport of antibodies was 121%-186% from mothers immunized before and during pregnancy, respectively. Estimated GMC of IgG to pertussis toxin was <5 ELISA units (EU)/mL at infant age 2 months (start of infant immunization series). More infants of mothers immunized during pregnancy had pertussis toxin levels estimated to be higher than the lower limit of quantitation of the assay (4 EU/mL) through age 2 months (52% vs 38%; P =. 34). Conclusions. Infants of mothers immunized preconception or in early pregnancy have insufficient pertussis-specific antibodies to protect against infection. Maternal immunization during the third trimester, immunization of other infant contacts, and reimmunization during subsequent pregnancies may be necessary. ? 2012 The Author 2012. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.
机译:背景。百日咳加强疫苗(Tdap)的建议是假设在怀孕前,怀孕期间或之后免疫的妇女中,百日咳特异性抗体的存在水平足以保护新生儿。百日咳特异性免疫球蛋白G(IgG)是通过IgG特异性酶联免疫吸附测定(ELISA)在母体-脐带血清对中测量的,母亲在前2年中接受了Tdap。计算百日咳抗体的几何平均浓度(GMCs)和脐带母体GMC的比率。接受Tdap疫苗免疫的155名母亲(平均年龄25.3岁[范围:15.3-38.4岁];平均妊娠39周[范围37-43周])平均接种了13.7个月(2.3-23.9个月)以前包括在内; 72名(69%)产后接受了Tdap的治疗,例行常规医疗访问中接受了31次,另外2名新生儿进行了接触。早产前(n = 86)或怀孕期间(n = 19)进行免疫接种的妇女,百日咳特异性IgG的GMC在产妇分娩或婴儿脐带血清中无差异。妊娠前和妊娠期间免疫的母亲的胎盘抗体转运率分别为121%-186%。在婴儿2个月大时(婴儿免疫系列开始),IgG对百日咳毒素的GMC估计值<5 ELISA单位(EU)/ mL。到2个月大时,更多在怀孕期间接受免疫接种的母亲的百日咳毒素水平高于该分析的定量下限(4 EU / mL)(52%vs 38%; P =。34)。结论怀孕前或怀孕初期进行免疫接种的母亲的婴儿,百日咳特异性抗体不足以预防感染。可能需要在孕晚期进行母体免疫,对其他婴儿接触者进行免疫,并在随后的怀孕期间进行再次免疫。 ? 2012作者2012。由牛津大学出版社代表美国传染病学会出版。版权所有。有关许可,请发送电子邮件至:journals.permissions@oup.com。

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