Omeñaca Felix, Garcia-Sicilia José, García-Corbeira Pilar, Boceta Reyes, Torres Victorio
Department of Neonatology, La Paz Hospital, Madrid, Spain.
Pediatrics. 2007 Jan;119(1):e179-85. doi: 10.1542/peds.2005-2907. Epub 2006 Dec 4.
Prematurity may be a risk factor for Haemophilus influenzae type b vaccine failure. This article evaluates the Haemophilus influenzae type b immunogenicity of a hexavalent diphtheria-tetanus-acellular pertussis-hepatitis B-inactivated poliovirus/Haemophilus influenzae type b vaccine in preterm infants (< 37 weeks' gestation).
This was an open-label, parallel group study. Preterm (N = 94) and term infants (N = 92) received 3 doses of a diphtheria-tetanus-acellular pertussis-hepatitis B-inactivated poliovirus/Haemophilus influenzae type b vaccine at 2, 4, and 6 months with a booster dose at 18 to 20 months. Antipolyribosyl ribitol phosphate antibody concentrations were determined in serum samples taken before and 1 month after primary and booster vaccination.
Postprimary seroprotection rates (antipolyribosyl ribitol phosphate > or = 0.15 microg/mL) were lower in preterm than in term infants (92.5% vs 97.8%), with antipolyribosyl ribitol phosphate geometric mean concentrations of 2.241 vs 4.247 microg/mL. A progressive reduction in immune response to the Haemophilus influenzae type b antigen was observed with decreasing length of gestation and decreasing birth weight when cutoff > or = 1 microg/mL was considered. Prebooster seroprotection rates and antipolyribosyl ribitol phosphate geometric mean concentrations were low in both groups (antipolyribosyl ribitol phosphate > or = 1.0 microg/mL in 10.7% of preterm and 28.4% of term infants). A vigorous response to booster vaccination was seen in both groups, with no differences in postbooster seroprotection rates or antipolyribosyl ribitol phosphate geometric mean concentrations between the 2 groups (antipolyribosyl ribitol phosphate > or = 1.0 microg/mL in 100% of preterm and 98.5% of term infants).
Primary vaccination with a hexavalent diphtheria-tetanus-acellular pertussis-hepatitis B-inactivated poliovirus/Haemophilus influenzae type b vaccine at 2, 4, and 6 months with a booster dose at 18 to 20 months elicits a satisfactory antipolyribosyl ribitol phosphate response in preterm infants compared with term controls. Immunologic response decreased with decreased gestational age and birth weight.
早产可能是b型流感嗜血杆菌疫苗接种失败的一个风险因素。本文评估了一种六价白喉-破伤风-无细胞百日咳-乙型肝炎-灭活脊髓灰质炎病毒/b型流感嗜血杆菌疫苗在早产儿(妊娠<37周)中的b型流感嗜血杆菌免疫原性。
这是一项开放标签的平行组研究。早产儿(N = 94)和足月儿(N = 92)在2、4和6个月时接种3剂白喉-破伤风-无细胞百日咳-乙型肝炎-灭活脊髓灰质炎病毒/b型流感嗜血杆菌疫苗,并在18至20个月时接种加强剂。在初次和加强疫苗接种前及接种后1个月采集的血清样本中测定抗聚核糖核糖醇磷酸抗体浓度。
早产儿初次接种后的血清保护率(抗聚核糖核糖醇磷酸≥0.15μg/mL)低于足月儿(92.5%对97.8%),抗聚核糖核糖醇磷酸几何平均浓度分别为2.241μg/mL和4.247μg/mL。当临界值≥1μg/mL时,观察到随着胎龄和出生体重的降低,对b型流感嗜血杆菌抗原的免疫反应逐渐降低。两组在加强疫苗接种前的血清保护率和抗聚核糖核糖醇磷酸几何平均浓度均较低(10.7%的早产儿和28.4%的足月儿抗聚核糖核糖醇磷酸≥1.0μg/mL)。两组对加强疫苗接种均有强烈反应,两组在加强疫苗接种后的血清保护率或抗聚核糖核糖醇磷酸几何平均浓度无差异(100%的早产儿和98.5%的足月儿抗聚核糖核糖醇磷酸≥1.0μg/mL)。
与足月儿对照相比,在2、4和6个月时接种六价白喉-破伤风-无细胞百日咳-乙型肝炎-灭活脊髓灰质炎病毒/b型流感嗜血杆菌疫苗并在18至20个月时接种加强剂,在早产儿中引发了令人满意的抗聚核糖核糖醇磷酸反应。免疫反应随着胎龄和出生体重的降低而降低。