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两种b型流感嗜血杆菌结合疫苗加强剂量的研究,包括它们的互换性。

Study of booster doses of two Haemophilus influenzae type b conjugate vaccines including their interchangeability.

作者信息

Scheifele D, Law B, Mitchell L, Ochnio J

机构信息

Vaccine Evaluation Center, BC's Children's Hospital, Vancouver, Canada.

出版信息

Vaccine. 1996 Oct;14(15):1399-406. doi: 10.1016/s0264-410x(96)00086-2.

Abstract

A prospective, two center study of 319 children was undertaken to assess responses to booster immunization in healthy 18-month-olds who completed primary immunization 12 months earlier with Haemophilus influenzae type b (Hib) conjugate vaccine (either HbOC or PRP-T). Interchangeability of these products as boosters was also assessed, using combination products containing diphtheria, pertussis and tetanus components. The study was randomized and evaluator blinded. Sera obtained prior to booster vaccination and 4 weeks later were tested for anti-PRP using an IgG-specific enzyme immunoassay. Pre-immunization anti-PRP levels were low: unmeasurable levels (< 0.06 microgram ml-1) were present in 47% of those primed with HbOC and 35% of those primed with PRP-T (P < 0.05). Most children responded strongly to booster vaccination. Interchanging the products had no detrimental effect. Children who lacked measurable antibody prior to re-vaccination had significantly weaker responses 4 weeks afterward. Earlier Hib booster vaccination should be considered in Canada to avoid low anti-PRP trough levels. Extended follow-up of antibody levels and vaccine protective efficacy is also advisable given the observed heterogeneity of responses to booster vaccination.

摘要

开展了一项前瞻性、双中心研究,纳入319名儿童,以评估健康的18个月大儿童对加强免疫的反应。这些儿童在12个月前已完成b型流感嗜血杆菌(Hib)结合疫苗(HbOC或PRP-T)的基础免疫。还使用含有白喉、百日咳和破伤风成分的联合产品评估了这些产品作为加强剂的互换性。该研究采用随机分组且评估者设盲。在加强疫苗接种前及4周后采集血清,使用IgG特异性酶免疫测定法检测抗PRP水平。基础免疫前抗PRP水平较低:用HbOC进行基础免疫的儿童中47%抗PRP水平不可测(<0.06微克/毫升),用PRP-T进行基础免疫的儿童中35%抗PRP水平不可测(P<0.05)。大多数儿童对加强疫苗接种反应强烈。互换产品没有不良影响。再次接种前缺乏可测抗体的儿童在4周后的反应明显较弱。在加拿大应考虑更早进行Hib加强疫苗接种,以避免抗PRP谷值水平过低。鉴于观察到加强疫苗接种反应存在异质性,对抗体水平和疫苗保护效力进行延长随访也是可取的。

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