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b型流感嗜血杆菌疫苗在基础免疫程序中的可互换性:两剂混合免疫方案的评估

Interchangeability of Haemophilus influenzae type b vaccines in the primary series: evaluation of a two-dose mixed regimen.

作者信息

Bewley K M, Schwab J G, Ballanco G A, Daum R S

机构信息

Department of Pediatrics, University of Chicago, IL, USA.

出版信息

Pediatrics. 1996 Nov;98(5):898-904.

PMID:8909483
Abstract

OBJECTIVE

To evaluate two- or three-dose "mixed" regimens of Haemophilus influenzae type b conjugate vaccines in the priming series.

DESIGN

Two randomized clinical trials with 140 and 181 infants, respectively.

SETTING

Private practices in New Orleans and Chicago.

METHODS

In trial I, infants received one of four regimens. Two were recommended regimens for polyribosylribitol phosphate (PRP)-meningococcal protein conjugate (M) and PRP-tetanus toxoid conjugate (T). Two mixed regimens consisted of M at 2 months followed by two doses of T or PRP-diphtheria toxoid conjugate (D) at 4 and 6 months. Trial II consisted of three groups. Two were recommended regimens for M and T. The third was a two-dose mixed regimen consisting of M at 2 months and T at 4 months. Parents were interviewed and instructed to record side effects after each vaccination. Serum was assayed for H influenzae type b anticapsular antibody (anti-PRP).

RESULTS

Minor differences in safety profiles likely reflected alpha error. In trial I, M (lot 0884T, one of several known to have had decreased immunogenicity), probably primed for substantial increase in serum antibody when D or T was given at 4 and 6 months. In trial II, infants who received the two-dose mixed regimen (M from immunogenic lot 0116W at 2 months and T at 4 months) had a significantly higher mean area under the curve than recipients of the three-dose TTT regimen when antibody concentration was plotted against age, although the geometric mean anti-PRP antibody concentration for the MT-recipients was significantly lower at 7 months.

CONCLUSIONS

M used in trial I may have primed infants despite poor immunogenicity. The two-dose mixed regimen (MT-) in trial II produced a mean anti-PRP antibody concentration with higher sustained anti-PRP concentrations from 2 to 7 months, as judged by the area under the curve, but a lower mean anti-PRP antibody concentration at 7 months.

摘要

目的

评估b型流感嗜血杆菌结合疫苗在初始免疫程序中的两剂或三剂“混合”方案。

设计

两项分别纳入140名和181名婴儿的随机临床试验。

地点

新奥尔良和芝加哥的私人诊所。

方法

在试验I中,婴儿接受四种方案之一。两种是多聚核糖磷酸(PRP)-脑膜炎球菌蛋白结合物(M)和PRP-破伤风类毒素结合物(T)的推荐方案。两种混合方案包括2月龄时接种M,随后在4月龄和6月龄接种两剂T或PRP-白喉类毒素结合物(D)。试验II包括三组。两组是M和T的推荐方案。第三组是两剂混合方案,包括2月龄时接种M,4月龄时接种T。对家长进行访谈,并指导他们记录每次接种后的副作用。检测血清中的b型流感嗜血杆菌抗荚膜抗体(抗PRP)。

结果

安全性方面的微小差异可能反映了第一类错误。在试验I中,M(批次0884T,已知免疫原性降低的几个批次之一),当在4月龄和6月龄接种D或T时,可能引发血清抗体大幅增加。在试验II中,当将抗体浓度与年龄作图时,接受两剂混合方案(2月龄时接种来自免疫原性批次0116W的M,4月龄时接种T)的婴儿的曲线下平均面积显著高于接受三剂TTT方案的婴儿,尽管MT组婴儿在7月龄时的几何平均抗PRP抗体浓度显著较低。

结论

试验I中使用的M尽管免疫原性较差,但可能已使婴儿产生了免疫启动。试验II中的两剂混合方案(MT-)产生的平均抗PRP抗体浓度,根据曲线下面积判断,在2至7个月期间具有更高的持续抗PRP浓度,但在7月龄时平均抗PRP抗体浓度较低。

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