Zepp F, Schmitt H J, Kaufhold A, Schuind A, Knuf M, Habermehl P, Meyer C, Bogaerts H, Slaoui M, Clemens R
Children's Hospital, Johannes Gutenberg University, Mainz, Germany.
Eur J Pediatr. 1997 Jan;156(1):18-24. doi: 10.1007/s004310050544.
The lack of an adequate immune response to the major polysaccharide of the Haemophilus influenzae type b (Hib) capsule (polyribosyl ribitol phosphate) (PRP) in very young infants (< 18 months) can be overcome by conjugating PRP to a T-cell dependent carrier protein. We studied whether administration of a tetanus-PRP conjugate vaccine reconstituted with a diphtheria-tetanus-acellular pertussis-hepatitis B (DTPa-HBV) vaccine as a three dose primary course at 3, 4 and 5 months of age induced PRP-specific immunological memory, by examining the anti-PRP response to a dose of unconjugated PRP given with the DTPa-HBV booster approximately 1 year later. The unconjugated PRP elicited protective anti-PRP antibody levels (> or = 0.15 microgram/ml) in all but 3 of the 369 vaccinees, including 13 infants who failed to demonstrate a measurable immune response after the primary course. In a sub-cohort of 54 subjects all had anti-PRP levels > or = 0.5 microgram/ml within 7-14 days of the booster showing a rapid anamnestic type response. Both primary and booster responses were predominantly IgGl indicating a T-cell dependent response. The DTPa-HBV components elicited protective anti-diphtheria, anti-tetanus and anti-HBs antibody levels in > or = 98.5% of vaccinees, and immune responses to each of the acellular pertussis vaccine components in 92.3%-97.3% of subjects.
The tetanus-PRP conjugate vaccine not only elicited a good primary humoral response, but also induced immunological memory so that the infants were able to mount a large and rapid immune response to subsequent exposure to plain PRP, indicating that protection against circulating wild-type Hib had been generated. Successful induction of immunological memory occurred even when there was no measurable humoral anti-PRP response to the primary course. Tetanus-PRP conjugate vaccine can be used in combination with DTPa-HBV vaccine, when administered separately or as a single injection in the same syringe, in primary immunisation schedules at 3, 4 and 5 months of age.
在非常年幼的婴儿(<18个月)中,对b型流感嗜血杆菌(Hib)荚膜的主要多糖(多聚核糖基核糖醇磷酸酯)(PRP)缺乏足够的免疫反应,可通过将PRP与T细胞依赖性载体蛋白偶联来克服。我们研究了在3、4和5月龄时作为三剂基础免疫程序给予用白喉-破伤风-无细胞百日咳-乙型肝炎(DTPa-HBV)疫苗复溶的破伤风-PRP结合疫苗,是否能诱导PRP特异性免疫记忆,方法是在大约1年后与DTPa-HBV加强疫苗一起给予一剂未结合的PRP时检测抗PRP反应。在369名接种疫苗者中,除3人外,所有未结合的PRP均引发了保护性抗PRP抗体水平(≥0.15微克/毫升),其中包括13名在基础免疫程序后未能显示出可测量免疫反应的婴儿。在一个54名受试者的亚组中,所有人在加强疫苗接种后7-14天内抗PRP水平≥0.5微克/毫升,显示出快速的回忆型反应。基础免疫和加强免疫反应主要都是IgG1,表明是T细胞依赖性反应。DTPa-HBV成分在≥98.5%的接种疫苗者中引发了保护性抗白喉、抗破伤风和抗-HBs抗体水平,并且在92.3%-97.3%的受试者中引发了对每种无细胞百日咳疫苗成分的免疫反应。
破伤风-PRP结合疫苗不仅引发了良好的基础体液反应,还诱导了免疫记忆,使婴儿能够对随后接触未结合的PRP产生强烈而快速的免疫反应,表明已产生针对循环野生型Hib的保护作用。即使基础免疫程序没有可测量的体液抗PRP反应,也成功诱导了免疫记忆。破伤风-PRP结合疫苗可与DTPa-HBV疫苗联合使用,分别给药或在同一注射器中单次注射,用于3、4和5月龄的基础免疫程序。