流感嗜血杆菌b型结合疫苗(磷酸多核糖苷糖醇-破伤风类毒素结合物)诱导的功能性抗体活性

S. Romero-Steiner, Josefina Fernández, Christel Biltoft, Melissa E. Wohl, Jacqueline Sánchez, J. Feris, S. Balter, O. Levine, G. Carlone
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引用次数: 48

摘要

摘要:本研究采用硫氰酸钠(NaSCN)洗涤法,对接种流感嗜血杆菌b型偶联疫苗(聚核糖苷糖醇磷酸[PRP]与破伤风类毒素[PRP- t]结合)后产生的抗体功能活性、血清杀菌活性(SBA)和免疫球蛋白G (IgG)抗体亲和度指标进行了评价。来自多米尼加共和国的600名婴儿在2、4和6个月时随机接受三种PRP- t疫苗方案中的一种:全剂量(PRP抗原10 μg)、半剂量(5.0 μg)和三分之一剂量(3.3 μg) (J. Fernandez等人,Am. Fernandez等人)。j .太多。医学卫生62:485-490,2000)。随机选取年龄为7月龄,血清中抗prp IgG含量≥2.0 μg / ml的60份血清进行抗体测定。接受全剂量(n = 19)、半剂量(n = 19)和三分之一剂量(n = 22)治疗的婴儿的几何平均IgG浓度分别为13、14和17 μg/ml。在接受全剂量、半剂量和三分之一剂量方案的婴儿血清中,SBA几何平均滴度(1/稀释)分别为85.0、82.0和76.1。全剂量、半剂量和三剂量方案的贪婪指数(平均±标准误差加权平均值NaSCN摩尔浓度×血清稀释因子)分别为71.9±9.4、123.6±26.8和150.9±24.9。经过比较,发现唯一显著差异(P = 0.024)是接受三次剂量方案的婴儿血清的贪婪指数高于接受全剂量方案的婴儿血清。我们得出的结论是,在每毫升抗prp IgG≥2 μg的婴儿中,小剂量可引起类似的功能抗体活性,分别对应于89%,90%和97%的婴儿接受三次剂量的全浓度或标记浓度的一半或三分之一。这种方法为资源有限的国家预防b型流感嗜血杆菌疾病提供了另一种战略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functional Antibody Activity Elicited by Fractional Doses ofHaemophilus influenzae Type b Conjugate Vaccine (Polyribosylribitol Phosphate–Tetanus Toxoid Conjugate)
ABSTRACT We evaluated the functional activities of antibodies, serum bactericidal activity (SBA), and immunoglobulin G (IgG) antibody avidity indices, using sodium thiocyanate (NaSCN) elution, elicited after vaccination with fractional doses of the Haemophilus influenzae type b conjugate (polyribosylribitol phosphate [PRP] conjugated to tetanus toxoid [PRP-T]) vaccine. A cohort of 600 infants from the Dominican Republic were randomized to receive one of three regimens of the PRP-T vaccine at ages 2, 4, and 6 months: full doses (10 μg of PRP antigen), one-half doses (5.0 μg), and one-third doses (3.3 μg) (J. Fernandez et al., Am. J. Trop. Med. Hyg. 62:485–490, 2000). Sixty serum samples, collected at age 7 months, with ≥2.0 μg of anti-PRP IgG per ml were randomly selected for avidity determinations. Geometric mean IgG concentrations were 13, 14, and 17 μg/ml for infants who received the full-dose (n = 19), one-half-dose (n = 19), and one-third-dose (n = 22) regimens, respectively. SBA geometric mean titers (1/dilution) were 85.0, 82.0, and 76.1 in sera from infants receiving the full-, one-half-, and one-third-dose regimens, respectively. Avidity indices (mean ± standard error weighted average of NaSCN molar concentration × serum dilution factor) were 71.9 ± 9.4, 123.6 ± 26.8, and 150.9 ± 24.9 for the full-, one-half-, and one-third-dose regimens, respectively. Upon comparison, the only significant difference (P = 0.024) found was a greater avidity index for sera from infants receiving the one-third-dose regimen than for sera from infants receiving the the full-dose regimen. We conclude that fractional doses elicit similar functional antibody activities in infants with ≥2 μg of anti-PRP IgG per ml, corresponding to 89, 90, and 97% of infants receiving three doses of either the full concentration or one-half or one-third of the labeled concentration, respectively. This approach offers an alternative strategy for the prevention of H. influenzae type b disease in countries with limited resources.
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