Romero-Steiner S, Fernandez J, Biltoft C, Wohl M E, Sanchez J, Feris J, Balter S, Levine O S, Carlone G M
Immunology Section, Respiratory Diseases Branch, Division of Bacterial and Mycotic Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA.
Clin Diagn Lab Immunol. 2001 Nov;8(6):1115-9. doi: 10.1128/CDLI.8.6.1115-1119.2001.
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 microg of PRP antigen), one-half doses (5.0 microg), and one-third doses (3.3 microg) (J. Fernandez et al., Am. J. Trop. Med. Hyg. 62:485-490, 2000). Sixty serum samples, collected at age 7 months, with > or =2.0 microg of anti-PRP IgG per ml were randomly selected for avidity determinations. Geometric mean IgG concentrations were 13, 14, and 17 microg/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 x 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 > or = 2 microg 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.
我们使用硫氰酸钠(NaSCN)洗脱法,评估了用b型流感嗜血杆菌结合疫苗(多聚核糖磷酸[PRP]与破伤风类毒素[PRP-T]结合)小剂量接种后诱导产生的抗体功能活性、血清杀菌活性(SBA)以及免疫球蛋白G(IgG)抗体亲和力指数。来自多米尼加共和国的600名婴儿队列被随机分为三组,在2、4和6月龄时分别接受三种PRP-T疫苗接种方案之一:全剂量(10μg PRP抗原)、半剂量(5.0μg)和三分之一剂量(3.3μg)(J. Fernandez等人,《美国热带医学与卫生杂志》62:485 - 490,2000年)。在7月龄时收集了60份血清样本,随机选取每毫升抗PRP IgG≥2.0μg的样本进行亲和力测定。接受全剂量方案(n = 19)、半剂量方案(n = 19)和三分之一剂量方案(n = 22)的婴儿,其几何平均IgG浓度分别为13、14和17μg/ml。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/稀释倍数)分别为85.0、82.0和76.1。全剂量、半剂量和三分之一剂量方案的亲和力指数(NaSCN摩尔浓度×血清稀释因子的平均±标准误加权平均值)分别为71.9±9.4、123.6±26.8和150.9±24.9。经比较,发现的唯一显著差异(P = 0.024)是接受三分之一剂量方案的婴儿血清的亲和力指数高于接受全剂量方案的婴儿血清。我们得出结论,对于每毫升抗PRP IgG≥2μg的婴儿,小剂量接种诱导产生的功能性抗体活性相似,这分别对应于接受全浓度三剂、半浓度三剂或三分之一标记浓度三剂的婴儿中的89%、90%和97%。这种方法为资源有限国家预防b型流感嗜血杆菌疾病提供了一种替代策略。