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低剂量BioHepB免疫儿童后对前S成分的抗体反应。

Antibody responses to preS components after immunization of children with low doses of BioHepB.

作者信息

Madalinski K, Sylvan S P, Hellström U, Mikolajewicz J, Zembrzuska-Sadkowska E, Piontek E

机构信息

Department of Immunology, Child Health Memorial Institute, Al. Dzieci Polskich 20, 04-736, Warsaw, Poland.

出版信息

Vaccine. 2001 Oct 12;20(1-2):92-7. doi: 10.1016/s0264-410x(01)00312-7.

Abstract

BioHepB is a recombinant, hepatitis B vaccine derived from a mammalian cell line and containing HBs as well as preS1 and preS2 antigens, in their glycosylated and non-glycosylated forms. The vaccine was administered intramuscularly to 18 children aged 5 months to 11 years at 0, 1 and 6 months. One hundred percent seroconversion and seroprotection rates were achieved after primary and secondary immunization with the 2.5 microg doses of BioHepB. Ten out of the 18 children (56%) responded with the appearance of anti-preS1 and/or anti-preS2 antibodies in circulation, when analyzed 1, 2, 6, 7 and 12 months after the initiation of vaccination. In comparison with the emergence of the anti-HBs response, early (month 2, after two injections) or late (month 7, after three injections) peak responses were noted for the kinetics of anti-preS1 and anti-preS2 production during the course of immunization, demonstrating that the anti-preS1 and anti-preS2 responses are differently regulated, compared with the anti-HBs response. At month 6, just prior to the final injection, BioHepB caused significantly higher anti-HBs responses (GMT) in preS1-reactive children than in children without preS1 antibodies (P<0.005). Moreover, a significantly higher, anti-HBs response in GMT was also noted for anti-preS2-reactive children compared with anti-preS2-negative children (P<0.05). These findings demonstrated that recognition of the preS epitopes contained in the experimental preS1/preS2/S vaccine is accompanied by a more rapid onset and pronounced antibody response to the S-gene-derived protein in healthy children.

摘要

BioHepB是一种重组乙肝疫苗,源自哺乳动物细胞系,含有糖基化和非糖基化形式的乙肝表面抗原(HBs)以及前S1和前S2抗原。该疫苗于0、1和6个月时对18名年龄在5个月至11岁的儿童进行肌肉注射。使用2.5微克剂量的BioHepB进行初次和二次免疫后,血清转化率和血清保护率均达到100%。在接种疫苗后1、2、6、7和12个月进行分析时,18名儿童中有10名(56%)循环中出现了抗前S1和/或抗前S2抗体。与抗HBs反应的出现相比,在免疫过程中,抗前S1和抗前S2产生的动力学呈现出早期(第2个月,两次注射后)或晚期(第7个月,三次注射后)的峰值反应,表明与抗HBs反应相比,抗前S1和抗前S2反应受到不同的调节。在第6个月,即在最后一次注射前,BioHepB在有前S1反应性的儿童中引起的抗HBs反应(几何平均滴度)显著高于无前S1抗体的儿童(P<0.005)。此外,与抗前S2阴性儿童相比,抗前S2反应性儿童的抗HBs反应在几何平均滴度上也显著更高(P<0.05)。这些发现表明,在健康儿童中,识别实验性前S1/前S2/S疫苗中包含的前S表位伴随着对S基因衍生蛋白更快的抗体反应起始和更明显的抗体反应。

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