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b型流感嗜血杆菌多糖-破伤风蛋白结合疫苗对既往侵袭性b型流感嗜血杆菌疾病无反应儿童的保护性免疫原性。

Protective immunogenicity of Haemophilus influenzae type b polysaccharide-tetanus protein conjugate vaccine in children who failed to respond to prior invasive H. influenzae type b disease.

作者信息

Berthet F, Prehn A, Suter R, Ethevenaux C, Seger R A

机构信息

Div. Immunology/Haematology, University Children's Hospital Zurich, Switzerland.

出版信息

Pediatr Allergy Immunol. 1998 Aug;9(3):156-60. doi: 10.1111/j.1399-3038.1998.tb00363.x.

Abstract

UNLABELLED

A polyribosylribitol phosphate (polysaccharide)-tetanus protein conjugate vaccine (PRP-T) against Haemophilus influenzae type b (Hib) was evaluated for protective immunogenicity in 25 previously PRP-unimmunized children who had failed to develop protective PRP antibody levels (< 1 microg/ml) after prior invasive Hib disease at median age 10 months. Children under 21 months of age at time of PRP-T immunization received one, two or three doses. Serum was obtained for total PRP antibody, complement mediated bactericidal activity and specific IgG1 and IgG2 PRP antibodies before (n = 25), 1 to 2 months (n = 24) and > 5 months (n = 13) after completed vaccination. One to 2 months after immunization, all but one patient developed > 1 microg/ml of antibody (geometric mean level 50.7 microg/ ml). The non-responder developed protective antibody levels when tested at 6 months after vaccination. Twenty out of 22 sera had detectable complement mediated bactericidal activity (median dilution titer 1:24), 1-2 months after vaccination. Three patients failed to demonstrate PRP antibodies in the IgG1 or IgG2 subclasses, although two of them had protective (> 1 microg/ml) total antibody levels. The second post immunization sera showed persistence of the total PRP antibody levels (geometric mean level 38.2 microg/ml) as well as of the bactericidal activity (median dilution titer 1:32).

CONCLUSION

PRP-T conjugate vaccine is able to elicit a protective immune response in children who have low or unmeasurable PRP antibody levels after a systemic Hib infection.

摘要

未标记

对25名先前未接种多聚核糖基核糖醇磷酸酯(多糖)-破伤风蛋白结合疫苗(PRP-T)的儿童进行了评估,这些儿童在10个月龄时曾患侵袭性b型流感嗜血杆菌(Hib)疾病,且未能产生保护性PRP抗体水平(<1微克/毫升)。在接种PRP-T时年龄小于21个月的儿童接受了1剂、2剂或3剂疫苗。在完成疫苗接种前(n = 25)、接种后1至2个月(n = 24)和>5个月(n = 13)采集血清,检测总PRP抗体、补体介导的杀菌活性以及特异性IgG1和IgG2 PRP抗体。免疫后1至2个月,除1名患者外,所有患者的抗体水平均>1微克/毫升(几何平均水平为50.7微克/毫升)。无反应者在接种疫苗6个月后检测时产生了保护性抗体水平。接种疫苗1至2个月后,22份血清中有20份具有可检测的补体介导杀菌活性(中位稀释效价为1:24)。3名患者在IgG1或IgG2亚类中未检测到PRP抗体,尽管其中2名患者的总抗体水平具有保护性(>1微克/毫升)。第二次免疫后血清显示总PRP抗体水平(几何平均水平为38.2微克/毫升)以及杀菌活性(中位稀释效价为1:32)持续存在。

结论

PRP-T结合疫苗能够在全身性Hib感染后PRP抗体水平低或无法测量的儿童中引发保护性免疫反应。

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