[b-破伤风嗜血杆菌蛋白偶联物(PRP-T)在儿童镰状细胞性贫血中的免疫原性和耐受性]。

Archives francaises de pediatrie Pub Date : 1993-12-01
M de Montalembert, P Bégué, B Fritzell, P Houmeau
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引用次数: 0

摘要

背景:患有镰状细胞性贫血的婴幼儿感染b型流感嗜血杆菌的风险增加。本报告描述了b型流感嗜血杆菌结合疫苗在这类儿童中的免疫原性和安全性。人群与方法:研究了111名6个月~ 11岁的儿童(平均3.7岁)。他们属于巴黎地区600多名患有镰状细胞性贫血的儿童。经父母同意后,他们被注射一次(肌肉注射或皮下注射)b型流感嗜血杆菌破伤风类毒素结合疫苗(0.5 ml)。记录3天内的不良反应。在注射前、一个月和一年后分别测定特异性抗体的滴度。结果:疫苗耐受性良好,仅局部反应:5例患儿出现红斑反应,30例患儿出现疼痛。在6个月至3岁的儿童中,接种后1个月,平均抗体滴度从0.09微克/毫升增加到20.6微克/毫升;3 ~ 11岁儿童的平均滴度由0.44微克/毫升上升至56.86微克/毫升。接种疫苗一年后,61名儿童中检测到的滴度在92%的6个月至3岁儿童中超过1微克/毫升,在100%的年龄较大的儿童中超过1微克/毫升。结论:该疫苗具有免疫原性和良好的耐受性。因此,建议6个月以上镰状细胞性贫血儿童的疫苗接种时间表与正常儿童相同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Immunogenicity and tolerability of Haemophilus b-tetanus protein conjugate (PRP-T) in children with sickle cell anemia].

Background: Infants and young children with sickle cell anemia are at increased risk of infection with Haemophilus influenzae type b. This report describes the immunogenicity and safety of Haemophilus b conjugate vaccine in such children.

Population and methods: One hundred and eleven children aged 6 months-11 years (mean: 3.7 years) were studied. They belonged to a cohort of over 600 children in the Paris area that have sickle cell anemia. After parental consent, they were given one injection (intramuscularly or subcutaneously) of Haemophilus influenzae type b-tetanus toxoid conjugate vaccine (0.5 ml). Any adverse reactions during the following 3 days were noted. Titers of specific antibodies were measured just before injection, one month, and one year later.

Results: The vaccine was well tolerated, with only local reactions: erythematous reactions in 5 children and pain in 30. In the children aged 6 months-3 years, the mean antibody titers increased from 0.09 to 20.6 micrograms/ml, 1 month after the vaccination; in those aged 3-11 years, the mean titer increased from 0.44 to 56.86 micrograms/ml. One year after vaccination, the titers measured in 61 children were over 1 microgram/ml in 92% of children aged 6 months-3 years and in 100% of the older children.

Conclusion: This type of vaccine is immunogenic and well tolerated. Thus the vaccination schedule recommended for children with sickle cell anemia aged over 6 months is the same as that for normal children.

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