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巴布亚新几内亚高地儿童对多价肺炎球菌疫苗的免疫球蛋白G抗体反应。

Immunoglobulin G antibody responses to polyvalent pneumococcal vaccine in children in the highlands of Papua New Guinea.

作者信息

Pomat W S, Lehmann D, Sanders R C, Lewis D J, Wilson J, Rogers S, Dyke T, Alpers M P

机构信息

Papua New Guinea Institute of Medical Research, Goroka, Eastern Highlands Province.

出版信息

Infect Immun. 1994 May;62(5):1848-53. doi: 10.1128/iai.62.5.1848-1853.1994.

Abstract

The immunoglobulin G (IgG) antibody responses to a pneumococcal polysaccharide vaccine were examined for 480 children aged 3 months to 5 years and living in Tari, Southern Highlands Province, Papua New Guinea. Antipneumococcal IgG to the seven serotypes most frequently causing invasive disease (types 2, 5, 6B, 7F, 14, 19F, and 23F) was measured by an enzyme-linked immunosorbent assay in serum collected before vaccination and 1 and 6 months after vaccination. Prevaccination antibody levels fell rapidly after 3 months of age and remained low throughout the first 2 years of life. One month after vaccination, geometric mean titers of antipneumococcal IgG to serotypes 2, 7F, 23F, and 5 were at least twice those of antibodies in nonvaccinated children of the same age from the ages of 5, 6, 9, and 12 months onwards, respectively; postvaccination antibody responses to serotypes 6B, 14, and 19F rose gradually during the second year of life. Elevated antibody titers to serotypes 2 and 7F were maintained 6 months after vaccination. Thus, young Papua New Guinean children are capable of mounting a good immune response to some pneumococcal capsular polysaccharides from a young age, and the antibody responses to capsular polysaccharides are consistent with studies in developed countries. However, in Papua New Guinea, the serogroup distribution of invasive disease matches the immunogenic components of the pneumococcal polysaccharide vaccine more closely than in developed countries, a fact which helps to explain the results of controlled trials in Papua New Guinea, in which this vaccine prevented death and severe morbidity from pneumonia in young children.

摘要

对生活在巴布亚新几内亚南部高地省塔里的480名3个月至5岁儿童,检测了其对肺炎球菌多糖疫苗的免疫球蛋白G(IgG)抗体反应。通过酶联免疫吸附测定法,在接种疫苗前以及接种后1个月和6个月采集的血清中,检测了针对7种最常引起侵袭性疾病的血清型(2、5、6B、7F、14、19F和23F)的抗肺炎球菌IgG。接种疫苗前的抗体水平在3个月龄后迅速下降,并在生命的头两年一直保持在低水平。接种疫苗1个月后,针对血清型2、7F、23F和5的抗肺炎球菌IgG几何平均滴度,分别从5、6、9和12个月龄起,至少是同年龄未接种疫苗儿童抗体滴度的两倍;接种疫苗后对血清型6B、14和19F的抗体反应在生命的第二年逐渐上升。接种疫苗6个月后,针对血清型2和7F的抗体滴度仍维持在较高水平。因此,巴布亚新几内亚幼儿能够从幼年起就对某些肺炎球菌荚膜多糖产生良好的免疫反应,并且对荚膜多糖的抗体反应与发达国家的研究结果一致。然而,在巴布亚新几内亚,侵袭性疾病的血清群分布比在发达国家更紧密地匹配肺炎球菌多糖疫苗的免疫原性成分,这一事实有助于解释在巴布亚新几内亚进行的对照试验结果,即这种疫苗预防了幼儿因肺炎导致的死亡和严重发病。

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