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巴西儿童对B群脑膜炎奈瑟菌外膜蛋白疫苗的免疫反应:与疗效比较。

Immune response of Brazilian children to a Neisseria meningitidis serogroup B outer membrane protein vaccine: comparison with efficacy.

作者信息

Milagres L G, Ramos S R, Sacchi C T, Melles C E, Vieira V S, Sato H, Brito G S, Moraes J C, Frasch C E

机构信息

Bacteriology Division, Adolfo Lutz Institute, São Paulo, Brazil.

出版信息

Infect Immun. 1994 Oct;62(10):4419-24. doi: 10.1128/iai.62.10.4419-4424.1994.

Abstract

Since 1986, serogroup B Neisseria meningitidis has caused approximately 80% of the meningococcal disease in Brazil. In 1988, an epidemic caused by N. meningitidis B:4:P1.15 was recognized in the greater São Paulo area of Brazil. The São Paulo state government decided to vaccinate children from 3 to 83 months of age with a vaccine consisting of serotype 4 outer membrane protein and group C meningococcal polysaccharide that was produced in Cuba. About 2.7 million children were vaccinated during two immunization campaigns conducted in 1989 and 1990. Because of this, a case-control study was designed to determine vaccine efficacy against group B meningococcal disease. The purpose of our study was to compare the antibody response with the protection from disease estimated from the case-control study. We measured the immune responses of vaccinees by enzyme-linked immunosorbent assay (ELISA), immunoblot, and bactericidal assay. The development of bactericidal antibodies was age dependent and in good agreement with the results of the case-control study. Only 40% of vaccinees showed fourfold or greater increases in bactericidal antibody titers after vaccination. A poor correlation between antibody levels detected by ELISA and those by bactericidal assay was found. Immunoblot analysis showed that about 50% of the serum samples with bactericidal titers higher than 1:4 were reactive with class 1 outer membrane protein. We conclude that the bactericidal assay is a good, laboratory-based, functional assay for the study of vaccine immunogenicity and that an effective solution to group B meningococcal disease remains to be demonstrated.

摘要

自1986年以来,B群脑膜炎奈瑟菌在巴西引起了约80%的脑膜炎球菌病。1988年,巴西大圣保罗地区确认了由B:4:P1.15型脑膜炎奈瑟菌引起的疫情。圣保罗州政府决定为3至83个月大的儿童接种由古巴生产的4型外膜蛋白和C群脑膜炎球菌多糖组成的疫苗。在1989年和1990年开展的两次免疫活动中,约270万儿童接种了疫苗。因此,设计了一项病例对照研究来确定该疫苗对B群脑膜炎球菌病的效力。我们研究的目的是将抗体反应与病例对照研究估计的疾病保护情况进行比较。我们通过酶联免疫吸附测定(ELISA)、免疫印迹和杀菌试验来测量接种疫苗者的免疫反应。杀菌抗体的产生与年龄有关,并且与病例对照研究的结果高度一致。接种疫苗后,只有40%的接种者杀菌抗体滴度有四倍或更高的升高。ELISA检测的抗体水平与杀菌试验检测的抗体水平之间相关性较差。免疫印迹分析表明,杀菌滴度高于1:4的血清样本中,约50%与1类外膜蛋白发生反应。我们得出结论,杀菌试验是一种用于研究疫苗免疫原性的良好的基于实验室的功能检测方法,而针对B群脑膜炎球菌病的有效解决方案仍有待证明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5071/303125/7aff73983bac/iai00010-0335-a.jpg

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