Haemophilus influenzae type b vaccine failure in children is associated with inadequate production of high-quality antibody

被引:57
作者
Lee, Yeh Chen [1 ]
Kelly, Dominic F. [1 ]
Yu, Ly-Mee [2 ]
Slack, Mary P. E. [3 ]
Booy, Robert [5 ]
Heath, Paul T. [4 ]
Siegrist, Claire-Anne [6 ,7 ]
Moxon, Richard E. [1 ]
Pollard, Andrew J. [1 ]
机构
[1] Univ Oxford, Univ Dept Paediat, Oxford, England
[2] Ctr Stat Med, Oxford, England
[3] Hlth Protect Agcy Ctr Infect, Resp & Syst Infect Lab, Haemophilus Reference Unit, London, England
[4] Univ London, St Georges, Div Child Hlth, London, England
[5] Natl Ctr Immunisat Res & Surveillance, Sydney, NSW, Australia
[6] Univ Geneva, Sch Med, World Hlth Org Collaborating Ctr Neonatal Vaccino, Dept Pathol, CH-1211 Geneva, Switzerland
[7] Univ Geneva, Sch Med, Dept Pediat, CH-1211 Geneva, Switzerland
关键词
D O I
10.1086/524668
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Despite the excellent immunogenicity of Haemophilus influenzae type b (Hib) conjugate vaccines, breakthrough cases of Hib disease still affect a small proportion of vaccinated children in the United Kingdom. We performed a retrospective study to compare the avidity of antibody directed against the Hib polysaccharide capsule (PRP) in children who experienced Hib vaccine failure in the United Kingdom among 3 historical cohorts and with age-matched healthy control subjects. Methods. Serum samples from vaccinated children with invasive Hib disease were collected beginning in 1992 as part of enhanced surveillance for Hib disease following vaccine introduction. A total of 251 children who experienced Hib vaccine failure were identified from 3 historical cohorts (1992-1995, 1996-1999, and 2000-2003). The anti-PRP antibody concentration and avidity from healthy age-matched control subjects was obtained for the 3 contemporary time points (1995, 1999, and 2002). Serum anti-PRP antibody concentration was measured in each of the samples using a standard Hib ELISA, and antibody avidity was determined using thiocyanate elution. Results. Within the first 60 days after disease onset, there was no change in the anti-PRP antibody avidity, and there was no statistically significant difference in the geometric mean Hib antibody avidity over the 3 study periods. However, the children who experienced Hib vaccine failure had significantly lower Hib antibody avidity than did healthy control subjects, despite a marked antibody response following infection. Conclusions. Children who experience Hib disease despite vaccination appear to have a defect in immunological priming, leading to a qualitative difference in Hib-specific memory B cells. Low anti-PRP antibody avidity decreases the functional activity of anti-PRP antibody in the sera of these children experiencing vaccine failure, leading to disease susceptibility.
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收藏
页码:186 / 192
页数:7
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