The 23-valent pneumococcal polysaccharide vaccine does not provide additional serotype antibody protection in children who have been primed with two doses of heptavalent pneumococcal conjugate vaccine

被引:17
作者
Balmer, Paul
Orrow, Ray B.
Arkwright, Peter D.
机构
[1] Univ Manchester, Booth Hall Childrens Hosp, Manchester M9 7AA, Lancs, England
[2] Manchester Royal Infirm, Clin Sci Bldg 2, Hlth Protect Agcy, Manchester M13 9WL, Lancs, England
关键词
Streptococcus pneumoniae; pneumococcal antibodies; serotypes; vaccine; children;
D O I
10.1016/j.vaccine.2007.06.021
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Current guidelines recommend up to two doses of the pneumococcal conjugate heptavalent vaccine (PCV-7) in children up to 5 years old followed by and a dose of the polysaccharide vaccine (PPV-23) for patients over 2 years old to broaden serotype immunity. We assessed the serotype responses to two doses of PCV-7 and a dose of PPV-23 in a cohort of children in the 2-16-year age range in order to determine whether PPV-23 induced effective immunity to non-PCV-7 serotypes. Pneumococcal antibody concentrations to the seven serotypes covered by PCV-7 and five additional serotypes covered by PPV-23 but not PCV-7 were measured in 60 children aged 2-16 years. None of the children had a primary antibody immunodeficiency. Vaccinated children had 7-30-fold higher antibody concentrations than unvaccinated children to all serotypes contained in the PCV-7 (P<0.001). In contrast, serotypes covered by the PPV-23 but not PCV-7 were only one- to two-fold higher and there was no significant increase in the number of children who had protective concentrations of antibody ( >= 0.35 mcg/ml) against these serotypes. In this cohort of children, PPV-23 vaccine did not broaden the protection in vitro against potentially pathogenic strains of Streptococcus pneumoniae. We call into question the recommendation to use the PPV-23 in children. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6321 / 6325
页数:5
相关论文
共 22 条
[11]   Development and validation of a nonaplex assay for the simultaneous quantitation of antibodies to nine Streptococcus pneumoniae serotypes [J].
Lal, G ;
Balmer, P ;
Stanford, E ;
Martin, S ;
Warrington, R ;
Borrow, R .
JOURNAL OF IMMUNOLOGICAL METHODS, 2005, 296 (1-2) :135-147
[12]   Efficacy of polysaccharide pneumococcal vaccine in adults in more developed countries: the state of the evidence [J].
Mangtani, P ;
Cutts, F ;
Hall, AJ .
LANCET INFECTIOUS DISEASES, 2003, 3 (02) :71-78
[13]   The 23-valent pneumococcal polysaccharide vaccine. Part I. Efficacy of PPV in the elderly: A comparison of meta-analyses [J].
Melegaro A. ;
Edmunds W.J. .
European Journal of Epidemiology, 2004, 19 (4) :353-363
[14]   Administration of protein-conjugate pneumococcal vaccine to patients who have invasive disease after splenectomy despite their having received 23-valent pneumococcal polysaccharide vaccine [J].
Musher, DM ;
Ceasar, H ;
Kojic, EM ;
Musher, BL ;
Gathe, JC ;
Romero-Steiner, S ;
White, AC .
JOURNAL OF INFECTIOUS DISEASES, 2005, 191 (07) :1063-1067
[15]  
SALBURY D, 2006, DEP HLTH UK TSO 2006
[16]   ELISA IgG concentrations and opsonophagocytic activity following pneumococcal protein D conjugate vaccination and relationship to efficacy against acute otitis media [J].
Schuerman, Lode ;
Prymula, Roman ;
Henckaerts, Isabelle ;
Poolman, Jan .
VACCINE, 2007, 25 (11) :1962-1968
[17]  
SCOTT DA, 2006, P 5 INT S PNEUM PNEU
[18]  
SIBER GR, 2007, VACCINE 0221
[19]   Effects of prior polysaccharide vaccination on magnitude, duration, and quality of immune responses to and safety profile of a meningococcal serogroup C tetanus toxoid conjugate vaccination in adults [J].
Southern, J ;
Deane, S ;
Ashton, L ;
Borrow, R ;
Goldblatt, D ;
Andrews, N ;
Balmer, P ;
Morris, R ;
Kroll, JS ;
Miller, E .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2004, 11 (06) :1100-1104
[20]   Streptococcus pneumoniae protein vaccine candidates:: Properties, activities and animal studies [J].
Tai, Stanley S. .
CRITICAL REVIEWS IN MICROBIOLOGY, 2006, 32 (03) :139-153