Chronic helminth infections impair pneumococcal vaccine responses

被引:19
作者
Apiwattanakul, Nopporn [1 ]
Thomas, Paul G. [2 ]
Iverson, Amy R. [1 ]
McCullers, Jonathan A. [1 ,3 ]
机构
[1] St Jude Childrens Res Hosp, Dept Infect Dis, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38105 USA
[3] Univ Tennessee, Hlth Sci Ctr, Dept Pediat, Memphis, TN 38103 USA
关键词
Helminths; Streptococcus pneumoniae; Pneumonia; Pneumococcal vaccine; Prevnar; Pneumovax; CONJUGATE VACCINE; STREPTOCOCCUS-PNEUMONIAE; INFLUENZA-VIRUS; RESEARCH AGENDA; DOUBLE-BLIND; EFFICACY; BCG; IMMUNOGENICITY; CHILDREN; DISEASE;
D O I
10.1016/j.vaccine.2014.07.107
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Pneumonia is the leading killer of children and disproportionately affects developing countries. Vaccination campaigns against Streptococcus pneumoniae, the leading cause of pneumonia, have recently been launched with a new conjugate vaccine in Africa. Using a mouse model, we assessed the potential role that the high burden of helminth infections in the countries targeted for vaccine might have on vaccine effectiveness. Mice vaccinated with either commercial conjugate or purified polysaccharide vaccines had impaired antibody responses if they were chronically infected with Taenia crassiceps. This translated to increased susceptibility to pneumococcal pneumonia and high mortality compared to helminth-negative vaccinated animals, which were fully protected from disease and death. Antibodies taken from Taenia-infected, vaccinated mice were unable to effectively opsonize S. pneumoniae for killing by alveolar macrophages, and did not protect against pneumococcal challenge when adoptively transferred into naive animals. These data may have implications for vaccination programs in countries endemic with helminths. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5405 / 5410
页数:6
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