Are anticapsular antibodies the primary mechanism of protection against invasive pneumococcal disease?

被引:106
作者
Lipsitch, M [1 ]
Whitney, CG
Zell, E
Kaijalainen, T
Dagan, R
Malley, R
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[3] Natl Ctr Infect Dis, Act Bacterial Core Suveillance, Atlanta, GA USA
[4] Natl Ctr Infect Dis, Div Bacterial & Mycot Dis, Ctr Dis Control & Prevent, Atlanta, GA USA
[5] Natl Publ Hlth Inst, Natl Reference Lab Pneumococcus, Oulu, Finland
[6] Ben Gurion Univ Negev, Fac Hlth Sci, IL-84105 Beer Sheva, Israel
[7] Soroka Univ, Med Ctr, Pediat Infect Dis Unit, Beer Sheva, Israel
[8] Childrens Hosp, Boston, MA 02115 USA
[9] Harvard Univ, Sch Med, Boston, MA 02115 USA
来源
PLOS MEDICINE | 2005年 / 2卷 / 01期
关键词
D O I
10.1371/journal.pmed.0020015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Antibody to capsular polysaccharide has been the basis of several vaccines that offer protection against invasive disease from Streptococcus pneumoniae. The success of such vaccines has led to the inference that natural protection against invasive pneumococcal disease is largely conferred by anticapsular antibody. If this is so, one would expect that the decline in disease from different serotypes would vary significantly, and that the appearance of substantial concentrations of anticapsular antibodies would coincide temporally with the decline in age-specific incidence. Methods and Findings,Using incidence data from the United States, we show that, on the contrary, the decline in incidence with age is quite similar for the seven most important serogroups, despite large differences in exposure in the population. Moreover, only modest increases in antibody concentration occur over the second and third years of life, a period in which serotype-specific incidence declines to less than 25% of its peak. We also present detailed data on the distribution of antibody concentrations in Israeli toddlers, which are consistent with the United States findings. The same conclusion is supported by new data on age-specific incidence in Finland, which is compared with published data on antibody acquisition in Finnish toddlers. Conclusion We suggest some additional studies of the mechanisms of protection that could distinguish among potential alternative mechanisms, including acquired immunity to noncapsular antigens, maturation of nonspecific immune responses, or changes in anatomy or exposure.
引用
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页码:62 / 68
页数:7
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