Administration of protein-conjugate pneumococcal vaccine to patients who have invasive disease after splenectomy despite their having received 23-valent pneumococcal polysaccharide vaccine

被引:29
|
作者
Musher, DM
Ceasar, H
Kojic, EM
Musher, BL
Gathe, JC
Romero-Steiner, S
White, AC
机构
[1] Michael E DeBakey Vet Affairs Med Ctr, Infect Dis Sect, Houston, TX USA
[2] Ben Taub Gen Hosp, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Med, Houston, TX 77030 USA
[4] Baylor Coll Med, Dept Mol Virol & Microbiol, Houston, TX 77030 USA
[5] Ctr Dis Control & Prevent, Atlanta, GA USA
来源
JOURNAL OF INFECTIOUS DISEASES | 2005年 / 191卷 / 07期
关键词
D O I
10.1086/428135
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Patients who undergo splenectomy are at greatly increased risk for overwhelming pneumococcal bacteremia and death. Twenty-three-valent pneumococcal polysaccharide vaccine ( PPV- 23), which contains capsular polysaccharides (PSs) from 23 common serotypes of Streptococcus pneumoniae, is strongly recommended for such patients. The capacity to respond to PPV- 23 by producing immunoglobulin (Ig) G is genetically regulated. Some proportion of adults do not respond and, despite postsplenectomy administration of PPV- 23, may remain susceptible to recurrent pneumococcal sepsis. Here, we describe 2 patients who had recurring pneumococcal bacteremia after undergoing splenectomy despite having received numerous doses of PPV- 23. Heptavalent protein-conjugate pneumococcal vaccine (PCPV-7) was then administered, and it induced high levels of IgG to all 7 PSs; in one of the patients, functional activity against 5 of the 7 PSs was demonstrable, both in vitro and in vivo. Recurrent pneumococcal bacteremia in patients who have undergone splenectomy may indicate a genetically regulated failure to respond to PPV- 23; PCPV-7 may stimulate production of IgG to PSs in such patients.
引用
收藏
页码:1063 / 1067
页数:5
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