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
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
相关论文
共 22 条
[1]   RISK OF PNEUMOCOCCAL DISEASE IN INDIVIDUALS WITHOUT A SPLEEN [J].
AAVITSLAND, P ;
FROHOLM, LO ;
HOIBY, EA ;
LYSTAD, A .
LANCET, 1994, 344 (8935) :1504-1504
[2]   Risk of infection and death among post-splenectomy patients [J].
Bisharat, N ;
Omari, H ;
Lavi, I ;
Raz, R .
JOURNAL OF INFECTION, 2001, 43 (03) :182-186
[3]  
*CDCP, 1997, MMWR-MORBID MORTAL W, V46, P1
[4]   SEVERE LATE POSTSPLENECTOMY INFECTION [J].
CULLINGFORD, GL ;
WATKINS, DN ;
WATTS, ADJ ;
MALLON, DF .
BRITISH JOURNAL OF SURGERY, 1991, 78 (06) :716-721
[5]  
Ejstrud P, 2000, SCAND J INFECT DIS, V32, P521, DOI 10.1080/003655400458811
[6]  
ESKOLA J, 2003, VACCINES
[7]  
FEDSON DS, 2003, VACCINES
[8]   VACCINE-TYPE PNEUMOCOCCAL PNEUMONIA - OCCURRENCE AFTER VACCINATION IN AN ASPLENIC PATIENT [J].
GIEBINK, GS ;
SCHIFFMAN, G ;
KRIVIT, W ;
QUIE, PG .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1979, 241 (25) :2736-2737
[9]  
HERER B, 1986, NOUV REV FR HEMATOL, V28, P371
[10]   PNEUMOCOCCAL INFECTIONS IN SPLENECTOMIZED CHILDREN ARE PREVENTABLE [J].
KONRADSEN, HB ;
HENRICHSEN, J .
ACTA PAEDIATRICA SCANDINAVICA, 1991, 80 (04) :423-427