POLYSACCHARIDE CONJUGATE VACCINE RESPONSES IN BONE-MARROW TRANSPLANT PATIENTS

被引:95
作者
GUINAN, EC
MOLRINE, DC
ANTIN, JH
LEE, MC
WEINSTEIN, HJ
SALLAN, SE
PARSONS, SK
WHEELER, C
GROSS, W
MCGARIGLE, C
BLANDING, P
SCHIFFMAN, G
FINBERG, RW
SIBER, GR
BOLON, D
WANG, M
CARIATI, S
AMBROSINO, DM
机构
[1] DANA FABER CANC INST,DEPT PEDIAT ONCOL,INFECT DIS LAB,BOSTON,MA 02115
[2] DANA FABER CANC INST,DEPT PHARM,BOSTON,MA 02115
[3] BRIGHAM & WOMENS HOSP,CHILDRENS HOSP,DIV HEMATOL,BOSTON,MA 02115
[4] BRIGHAM & WOMENS HOSP,CHILDRENS HOSP,DIV ONCOL,BOSTON,MA 02115
[5] BETH ISRAEL HOSP,BOSTON,MA 02115
[6] SUNY HLTH SCI CTR,DEPT MICROBIOL & IMMUNOL,BROOKLYN,NY 11203
关键词
D O I
10.1097/00007890-199403150-00009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Bone marrow transplant patients have impaired responses to pure polysaccharide (PS) vaccines and are at an increased risk for disease caused by PS encapsulated pathogens such as Haemophilus influenzae type B (HIB) and Streptococcus pneumoniae. We immunized 35 BMT patients (21 allogeneic and 14 autologous) ages 2-45 years with pure PS pneumococcal (Pnu-imune 23), HIB-conjugate (HibTITER), and tetanus toroid vaccines. Patients were assigned to receive vaccines at either 12 and 24 months after transplantation or at 24 months only. Only 19% of all enrolled patients developed protective antibody concentrations (greater than or equal to 0.300 mu g antibody nitrogen/ml) to the 6 pneumococcal serotypes measured after the 24-month immunization. Poor response to pneumococcal vaccine was not different for the 2 study groups and was similar to previous studies. In contrast, HIB-coqjugate vaccine elicited protective concentrations of antibody (greater than or equal to 1.0 mu g/ml) in 56% of patients after 1 dose and in 80% after 2 doses. The group that received 2 doses of HIB-conjugate vaccine had a significantly higher geometric mean antibody concentration of 14.5 mu g/ml as compared with 1.43 mu g/ml for those receiving only 1 dose (P=0.012). Responses to tetanus toroid vaccine were similar to HIB-conjugate vaccine, with a booster response documented after the second dose. In summary 2 doses of HIB-coqjugate vaccine given at 12 and 24 months after transplantation produced protective antibody concentrations in 80% of patients. While the response to pure PS pneumococcal vaccine was poor, the results with HIB-coqjugate vaccine suggest that future pneumococcal conjugate vaccines may also benefit BMT patients.
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收藏
页码:677 / 684
页数:8
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