Use of a Staphylococcus aureus conjugate vaccine in patients receiving hemodialysis.

被引:341
|
作者
Shinefield, H
Black, S
Fattom, A
Horwith, G
Rasgon, S
Ordonez, J
Yeoh, H
Law, D
Robbins, JB
Schneerson, R
Muenz, L
Naso, R
机构
[1] Kaiser Permanente Vaccine Study Ctr, Oakland, CA 94612 USA
[2] Nabi, Rockville, MD USA
[3] So Calif Kaiser Permanente, Los Angeles, CA USA
[4] NICHHD, Bethesda, MD 20892 USA
[5] Larry Muenz & Associates, Rockville, MD USA
[6] Total Renal Res, Minneapolis, MN USA
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2002年 / 346卷 / 07期
关键词
D O I
10.1056/NEJMoa011297
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: In patients with decreased resistance to infection, Staphylococcus aureus is a major cause of bacteremia and its complications. The capsular polysaccharides are essential for the pathogenesis of and immunity to S. aureus infection and are targets for vaccines. Methods: In a double-blind trial involving patients with end-stage renal disease who were receiving hemodialysis, we evaluated the safety, immunogenicity, and efficacy of a vaccine with S. aureus type 5 and 8 capsular polysaccharides conjugated to nontoxic recombinant Pseudomonas aeruginosa exotoxin A. Between April 1998 and August 1999, 1804 adult patients at 73 hemodialysis centers were randomly assigned to receive a single intramuscular injection of either vaccine or saline. IgG antibodies to S. aureus type 5 and 8 capsular polysaccharides were measured for up to two years, and episodes of S. aureus bacteremia were recorded. Efficacy was estimated by comparing the incidence of S. aureus bacteremia in the patients who received the vaccine with the incidence in the control patients. Results: Reactions to the vaccine were generally mild to moderate, and most resolved within two days. The capsular polysaccharides elicited an antibody response of at least 80 microg per milliliter (the estimated minimal level conferring protection) in 80 percent of patients for type 5 and in 75 percent of patients for type 8. The efficacy during weeks 3 to 54 was only 26 percent (P=0.23). However, between weeks 3 and 40 after vaccination, S. aureus bacteremia developed in 11 of 892 patients in the vaccine group who could be evaluated for bacteremia, as compared with 26 of 906 patients in the control group (estimate of efficacy, 57 percent; 95 percent confidence interval, 10 to 81 percent; nominal P=0.02). Conclusions: In patients receiving hemodialysis, a conjugate vaccine can confer partial immunity against S. aureus bacteremia for approximately 40 weeks, after which protection wanes as antibody levels decrease. (N Engl J Med 2002;346:491-6.) Copyright (C) 2002 Massachusetts Medical Society.
引用
收藏
页码:491 / 496
页数:6
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