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DOI 10.1056/nejmoa011297

Медицинская библиотека · The New England journal of medicine · 2002

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

Shinefield Henry, Black Steven, Fattom Ali, Horwith Gary, Rasgon Scott, Ordonez Juan, Yeoh Hock, Law David, Robbins John B, Schneerson Rachel, Muenz Larry, Fuller Steve, Johnson Joanie, Fireman Bruce, Alcorn Harry, Naso Robert

Клиническое исследованиеСтатьяМногоцентровое исследованиеРандомизированное исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

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.

Для цитирования: Shinefield Henry, Black Steven, Fattom Ali, Horwith Gary, Rasgon Scott, Ordonez Juan, Yeoh Hock, Law David, Robbins John B, Schneerson Rachel, Muenz Larry, Fuller Steve, Johnson Joanie, Fireman Bruce, Alcorn Harry, Naso Robert. Use of a Staphylococcus aureus conjugate vaccine in patients receiving hemodialysis.. The New England journal of medicine. 2002. DOI: 10.1056/nejmoa011297.

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