Antibodies to Toxin B Are Protective Against Clostridium difficile Infection Recurrence

被引:59
作者
Gupta, Swati B. [1 ]
Mehta, Vinay [2 ]
Dubberke, Erik R. [3 ]
Zhao, Xuemei [4 ]
Dorr, Mary Beth [5 ]
Guris, Dalya [5 ]
Molrine, Deborah [6 ,7 ]
Leney, Mark [7 ,8 ]
Miller, Mark [9 ]
Dupin, Marilyne [10 ]
Mast, T. Christopher [2 ]
机构
[1] Merck & Co Inc, Publ Hlth & Sci Affairs, Kenilworth, NJ USA
[2] Merck & Co Inc, Pharmacoepidemiol, Kenilworth, NJ USA
[3] Washington Univ, Sch Med, Div Infect Dis, St Louis, MO 63110 USA
[4] Merck & Co Inc, Translat Mol Biomarkers, Kenilworth, NJ USA
[5] Merck & Co Inc, Clin Res, Kenilworth, NJ USA
[6] Univ Massachusetts, Sch Med, Dept Pediat, Worcester, MA USA
[7] MassBiologics, Boston, MA USA
[8] Univ Massachusetts, Sch Med, Dept Med, Worcester, MA USA
[9] BioMerieux, Off Med & Sci Affairs, Marcy Letoile, France
[10] BioMerieux, Med Diagnost Discovery Dept, Marcy Letoile, France
关键词
epidemiology; risk factors; antibodies; toxin A; serology; RISK-PREDICTION MODEL; DIARRHEA; DISEASE; BURDEN; VALIDATION; RATES;
D O I
10.1093/cid/ciw364
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Although newer studies have evaluated risk factors for recurrent Clostridium difficile infection (CDI), the vast majority did not measure important biomarkers such as endogenous anti-toxin A and anti-toxin B antibody levels. Methods. Data from the placebo group of a phase 2 trial testing monoclonal antibodies to C. difficile toxins A and B for preventing CDI recurrence (rCDI) were analyzed to assess risk factors associated with rCDI. Patients with symptomatic CDI taking etronidazole or vancomycin were enrolled. The primary outcome was rCDI within 84 days of treatment start. Univariate and multivariate logistic regression was used to examine associations between potential risk factors and rCDI. At baseline, demographic and clinical characteristics were recorded; endogenous antibody levels were assessed using 2 enzyme-linked immunosorbent assays. Results. A predictor of recurrence was age >= 65 years, and an antibody-mediated immune response to toxin B appears to be protective against rCDI. Conclusions. Our findings demonstrate the importance of clinical as well as immunological risk factors in rCDI and provide more robust evidence for the protective effects of antibody to toxin B in the prevention of rCDI.
引用
收藏
页码:730 / 734
页数:5
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