Your browser doesn't support javascript.
loading
Antibodies to Toxin B Are Protective Against Clostridium difficile Infection Recurrence.
Gupta, Swati B; Mehta, Vinay; Dubberke, Erik R; Zhao, Xuemei; Dorr, Mary Beth; Guris, Dalya; Molrine, Deborah; Leney, Mark; Miller, Mark; Dupin, Marilyne; Mast, T Christopher.
Afiliación
  • Gupta SB; Public Health and Scientific Affairs.
  • Mehta V; Pharmacoepidemiology, Merck & Co, Inc, Kenilworth, New Jersey.
  • Dubberke ER; Division of Infectious Diseases, Washington University School of Medicine, St Louis, Missouri.
  • Zhao X; Translational Molecular Biomarkers.
  • Dorr MB; Clinical Research, Merck & Co, Inc, Kenilworth, New Jersey.
  • Guris D; Clinical Research, Merck & Co, Inc, Kenilworth, New Jersey.
  • Molrine D; Department of Pediatrics, University of Massachusetts Medical School, Worcester.
  • Leney M; MassBiologics, Boston.
  • Miller M; MassBiologics, Boston.
  • Dupin M; Department of Medicine, University of Massachusetts Medical School, Worcester.
  • Mast TC; Office of Medical and Scientific Affairs.
Clin Infect Dis ; 63(6): 730-734, 2016 09 15.
Article en En | MEDLINE | ID: mdl-27365387
ABSTRACT

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 metronidazole 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. CLINICAL TRIALS REGISTRATION NCT00350298.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Bacterianas / Toxinas Bacterianas / Enterocolitis Seudomembranosa / Clostridioides difficile / Anticuerpos Antibacterianos Tipo de estudio: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Bacterianas / Toxinas Bacterianas / Enterocolitis Seudomembranosa / Clostridioides difficile / Anticuerpos Antibacterianos Tipo de estudio: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2016 Tipo del documento: Article