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dc.contributor.authorGupta, Swati B.
dc.contributor.authorMehta, Vinay
dc.contributor.authorDubberke, Erik R.
dc.contributor.authorZhao, Xuemei
dc.contributor.authorDorr, Mary Beth
dc.contributor.authorGuris, Dalya
dc.contributor.authorMolrine, Deborah C.
dc.contributor.authorLeney, Mark
dc.contributor.authorMiller, Mark
dc.contributor.authorDupin, Marilyne
dc.contributor.authorMast, T. Christopher
dc.date2022-08-11T08:10:14.000
dc.date.accessioned2022-08-23T17:00:22Z
dc.date.available2022-08-23T17:00:22Z
dc.date.issued2016-09-15
dc.date.submitted2016-11-16
dc.identifier.citationClin Infect Dis. 2016 Sep 15;63(6):730-4. doi: 10.1093/cid/ciw364. Epub 2016 Jun 30. <a href="http://dx.doi.org/10.1093/cid/ciw364">Link to article on publisher's site</a>
dc.identifier.issn1058-4838 (Linking)
dc.identifier.doi10.1093/cid/ciw364
dc.identifier.pmid27365387
dc.identifier.urihttp://hdl.handle.net/20.500.14038/43782
dc.description.abstractBACKGROUND: 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.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=27365387&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1093/cid/ciw364
dc.subjectantibodies
dc.subjectepidemiology
dc.subjectrisk factors
dc.subjectserology
dc.subjecttoxin A
dc.subjectBacterial Infections and Mycoses
dc.subjectImmunology and Infectious Disease
dc.subjectInfectious Disease
dc.titleAntibodies to Toxin B Are Protective Against Clostridium difficile Infection Recurrence
dc.typeJournal Article
dc.source.journaltitleClinical infectious diseases : an official publication of the Infectious Diseases Society of America
dc.source.volume63
dc.source.issue6
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/peds_pp/92
dc.identifier.contextkey9383594
html.description.abstract<p>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.</p> <p>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.</p> <p>RESULTS: A predictor of recurrence was age > /=65 years, and an antibody-mediated immune response to toxin B appears to be protective against rCDI.</p> <p>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.</p> <p>CLINICAL TRIALS REGISTRATION: NCT00350298.</p>
dc.identifier.submissionpathpeds_pp/92
dc.contributor.departmentDepartment of Medicine
dc.contributor.departmentMassBiologics
dc.contributor.departmentDepartment of Pediatrics, Division of Immunology/Infectious Disease
dc.source.pages730-4


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