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Bezlotoxumab for prevention of Clostridium difficile infection recurrence: Distinguishing relapse from reinfection with whole genome sequencing.
Zeng, Zhen; Zhao, Hailong; Dorr, Mary Beth; Shen, Judong; Wilcox, Mark H; Poxton, Ian R; Guris, Dalya; Li, Junhua; Shaw, Peter M.
Afiliação
  • Zeng Z; Merck & Co., Inc., Kenilworth, NJ, USA.
  • Zhao H; BGI-Shenzhen, Shenzhen, China; China National GeneBank, BGI-Shenzhen, Shenzhen, China; Laboratory of Genomics and Molecular Biomedicine, Department of Biology, University of Copenhagen, 2100, Copenhagen Ø, Denmark.
  • Dorr MB; Merck & Co., Inc., Kenilworth, NJ, USA.
  • Shen J; Merck & Co., Inc., Kenilworth, NJ, USA.
  • Wilcox MH; Leeds Teaching Hospitals & University of Leeds, Leeds, UK.
  • Poxton IR; University of Edinburgh, Edinburgh, UK.
  • Guris D; Merck & Co., Inc., Kenilworth, NJ, USA.
  • Li J; BGI-Shenzhen, Shenzhen, China; China National GeneBank, BGI-Shenzhen, Shenzhen, China; School of Bioscience and Biotechnology, South China University of Technology, Guangzhou, China.
  • Shaw PM; Merck & Co., Inc., Kenilworth, NJ, USA. Electronic address: peter.shaw3@merck.com.
Anaerobe ; 61: 102137, 2020 Feb.
Article em En | MEDLINE | ID: mdl-31846705
ABSTRACT

BACKGROUND:

Bezlotoxumab has been shown to prevent Clostridium difficile infection recurrence (rCDI) in high-risk patients.

METHODS:

We used whole genome sequencing to estimate the impact of bezlotoxumab on same-strain relapse or new-strain reinfection in MODIFY I/II trials. Reinfection with a new strain and relapse with the same strain were differentiated by the comparison of ribotype (RT) and pair-wise single-nucleotide whole genome sequencing (WGS) variations (PWSNV). Relapse was assigned if the baseline RT and the RT isolated during rCDI were the same, and if PWSNVs were ≤ 2. Reinfection was assigned if the baseline RT and the RT isolated during rCDI were different, or if the RT was the same but PWSNVs were > 10. Unknown status was assigned if the RT was the same but PWSNVs were 3-10.

RESULTS:

259 rCDI events were evaluable (50 [19.3%] reinfection; 198 [76.4%] relapse). The proportion of relapses was higher for ribotype 027 (84.5%) compared with other ribotypes (74.1%). Cumulative incidence of relapse was significantly lower for bezlotoxumab versus no bezlotoxumab (p < 0.0001), with a non-significant trend towards reduction for reinfection (p = 0.14).

CONCLUSION:

Bezlotoxumab treatment significantly reduced the rate of CDI relapse versus a regimen without bezlotoxumab. (NCT01241552/NCT01513239).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Clostridioides difficile / Genoma Bacteriano / Infecções por Clostridium / Sequenciamento Completo do Genoma / Anticorpos Amplamente Neutralizantes / Antibacterianos / Anticorpos Monoclonais Tipo de estudo: Clinical_trials / Incidence_studies / Prognostic_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Clostridioides difficile / Genoma Bacteriano / Infecções por Clostridium / Sequenciamento Completo do Genoma / Anticorpos Amplamente Neutralizantes / Antibacterianos / Anticorpos Monoclonais Tipo de estudo: Clinical_trials / Incidence_studies / Prognostic_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article