Your browser doesn't support javascript.
loading
Effect of Leptin Receptor Q223R Polymorphism on Clostridioides difficile Infection-Induced Macrophage Migration Inhibitory Factor Production.
Mathew, Ann M; Huber, Alexander; Sous, Rowis D; Weghorn, Kristin N; Powers-Fletcher, Margaret V; Jose, Shinsmon; Madan, Rajat.
Afiliação
  • Mathew AM; Division of Infectious Diseases, University of Cincinnati College of Medicine.
  • Huber A; Pathobiology and Molecular Medicine, Department of Internal Medicine, University of Cincinnati College of Medicine.
  • Sous RD; Division of Infectious Diseases, University of Cincinnati College of Medicine.
  • Weghorn KN; Division of Immunobiology, Cincinnati Children's Hospital Medical Center.
  • Powers-Fletcher MV; Division of Infectious Diseases, University of Cincinnati College of Medicine.
  • Jose S; Division of Infectious Diseases, University of Cincinnati College of Medicine.
  • Madan R; Division of Infectious Diseases, University of Cincinnati College of Medicine.
J Infect Dis ; 2024 Apr 30.
Article em En | MEDLINE | ID: mdl-38687212
ABSTRACT
Proinflammatory cytokine levels and host genetic makeup are key determinants of Clostridioides difficile infection (CDI) outcomes. We previously reported that blocking the inflammatory cytokine macrophage migration inhibitory factor (MIF) ameliorates CDI. Here, we determined kinetics of MIF production and its association with a common genetic variant in leptin receptor (LEPR) using blood from patients with CDI. We found highest plasma MIF early after C difficile exposure and in individuals who express mutant/derived LEPR. Our data suggest that early-phase CDI provides a possible window of opportunity in which MIF targeting, potentially in combination with LEPR genotype, could have therapeutic utility.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Infect Dis Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Infect Dis Ano de publicação: 2024 Tipo de documento: Article