PLoS ONE (Jan 2022)

Association between ustekinumab therapy and changes in specific anti-microbial response, serum biomarkers, and microbiota composition in patients with IBD: A pilot study.

  • Filip Rob,
  • Dagmar Schierova,
  • Zuzana Stehlikova,
  • Jakub Kreisinger,
  • Radka Roubalova,
  • Stepan Coufal,
  • Martin Mihula,
  • Zuzana Jackova,
  • Miloslav Kverka,
  • Tomas Thon,
  • Klara Kostovcikova,
  • Lukas Bajer,
  • Pavel Drastich,
  • Jana Tresnak Hercogova,
  • Michaela Novakova,
  • Martin Kolar,
  • Martin Vasatko,
  • Milan Lukas,
  • Helena Tlaskalova-Hogenova,
  • Zuzana Jiraskova Zakostelska

DOI
https://doi.org/10.1371/journal.pone.0277576
Journal volume & issue
Vol. 17, no. 12
p. e0277576

Abstract

Read online

BackgroundUstekinumab, is a new therapy for patients with IBD, especially for patients suffering from Crohn's disease (CD) who did not respond to anti-TNF treatment. To shed light on the longitudinal effect of ustekinumab on the immune system, we investigated the effect on skin and gut microbiota composition, specific immune response to commensals, and various serum biomarkers.Methodology/principal findingsWe recruited 11 patients with IBD who were monitored over 40 weeks of ustekinumab therapy and 39 healthy controls (HC). We found differences in the concentrations of serum levels of osteoprotegerin, TGF-β1, IL-33, and serum IgM antibodies against Lactobacillus plantarum between patients with IBD and HC. The levels of these biomarkers did not change in response to ustekinumab treatment or with disease improvement during the 40 weeks of observation. Additionally, we identified differences in stool abundance of uncultured Subdoligranulum, Faecalibacterium, and Bacteroides between patients with IBD and HC.Conclusion/significanceIn this preliminary study, we provide a unique overview of the longitudinal monitoring of fecal and skin microbial profiles as well as various serum biomarkers and humoral and cellular response to gut commensals in a small cohort of patients with IBD on ustekinumab therapy.