Your browser doesn't support javascript.
loading
Immunomodulating effects of the single bacterial strain therapy EDP1815 on innate and adaptive immune challenge responses - a randomized, placebo-controlled clinical trial.
Eveleens Maarse, Boukje C; Ronner, Micha N; Jansen, Manon A A; Niemeyer-van der Kolk, Tessa; In 't Veld, Aliede E; Klaassen, Erica S; Ahmad, Saira; Itano, Andrea; McHale, Duncan; Moerland, Matthijs.
Afiliação
  • Eveleens Maarse BC; Centre for Human Drug Research, Zernikedreef 8, 2333 CL, Leiden, The Netherlands.
  • Ronner MN; Leiden University Medical Centre, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
  • Jansen MAA; Centre for Human Drug Research, Zernikedreef 8, 2333 CL, Leiden, The Netherlands.
  • Niemeyer-van der Kolk T; Leiden University Medical Centre, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
  • In 't Veld AE; Centre for Human Drug Research, Zernikedreef 8, 2333 CL, Leiden, The Netherlands.
  • Klaassen ES; Centre for Human Drug Research, Zernikedreef 8, 2333 CL, Leiden, The Netherlands.
  • Ahmad S; Leiden University Medical Centre, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
  • Itano A; Centre for Human Drug Research, Zernikedreef 8, 2333 CL, Leiden, The Netherlands.
  • McHale D; Leiden University Medical Centre, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
  • Moerland M; Centre for Human Drug Research, Zernikedreef 8, 2333 CL, Leiden, The Netherlands.
Immunol Res ; 72(4): 776-787, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38748319
ABSTRACT
The gut microbiome can modulate systemic inflammation and is therefore target for immunomodulation. Immunomodulating effects of EDP1815, a bacterial commensal strain of Prevotella histicola, were studied in healthy participants. Effects on adaptive immunity were evaluated by a neo-antigen challenge with keyhole limpet haemocyanin (KLH), while effects on innate immunity were evaluated by topical toll-like receptor 7 (TLR7) agonist imiquimod. Capsules with two enteric coating levels (EC1, EC2) were compared. Thirty-six healthy participants were included and received a daily dose of 8 × 1010 cells EDP1815-EC1, EDP1815-EC2 or placebo (randomization 111) for 60 days. They received KLH vaccinations at days 8, 24 and 36, with intradermal skin challenge at day 57. KLH challenge outcomes were antibody levels, and skin blood flow and erythema after skin challenge, measured by imaging techniques. Imiquimod administration started at day 57, for 72 h. Outcomes consisted of imaging measurements similar to the KLH challenge, and the influx of inflammatory cells and cytokines in blister fluid. There was no effect of EDP1815 treatment on the KLH challenge, neither on the imaging outcomes of the imiquimod challenge. There was a consistently lower influx of inflammatory cells in the blister fluid of EDP1815-treated participants (neutrophils, p = 0.016; granulocytes, p = 0.024), more pronounced in EC1. There was a lower influx of interleukin [IL]-1ß, IL-6, IL-8, IL-10, interferon [IFN]-γ and tumour necrosis factor in blister fluid of EDP1815-treated participants. EDP1815 had immunomodulatory effects on the innate immune response driven by imiquimod, but no effect on the KLH challenge was observed. Trial registration number NCT05682222; date 22 July 2022.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Imunidade Adaptativa / Imiquimode / Imunidade Inata Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Imunidade Adaptativa / Imiquimode / Imunidade Inata Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article