045 Anti-IL-23 preferentially inhibits pathogenic TH17 cells

نویسندگان

چکیده

Two different TH17 subtypes were identified in the pathogenesis of Psoriasis. Non-pathogenic cells co-express IL-17 and IL-10 while pathogenic proinflammatory cytokines like IL-17, IL-22, IFN-γ TNF-α. This study aimed at defining effect IL-23 deprivation on stages cell lifecycle vitro to provide an insight into potential mechanism treatment with targeting therapies. Effector naïve T-cells up nine patients purified from human PBMC’s. neutralization was analyzed effector T-cell model a differentiation which cultured under polarizing conditions. Co-cultures autologous monocytes pulsed S. aureus C. albicans used investigate pathogen induced model. Cytokine profiles as well absolute counts by flow cytometry. In culture, IL-17/IFN-γ IL-17/IL-10 expressing decreased deprivation. decrease stronger (Δmean=-83.46 ± 9.99%) compared non-pathogenic numbers (Δmean=-35.84 50.87%). polarization monocyte co-culture models also both lower detection limit. We could demonstrate that is essential whole cells, for maintenance mature T-cells. Pathogenic more affected contrast emphasizing higher sensitivity neutralizing The selective highest cultures indicate development rather result plasticity than differentiation.

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ژورنال

عنوان ژورنال: Journal of Investigative Dermatology

سال: 2023

ISSN: ['1523-1747', '0022-202X']

DOI: https://doi.org/10.1016/j.jid.2023.03.046