AI Article Synopsis

  • The OX40 receptor and its ligand, OX40L, are key regulators of the adaptive immune response, particularly influencing T cell activity which is essential in skin disorders like atopic dermatitis (AD).
  • T helper 2 (T2) cells, which are activated by the OX40-OX40L interaction, produce cytokines that lead to skin inflammation and symptoms such as itchiness in AD patients.
  • Emerging therapies that target the OX40-OX40L pathway show promise for treating moderate-to-severe AD, indicating a potential new direction for managing this condition.

Article Abstract

The transmembrane glycoprotein OX40 receptor (OX40) and its ligand, OX40L, are instrumental modulators of the adaptive immune response in humans. OX40 functions as a costimulatory molecule that promotes T cell activation, differentiation, and survival through ligation with OX40L. T cells play an integral role in the pathogenesis of several inflammatory skin conditions, including atopic dermatitis (AD). In particular, T helper 2 (T2) cells strongly contribute to AD pathogenesis via the production of cytokines associated with type 2 inflammation (e.g., IL-4, IL-5, IL-13, and IL-31) that lead to skin barrier dysfunction and pruritus. The OX40-OX40L interaction also promotes the activation and proliferation of other T helper cell populations (e.g., T1, T22, and T17), and AD patients have demonstrated higher levels of OX40 expression on peripheral blood mononuclear cells than healthy controls. As such, the OX40-OX40L pathway is a potential target for AD treatment. Novel therapies targeting the OX40 pathway are currently in development, several of which have demonstrated promising safety and efficacy results in patients with moderate-to-severe AD. Herein, we review the function of OX40 and the OX40-OX40L signaling pathway, their role in AD pathogenesis, and emerging therapies targeting OX40-OX40L that may offer insights into the future of AD management.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11011471PMC
http://dx.doi.org/10.3390/cells13070587DOI Listing

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