1. Academic Validation
  2. Cysteinyl Leukotrienes in Allergic Inflammation

Cysteinyl Leukotrienes in Allergic Inflammation

  • Annu Rev Pathol. 2025 Jan;20(1):115-141. doi: 10.1146/annurev-pathmechdis-111523-023509.
Minkyu Lee 1 2 Joshua A Boyce 1 2 Nora A Barrett 1 2
Affiliations

Affiliations

  • 1 Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
  • 2 Jeff and Penny Vinik Center for Translational Immunology Research, Division of Allergy and Clinical Immunology, Brigham and Women's Hospital, Boston, Massachusetts, USA; email: [email protected], [email protected], [email protected].
Abstract

The cysteinyl leukotrienes (CysLTs), LTC4, LTD4, and LTE4, are potent lipid mediators derived from arachidonic acid through the 5-lipoxygenase pathway. These mediators produce both inflammation and bronchoconstriction through three distinct G protein-coupled receptors (GPCRs)-CysLT1, CysLT2, and OXGR1 (also known as CysLT3 or GPR99). While CysLT-mediated functions in the effector phase of allergic inflammation and asthma have been established for some time, recent work has demonstrated novel roles for these mediators and their receptors in the induction and amplification of type 2 inflammation. Additionally, in vitro studies and murine models have uncovered diverse regulatory mechanisms that restrain or amplify CysLT receptor activation and CysLT receptor function. This review provides an overview of CysLT biosynthesis and its regulation, the molecular and functional pharmacology of CysLT receptors, and an overview of the established and emerging roles of CysLTs in asthma, aspirin-exacerbated respiratory disease, and type 2 inflammation.

Keywords

airway remodeling; allergic inflammation; aspirin-exacerbated respiratory disease; asthma; cysteinyl leukotriene.

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