Immunopathogenesis of ocular allergy: a schematic approach to different clinical entities

Curr Opin Allergy Clin Immunol. 2007 Oct;7(5):429-35. doi: 10.1097/ACI.0b013e3282ef8674.

Abstract

Purpose of review: The immunopathogenesis of ocular allergic disorders is generally related to the specific immunoglobulin E-mediated mast cell activation and the following cascade of inflammatory mediators. Seasonal and perennial allergic conjunctivitis, however, are the only ocular diseases to involve solely type I hypersensitivity. The other main forms, vernal and atopic keratoconjunctivitis, have a more complex immunological basis and a chronic inflammatory component. Involvement of inflammatory cells, particularly eosinophils and T cells, cytokines and proteases can lead to more serious corneal damage with vision-threatening potential.

Recent findings: Experimental allergic conjunctival models and clinical research studies have shown that T helper type 2-related mechanisms are definitely involved in the sensitization phase of ocular allergy, however, both T helper type 1 and type 2 cytokines are overexpressed in the active disease, contributing to the development of ocular inflammation.

Summary: A review of the recent literature allows us to better understand the mechanisms involved in the development of ocular allergy and to guide us toward a more schematic approach, which could possibly be useful in forming a new classification, standardizing clinical phases and individuating new treatment targets.

Publication types

  • Review

MeSH terms

  • Animals
  • Conjunctivitis, Allergic* / immunology
  • Conjunctivitis, Allergic* / metabolism
  • Conjunctivitis, Allergic* / physiopathology
  • Cytokines / immunology*
  • Cytokines / metabolism
  • Eosinophils / immunology
  • Eosinophils / metabolism
  • Eye / immunology
  • Humans
  • Immunoglobulin E / immunology*
  • Inflammation Mediators / immunology
  • Inflammation Mediators / metabolism
  • Keratoconjunctivitis* / immunology
  • Keratoconjunctivitis* / metabolism
  • Keratoconjunctivitis* / physiopathology
  • Mast Cells / immunology
  • Mast Cells / metabolism
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism

Substances

  • Cytokines
  • Inflammation Mediators
  • Immunoglobulin E