Gut-licensed β7+ CD4+ T cells contribute to progressive retinal ganglion cell damage in glaucoma 2023, Chong He et al

[Sly Saint]

Editor’s summary
T cells are likely involved in glaucoma pathogenesis, but how they gain retinal access remains elusive. He and colleagues discovered an association of CD4+ T cells that express the gut homing integrin β7 with glaucoma disease severity in patients. Experiments with a glaucoma mouse model showed that β7+ CD4+ T cells need a detour to the gut, where they undergo genetic reprogramming to gain retinal access. Blocking mucosal addressin cell adhesion molecule 1 prevented retinal infiltration of β7+ CD4+ T cells and ameliorated the loss of retinal ganglion cells. These findings highlight the importance of the gut-retina axis for glaucoma disease progression. Daniela Neuhofer

Abstract
Glaucoma is the leading cause of irreversible blindness. Currently, most therapeutic strategies aim to reduce elevated intraocular pressure (EIOP), but this does not always halt disease progression. Evidence suggests a role for T cells in glaucoma pathogenesis, but the underlying mechanisms remain largely unknown. Here, we found that the percentage of circulating CD4+ T cells expressing a gut-homing integrin β7 was increased in patients with glaucoma and was associated with disease stage. In an EIOP-triggered glaucoma mouse model, β7+ CD4+ T cells infiltrated the retina in the progressive phase of glaucoma via eliciting retinal endothelial cell expression of mucosal vascular addressin cell adhesion molecule 1 (MAdCAM-1). MAdCAM-1 was minimally detected in retinas of healthy mice, and neutralization with an MAdCAM-1 antibody ameliorated retinal ganglion cell (RGC) loss and glial activity in mice with glaucoma. We furthermore found that EIOP-induced β7+ CD4+ T cells homed to the gut during the acute phase of glaucoma, which was essential for progressive RGC damage in diseased mice. Gut-homing β7+ CD4+ T cells underwent transcriptional reprogramming, showing up-regulated pathways enriched in autoimmune diseases, bacteria responses, mucosal immunity, and glial activity. Gut-homing β7+ CD4+ T cells gained the competence to induce retinal MAdCAM-1 expression and to cross the blood-retina barrier. Together, our study reveals a role of gut-licensed β7+ CD4+ T cells and MAdCAM-1 in RGC degeneration and emphasizes the importance of the “gut-retina” axis in glaucoma.

Gut-licensed β7+ CD4+ T cells contribute to progressive retinal ganglion cell damage in glaucoma | Science Translational Medicine

 

[Sly Saint]

article about the paper
Weird 'gut-eye axis' links the retina and intestines, and may help explain glaucoma (msn.com)