Ocular Vascular Diseases: From Retinal Immune Privilege to Inflammation.

Int J Mol Sci

Department of Ophthalmology, Harvard Medical School, Boston Children's Hospital, Boston, MA 02115, USA.

Published: July 2023

AI Article Synopsis

  • The eye is considered an immune privileged area, meaning it protects its visual functions from immune attacks, but if this privilege is compromised, inflammation can occur.
  • When immune responses are activated, microglia in the retina respond by releasing factors to safeguard retinal cells, but prolonged inflammation can lead to damage and vision problems.
  • The review highlights the characteristics of immune privilege in the retina, the inflammatory processes involved when this privilege fails, and recent advancements in understanding and treating eye diseases such as retinopathy of prematurity, age-related macular degeneration, and diabetic retinopathy.

Article Abstract

The eye is an immune privileged tissue that insulates the visual system from local and systemic immune provocation to preserve homeostatic functions of highly specialized retinal neural cells. If immune privilege is breached, immune stimuli will invade the eye and subsequently trigger acute inflammatory responses. Local resident microglia become active and release numerous immunological factors to protect the integrity of retinal neural cells. Although acute inflammatory responses are necessary to control and eradicate insults to the eye, chronic inflammation can cause retinal tissue damage and cell dysfunction, leading to ocular disease and vision loss. In this review, we summarized features of immune privilege in the retina and the key inflammatory responses, factors, and intracellular pathways activated when retinal immune privilege fails, as well as a highlight of the recent clinical and research advances in ocular immunity and ocular vascular diseases including retinopathy of prematurity, age-related macular degeneration, and diabetic retinopathy.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10418793PMC
http://dx.doi.org/10.3390/ijms241512090DOI Listing

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