Related Experiment Video
Updated: Jan 30, 2026

A Chronic Autoimmune Dry Eye Rat Model with Increase in Effector Memory T Cells in Eyeball Tissue
Published on: June 7, 2017
Immune Cell Infiltration into the Eye Is Controlled by IL-10 in Recoverin-Induced Autoimmune Retinopathy
Enayat Nikoopour1,2,3, Cheng-Mao Lin1, Sarah Sheskey1
1Department of Ophthalmology and Visual Sciences-Kellogg Eye Center, University of Michigan Medical School, Ann Arbor, MI 48105.
Autoimmune retinopathy (AIR) involves vision loss driven by T cell responses to recoverin. This study introduces a new mouse model showing T cells are key drivers, with IL-10 crucial for protection.
Area of Science:
- Ophthalmology
- Immunology
- Autoimmune Diseases
Background:
- Autoimmune retinopathy (AIR) causes progressive vision loss.
- AIR is linked to an immune imbalance involving T helper 1 (TH1) and regulatory T cells targeting the retinal protein recoverin.
Purpose of the Study:
- To establish a novel murine model for studying AIR immunopathology.
- To investigate the role of T cell responses to recoverin in AIR pathogenesis.
Main Methods:
- Immunization of C57BL/6 mice with recoverin.
- Utilizing IL-10 knockout (KO) mice to assess disease kinetics and severity.
- Employing an immunodominant recoverin peptide (AG-16) and adoptive cell transfer.
Main Results:
- Recoverin immunization induced ocular inflammation with immune cell infiltration.
- IL-10 KO mice showed exacerbated inflammation and accelerated disease.
- Adoptive transfer of recoverin-specific T cells induced AIR, while B cell deficiency resulted in milder disease.
Conclusions:
- T cell responses to recoverin are critical drivers of AIR.
- IL-10 plays a significant protective role in preventing AIR development.
Related Concept Videos
What is the Immune System?
Autoimmune Disorders
Concept and Mechanism of Autoimmune Diseases
The immune...
The Cell Cycle Control System
Cyclins and cyclin-dependent kinases (Cdks) are the primary cell cycle regulators and...
The Cell Cycle Control System
Cell-mediated Immune Responses
Cells of the Adaptive Immune Response

