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Anti-retinal Autoantibodies in Hydroxychloroquine Eye Toxicity
Samuel D Good1, Grazyna Adamus2, Michael B Gorin3
1David Geffen School of Medicine, Division of Rheumatology, University of California Los Angeles, Los Angeles, USA.
ACR Open Rheumatology
|November 8, 2024
Summary
Patients with hydroxychloroquine (HCQ) retinopathy showed higher levels of anti-retinal autoantibodies (AAbs), particularly anti-arrestin AAbs. These autoantibodies may serve as a biomarker for HCQ-related eye toxicity in patients with systemic lupus erythematosus.
Area of Science:
- Ophthalmology
- Rheumatology
- Immunology
Background:
- Autoimmune retinopathy and hydroxychloroquine (HCQ)-related retinal toxicity share clinical similarities.
- This suggests a potential role for autoimmunity in HCQ retinopathy.
Purpose of the Study:
- To investigate the association between circulating antiretinal autoantibodies (AAbs) and HCQ retinal toxicity.
- To determine if patients with HCQ retinal toxicity are more likely to have AAbs compared to controls.
Main Methods:
- Plasma samples from 270 patients with systemic lupus erythematosus (SLE) on HCQ were tested for anti-retinal AAbs using immunoblotting.
- Patients were assessed for HCQ retinal toxicity and other risk factors via chart review.
- Multivariate logistic regression was used to compare AAb frequencies between patients with and without retinal toxicity.
Main Results:
- Patients with HCQ retinal toxicity had significantly higher rates of anti-arrestin AAbs (60.7% vs 30.6%) and anti-pyruvate kinase M2 AAbs (46.4% vs 28.1%).
- A higher mean number of total anti-retinal AAbs was observed in patients with HCQ eye toxicity (3.0 vs 2.04).
- The presence of anti-arrestin antibodies was linked to a 3.2-fold increased odds of developing HCQ eye toxicity, even after accounting for other risk factors.
Conclusions:
- Anti-retinal AAbs are more prevalent in SLE patients experiencing HCQ retinal toxicity.
- Anti-arrestin AAbs are associated with an increased risk of HCQ eye toxicity.
- Anti-retinal AAbs may serve as a valuable biomarker for identifying HCQ eye toxicity.

