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. 2024 Feb;38(2):386-392.
doi: 10.1038/s41433-023-02706-6. Epub 2023 Aug 19.

Characterization of autoimmune eye disease in association with Down's syndrome

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Characterization of autoimmune eye disease in association with Down's syndrome

Amr M Zaki et al. Eye (Lond). 2024 Feb.

Abstract

Background: Autoimmunity and deficiency of the transcription factor autoimmune regulator protein (AIRE) are known associations with Down syndrome (DS). Lack of AIRE abrogates thymic tolerance. The autoimmune eye disease associated with DS has not been characterized. We identified a series of subjects with DS (n = 8) and uveitis. In three consecutive subjects, we tested the hypothesis that autoimmunity to retinal antigens might be a contributing factor.

Subjects/methods: This was a multicentred, retrospective case series. Deidentified clinical data of subjects with both DS and uveitis were collected via questionnaire by uveitis-trained ophthalmologists. Anti-retinal autoantibodies (AAbs) were detected using an Autoimmune Retinopathy Panel tested in the OHSU Ocular Immunology Laboratory.

Results: We characterized eight subjects (mean age 29 [range, 19-37] years). The mean age of detected uveitis onset was 23.5 [range, 11-33] years. All eight subjects had bilateral uveitis (p < 0.001 based on comparison to published university referral patterns), with anterior and intermediate uveitis found in six and five subjects respectively. Each of three subjects tested for anti-retinal AAbs was positive. Detected AAbs included anti-carbonic anhydrase II, anti-enolase, anti-arrestin, and anti-aldolase.

Discussion: A partial deficiency in the AIRE on chromosome 21 has been described in DS. The similarities in the uveitis presentations within this patient group, the known autoimmune disease predisposition in DS, the recognized association of DS and AIRE deficiency, the reported detection of anti-retinal antibodies in patients with DS in general, and the presence of anti-retinal AAbs in three subjects in our series supports a causal association between DS and autoimmune eye disease.

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Conflict of interest statement

AST: consultant for Alimera, Allergan, Avesis, Bausch & Lomb, Eyepoint, Genentech, Zeiss. SML: Eyepoint Pharmaceuticals. JTR: consultant for Abbvie, Gilead, Roche, Horizon, Eyevensys, Santen, UCB, Corvus, and Affibody; royalties from UpToDate; clinical trial support from Pfizer and Horizon; and data monitoring for BMS-Celgene and Lilly. The remaining authors declare no competing interests.

Figures

Fig. 1
Fig. 1. Representative ophthalmic imaging.
a Optos fundus fluorescein angiography of subject 7 showing bilateral optic disc hyperfluorescence and diffuse vascular leakage. b Spectral domain-optical coherence tomography (SD-OCT) of subject 8 showing bilateral ellipsoid zone disruption (white arrows).

Update of

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