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


Journal

Eye (London, England)
ISSN: 1476-5454
Titre abrégé: Eye (Lond)
Pays: England
ID NLM: 8703986

Informations de publication

Date de publication:
19 Aug 2023
Historique:
received: 01 04 2023
accepted: 10 08 2023
revised: 30 07 2023
medline: 20 8 2023
pubmed: 20 8 2023
entrez: 19 8 2023
Statut: aheadofprint

Résumé

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. 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. 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. 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.

Sections du résumé

BACKGROUND 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 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 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 CONCLUSIONS
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.

Identifiants

pubmed: 37598261
doi: 10.1038/s41433-023-02706-6
pii: 10.1038/s41433-023-02706-6
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Commentaires et corrections

Type : UpdateOf

Informations de copyright

© 2023. The Author(s), under exclusive licence to The Royal College of Ophthalmologists.

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Auteurs

Amr M Zaki (AM)

Casey Eye Institute, Oregon Health & Science University, Portland, OR, USA.

Sirichai Pasadhika (S)

Legacy Devers Eye Institute, Portland, OR, USA.

Jerry C Huang (JC)

Department of Ophthalmology, Keelung Chang Gung Memorial Hospital, Keelung, Taiwan.

Akshay S Thomas (AS)

Tennessee Retina, Nashville, TN, USA.

Bryn M Burkholder (BM)

Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Lyndell L Lim (LL)

Centre for Eye Research Australia, University of Melbourne, Parkville, VIC, Australia.
Royal Victorian Eye and Ear Hospital, Melbourne, VIC, Australia.

Stephanie M Llop (SM)

Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL, USA.

Eric B Suhler (EB)

Casey Eye Institute, Oregon Health & Science University, Portland, OR, USA.
Portland Veterans Administration Health Care System, Portland, OR, USA.

Grazyna Adamus (G)

Casey Eye Institute, Oregon Health & Science University, Portland, OR, USA.

James T Rosenbaum (JT)

Casey Eye Institute, Oregon Health & Science University, Portland, OR, USA. rosenbaumjames04@gmail.com.
Legacy Devers Eye Institute, Portland, OR, USA. rosenbaumjames04@gmail.com.
Department of Medicine, Oregon Health & Science University, Portland, OR, USA. rosenbaumjames04@gmail.com.
Corvus Pharmaceuticals, Burlingame, CA, USA. rosenbaumjames04@gmail.com.

Classifications MeSH