Literature DB >> 27442322

Ocular Manifestations of Inherited Phospholipase-Cγ2-Associated Antibody Deficiency and Immune Dysregulation.

Antonio Di Zazzo1, Maryam Tahvildari, George J Florakis, Reza Dana.   

Abstract

PURPOSE: To report the ocular manifestations of phospholipase-Cγ2-associated antibody deficiency and immune dysregulation (PLAID).
METHODS: Case report and literature review.
RESULTS: A 21-year-old woman diagnosed with PLAID was referred for evaluation of repeated episodes of ocular inflammation resulting in bilateral peripheral corneal pannus with episcleritis and corneal scarring accompanied by systemic manifestations including epidermolysis bullosa and interstitial lung disease. Systemic immunosuppression with corticosteroids and interleukin-1 (IL-1) receptor antagonist (anakinra) was supplemented with topical anakinra to avoid systemic side effects, which resulted in partial improvement of the ocular symptoms. Oral prednisone was restarted to treat active lesions during bouts of inflammation.
CONCLUSIONS: Ocular PLAID is a bilateral chronic or recurrent inflammatory disease of the ocular surface leading to severe and early cicatricial ocular surface and corneal involvement because of high IL-1 production. Management of PLAID may require both topical and systemic immunomodulatory treatments, potentially including targeted local anti-IL-1 therapy.

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Year:  2016        PMID: 27442322      PMCID: PMC5250612          DOI: 10.1097/ICO.0000000000000951

Source DB:  PubMed          Journal:  Cornea        ISSN: 0277-3740            Impact factor:   2.651


  8 in total

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2.  Cytokine expression in the alkali-burned cornea.

Authors:  C Sotozono; J He; Y Matsumoto; M Kita; J Imanishi; S Kinoshita
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4.  Prevention of allergic eye disease by treatment with IL-1 receptor antagonist.

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5.  Cold urticaria, immunodeficiency, and autoimmunity related to PLCG2 deletions.

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6.  Topical interleukin 1 receptor antagonist for treatment of dry eye disease: a randomized clinical trial.

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7.  A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiency.

Authors:  Qing Zhou; Geun-Shik Lee; Jillian Brady; Shrimati Datta; Matilda Katan; Afzal Sheikh; Marta S Martins; Tom D Bunney; Brian H Santich; Susan Moir; Douglas B Kuhns; Debra A Long Priel; Amanda Ombrello; Deborah Stone; Michael J Ombrello; Javed Khan; Joshua D Milner; Daniel L Kastner; Ivona Aksentijevich
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8.  Cutting Edge: IL-1 Receptor Signaling is Critical for the Development of Autoimmune Uveitis.

Authors:  Chi-Keung Wan; Chang He; Lin Sun; Charles E Egwuagu; Warren J Leonard
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  8 in total
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1.  Severe Autoinflammatory Manifestations and Antibody Deficiency Due to Novel Hypermorphic PLCG2 Mutations.

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  1 in total

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