Role of topical and systemic immunosuppression in aqueous-deficient dry eye disease

Immunosuppression in aqueous-deficient dry eye disease (ADDE) is required not only to improve the symptoms and signs but also to prevent further progression of the disease and its sight-threatening sequelae. This immunomodulation can be achieved through topical and/or systemic medications, and the c...

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Main Authors: Anahita Kate, Swapna S Shanbhag, Pragnya R Donthineni, Guillermo Amescua, Victor L Perez Quinones, Sayan Basu
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2023-01-01
Series:Indian Journal of Ophthalmology
Subjects:
Online Access:http://www.ijo.in/article.asp?issn=0301-4738;year=2023;volume=71;issue=4;spage=1176;epage=1189;aulast=Kate
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author Anahita Kate
Swapna S Shanbhag
Pragnya R Donthineni
Guillermo Amescua
Victor L Perez Quinones
Sayan Basu
author_facet Anahita Kate
Swapna S Shanbhag
Pragnya R Donthineni
Guillermo Amescua
Victor L Perez Quinones
Sayan Basu
author_sort Anahita Kate
collection DOAJ
description Immunosuppression in aqueous-deficient dry eye disease (ADDE) is required not only to improve the symptoms and signs but also to prevent further progression of the disease and its sight-threatening sequelae. This immunomodulation can be achieved through topical and/or systemic medications, and the choice of one drug over the other is determined by the underlying systemic disease. These immunosuppressive agents require a minimum of 6–8 weeks to achieve their beneficial effect, and during this time, the patient is usually placed on topical corticosteroids. Antimetabolites such as methotrexate, azathioprine, and mycophenolate mofetil, along with calcineurin inhibitors, are commonly used as first-line medications. The latter have a pivotal role in immunomodulation since T cells contribute significantly to the pathogenesis of ocular surface inflammation in dry eye disease. Alkylating agents are largely limited to controlling acute exacerbations with pulse doses of cyclophosphamide. Biologic agents, such as rituximab, are particularly useful in patients with refractory disease. Each group of drugs has its own side-effect profiles and requires a stringent monitoring schedule that must be followed to prevent systemic morbidity. A customized combination of topical and systemic medications is usually required to achieve adequate control, and this review aims to help the clinician choose the most appropriate modality and monitoring regimen for a given case of ADDE.
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spelling doaj.art-1cd12edb3bca4c2b910959bfc70323562023-05-18T05:50:41ZengWolters Kluwer Medknow PublicationsIndian Journal of Ophthalmology0301-47381998-36892023-01-017141176118910.4103/IJO.IJO_2818_22Role of topical and systemic immunosuppression in aqueous-deficient dry eye diseaseAnahita KateSwapna S ShanbhagPragnya R DonthineniGuillermo AmescuaVictor L Perez QuinonesSayan BasuImmunosuppression in aqueous-deficient dry eye disease (ADDE) is required not only to improve the symptoms and signs but also to prevent further progression of the disease and its sight-threatening sequelae. This immunomodulation can be achieved through topical and/or systemic medications, and the choice of one drug over the other is determined by the underlying systemic disease. These immunosuppressive agents require a minimum of 6–8 weeks to achieve their beneficial effect, and during this time, the patient is usually placed on topical corticosteroids. Antimetabolites such as methotrexate, azathioprine, and mycophenolate mofetil, along with calcineurin inhibitors, are commonly used as first-line medications. The latter have a pivotal role in immunomodulation since T cells contribute significantly to the pathogenesis of ocular surface inflammation in dry eye disease. Alkylating agents are largely limited to controlling acute exacerbations with pulse doses of cyclophosphamide. Biologic agents, such as rituximab, are particularly useful in patients with refractory disease. Each group of drugs has its own side-effect profiles and requires a stringent monitoring schedule that must be followed to prevent systemic morbidity. A customized combination of topical and systemic medications is usually required to achieve adequate control, and this review aims to help the clinician choose the most appropriate modality and monitoring regimen for a given case of ADDE.http://www.ijo.in/article.asp?issn=0301-4738;year=2023;volume=71;issue=4;spage=1176;epage=1189;aulast=Katecalcineurin inhibitorscorticosteroidsdry eye diseaseimmunosuppressive agentsmucous membrane pemphigoidsjogren's syndromesteroid-sparing agents
spellingShingle Anahita Kate
Swapna S Shanbhag
Pragnya R Donthineni
Guillermo Amescua
Victor L Perez Quinones
Sayan Basu
Role of topical and systemic immunosuppression in aqueous-deficient dry eye disease
Indian Journal of Ophthalmology
calcineurin inhibitors
corticosteroids
dry eye disease
immunosuppressive agents
mucous membrane pemphigoid
sjogren's syndrome
steroid-sparing agents
title Role of topical and systemic immunosuppression in aqueous-deficient dry eye disease
title_full Role of topical and systemic immunosuppression in aqueous-deficient dry eye disease
title_fullStr Role of topical and systemic immunosuppression in aqueous-deficient dry eye disease
title_full_unstemmed Role of topical and systemic immunosuppression in aqueous-deficient dry eye disease
title_short Role of topical and systemic immunosuppression in aqueous-deficient dry eye disease
title_sort role of topical and systemic immunosuppression in aqueous deficient dry eye disease
topic calcineurin inhibitors
corticosteroids
dry eye disease
immunosuppressive agents
mucous membrane pemphigoid
sjogren's syndrome
steroid-sparing agents
url http://www.ijo.in/article.asp?issn=0301-4738;year=2023;volume=71;issue=4;spage=1176;epage=1189;aulast=Kate
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AT pragnyardonthineni roleoftopicalandsystemicimmunosuppressioninaqueousdeficientdryeyedisease
AT guillermoamescua roleoftopicalandsystemicimmunosuppressioninaqueousdeficientdryeyedisease
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