TY - JOUR
T1 - New observations and emerging ideas in diagnosis and management of non-infectious uveitis
T2 - A review
AU - Rosenbaum, James T.
AU - Bodaghi, Bahram
AU - Couto, Cristobal
AU - Zierhut, Manfred
AU - Acharya, Nisha
AU - Pavesio, Carlos
AU - Tay-Kearney, Mei Ling
AU - Neri, Piergiorgio
AU - Douglas, Kevin
AU - Pathai, Sophia
AU - Song, Alexandra P.
AU - Kron, Martina
AU - Foster, C. Stephen
N1 - Funding Information:
Funding source: This review was sponsored by AbbVie Inc. (North Chicago, IL). The sponsor participated in the manuscript preparation, review, and approval.
Funding Information:
Funding source: This review was sponsored by AbbVie Inc. (North Chicago, IL). The sponsor participated in the manuscript preparation, review, and approval. Declaration of interest: CSF has served as a consultant for Aldeyra, Bausch & Lomb Surgical, EyeGate, Novartis, pSivida, and Xoma; has served as a paid speaker for Alcon and Allergan; and has received grants or has grants pending from Alcon, Aldeyra, Bausch & Lomb, Clearside Biomedical, Dompe, Icon, Novartis, Santen, Xoma, Aciont, and pSivida. JTR was a consultant for AbbVie, Gilead, Regeneron, UCB, Novartis, Topivert, Janssen, Roche, Santen, and Eyevensys; has received financial support from Pfizer; owns stock in Novartis and has received royalties from UpToDate. BB has served on the advisory boards of AbbVie, Allergan, and Santen and has received financial support from Novartis, Bayer, and Roche. CC has nothing to disclose. MZ has served on scientific advisory boards for AbbVie and Santen. NA has served as a consultant for AbbVie and Santen. CP has received a research grant from Alcon; has served as a consultant for Xoma, Servier, and Santen; and has served on the advisory board for Xoma, Servier, Santen, Alcon, and Bausch & Lomb. MLTK was an investigator in the HURON clinical trial for AbbVie and has received speaking fees from AbbVie. PN has served as a consultant for AbbVie, Santen, and Allergan. KD and APS are employees of AbbVie Inc. SP is an employee of AbbVie Ltd. UK. MKron is an employee of AbbVie Deutschland GmbH & Co KG.
Publisher Copyright:
© 2019 The Authors
PY - 2019/12
Y1 - 2019/12
N2 - Background: Non-infectious uveitis (NIU) is an immune-mediated disease with clinical symptoms such as eye pain, redness, floaters, and light sensitivity. NIU is one of the leading causes of preventable blindness. Objective: This review describes current and emerging therapies for NIU. Methods: PubMed searches were conducted using the terms uveitis, therapy, corticosteroids, immunomodulators, biologics, intravitreal injections, intraocular implants, and adverse events deemed relevant if they presented data relating to prevalence, diagnosis, and treatment of uveitis. Results: Diagnosis and management of NIU may require collaboration among different healthcare providers, including ophthalmologists and rheumatologists. Although many patients with NIU respond to corticosteroid (CS) therapy, long-term CS use can be associated with potentially severe adverse events. Localized CS therapies have been developed to reduce adverse events; however, some intravitreal injections and intraocular implants were linked to elevated intraocular pressure and cataracts. CS-sparing therapies such as biologics have demonstrated efficacy and safety while reducing CS burden. Biologics targeting tumor necrosis factor provide CS-sparing options for patients with NIU. Additional studies are needed to address long-term efficacy and safety of biologics targeting IL-6 and inhibitors of JAK/STAT. Conclusion: Biologics, JAK/STAT inhibitors, and improved localized therapies may provide additional options for patients with NIU.
AB - Background: Non-infectious uveitis (NIU) is an immune-mediated disease with clinical symptoms such as eye pain, redness, floaters, and light sensitivity. NIU is one of the leading causes of preventable blindness. Objective: This review describes current and emerging therapies for NIU. Methods: PubMed searches were conducted using the terms uveitis, therapy, corticosteroids, immunomodulators, biologics, intravitreal injections, intraocular implants, and adverse events deemed relevant if they presented data relating to prevalence, diagnosis, and treatment of uveitis. Results: Diagnosis and management of NIU may require collaboration among different healthcare providers, including ophthalmologists and rheumatologists. Although many patients with NIU respond to corticosteroid (CS) therapy, long-term CS use can be associated with potentially severe adverse events. Localized CS therapies have been developed to reduce adverse events; however, some intravitreal injections and intraocular implants were linked to elevated intraocular pressure and cataracts. CS-sparing therapies such as biologics have demonstrated efficacy and safety while reducing CS burden. Biologics targeting tumor necrosis factor provide CS-sparing options for patients with NIU. Additional studies are needed to address long-term efficacy and safety of biologics targeting IL-6 and inhibitors of JAK/STAT. Conclusion: Biologics, JAK/STAT inhibitors, and improved localized therapies may provide additional options for patients with NIU.
KW - Adalimumab
KW - Biologics
KW - Corticosteroid-sparing therapy
KW - Immune-mediated disease
KW - Noninfectious uveitis
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UR - http://www.scopus.com/inward/citedby.url?scp=85068583951&partnerID=8YFLogxK
U2 - 10.1016/j.semarthrit.2019.06.004
DO - 10.1016/j.semarthrit.2019.06.004
M3 - Review article
C2 - 31301816
AN - SCOPUS:85068583951
SN - 0049-0172
VL - 49
SP - 438
EP - 445
JO - Seminars in Arthritis and Rheumatism
JF - Seminars in Arthritis and Rheumatism
IS - 3
ER -