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Updated: Jan 16, 2026

Experimental Autoimmune Uveitis: An Intraocular Inflammatory Mouse Model
Published on: January 12, 2022
Evaluating the Effectiveness of Escalating to Weekly Adalimumab Dosing for the Treatment of Noninfectious Uveitis: A
Shani Pillar1, Akshay Thomas2, Lynn Hassman3
1Ocular Inflammatory Disease Center, UCLA Jules Stein Eye Institute, University of California, Los Angeles, Los Angeles, California; Department of Ophthalmology, David Geffen School of Medicine at UCLA, University of California, Los Angels, Los Angeles, California.
Purpose:
To evaluate the effectiveness of adalimumab dosage escalation in patients with noninfectious uveitis that is controlled inadequately with standard dosing.
Design:
Multicenter retrospective interventional case series.
Participants:
Patients with noninfectious uveitis receiving active standard biweekly adalimumab dosing who underwent treatment escalation to weekly adalimumab dosing at 6 tertiary referral centers.
Methods:
Demographic data and clinical findings were assessed at the time of adalimumab dosage escalation and 6 months later. Mixed-model analysis was performed to analyze clinical outcomes and to assess predictive factors of success.
Main Outcome Measures:
Treatment success composite criteria included: (1) disease quiescence (≤ 0.5+ anterior chamber cell, ≤ 0.5+ vitreous haze, inactive retinal or choroidal lesions), (2) prednisone 7.5 mg/day or less, and (3) 2 drops/day or less of prednisolone or equivalent (4) no treatment discontinuation.
Results:
Fifty patients (mean ± standard deviation age, 44.4 ± 21.2 years; n = 35 female patients) from 6 tertiary referral centers were included. At 6 months after adalimumab escalation (median, 184 days), 52% of patients had achieved treatment success. Specific inflammatory signs significantly reduced after adalimumab escalation included anterior chamber cell grade (P = 0.025) and presence of active retinal or choroidal lesions (P = 0.010). Prednisone was decreased from more than 7.5 mg/day to lower dosages in 63% of patients (P = 0.015). The odds ratio for treatment success was 6.88 for patients with posterior uveitis (P = 0.024) and 0.14 (P = 0.005) for patients with panuveitis. The hazard ratio for treatment success was 3.73 (P = 0.009) for eyes with active retinal vasculitis at the time of adalimumab escalation.
Conclusions:
Escalation from standard biweekly adalimumab dosing to weekly adalimumab dosing achieved treatment success in more than half of the patients. Posterior uveitis predicts a favorable chance of success, whereas panuveitis conveys a lower success rate.
Financial Disclosure(S):
Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
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