Neutralizing tumor necrosis factor activity leads to remission in patients with refractory noninfectious posterior uveitis.

OBJECTIVE: To evaluate the efficacy and safety of tumor necrosis factor (TNF) inhibition with the p55 TNF receptor fusion protein (TNFr-Ig) for severe sight-threatening noninfectious posterior segment intraocular inflammation. METHODS: Seventeen patients with refractory noninfectious posterior segm...

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Main Authors: Murphy, C, Greiner, K, Plskova, J, Duncan, L, Frost, A, Isaacs, J, Rebello, P, Waldmann, H, Hale, G, Forrester, J, Dick, A
格式: Journal article
语言:English
出版: 2004
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author Murphy, C
Greiner, K
Plskova, J
Duncan, L
Frost, A
Isaacs, J
Rebello, P
Waldmann, H
Hale, G
Forrester, J
Dick, A
author_facet Murphy, C
Greiner, K
Plskova, J
Duncan, L
Frost, A
Isaacs, J
Rebello, P
Waldmann, H
Hale, G
Forrester, J
Dick, A
author_sort Murphy, C
collection OXFORD
description OBJECTIVE: To evaluate the efficacy and safety of tumor necrosis factor (TNF) inhibition with the p55 TNF receptor fusion protein (TNFr-Ig) for severe sight-threatening noninfectious posterior segment intraocular inflammation. METHODS: Seventeen patients with refractory noninfectious posterior segment intraocular inflammation received TNFr-Ig by intravenous infusion in this nonrandomized, open-label, pilot study. The primary outcome measure was logMAR visual acuity. Secondary outcome measures were binocular indirect ophthalmoscopy score, cystoid macular edema, adverse effects, and vision-related (visual core module 1) and health-related (36-Item Short-Form Health Survey) quality of life. RESULTS: Within 1 month of TNFr-Ig therapy, 9 patients (53%) achieved at least a 2-line improvement in visual acuity, 8 (57%) of 14 patients with vitreous haze before treatment achieved an improvement in binocular indirect ophthalmoscopy score to 0, and macular edema resolved in 5 (56%) of 9 affected patients. Twelve (71%) of the patients achieved complete cessation of intraocular inflammation following TNFr-Ig therapy. A reduction in concomitant immunosuppression was possible for 11 patients (65%) following TNFr-Ig therapy. However, all but 1 patient required continuing adjuvant therapy during the response to TNFr-Ig, which had a median duration of 3 months. Adverse effects included mild infusion reactions in 3 patients and transient lymphocytopenia in 2 patients. CONCLUSION: Therapy with TNFr-Ig was safe and effective for treating patients with sight-threatening noninfectious posterior segment intraocular inflammation resistant to conventional immunotherapy, but adjuvant immunosuppression and repeat infusions would be required to maintain long-term remission.
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spelling oxford-uuid:e57dbdf1-0328-4478-901b-57b3cc7fd44e2022-03-27T10:24:22ZNeutralizing tumor necrosis factor activity leads to remission in patients with refractory noninfectious posterior uveitis.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:e57dbdf1-0328-4478-901b-57b3cc7fd44eEnglishSymplectic Elements at Oxford2004Murphy, CGreiner, KPlskova, JDuncan, LFrost, AIsaacs, JRebello, PWaldmann, HHale, GForrester, JDick, A OBJECTIVE: To evaluate the efficacy and safety of tumor necrosis factor (TNF) inhibition with the p55 TNF receptor fusion protein (TNFr-Ig) for severe sight-threatening noninfectious posterior segment intraocular inflammation. METHODS: Seventeen patients with refractory noninfectious posterior segment intraocular inflammation received TNFr-Ig by intravenous infusion in this nonrandomized, open-label, pilot study. The primary outcome measure was logMAR visual acuity. Secondary outcome measures were binocular indirect ophthalmoscopy score, cystoid macular edema, adverse effects, and vision-related (visual core module 1) and health-related (36-Item Short-Form Health Survey) quality of life. RESULTS: Within 1 month of TNFr-Ig therapy, 9 patients (53%) achieved at least a 2-line improvement in visual acuity, 8 (57%) of 14 patients with vitreous haze before treatment achieved an improvement in binocular indirect ophthalmoscopy score to 0, and macular edema resolved in 5 (56%) of 9 affected patients. Twelve (71%) of the patients achieved complete cessation of intraocular inflammation following TNFr-Ig therapy. A reduction in concomitant immunosuppression was possible for 11 patients (65%) following TNFr-Ig therapy. However, all but 1 patient required continuing adjuvant therapy during the response to TNFr-Ig, which had a median duration of 3 months. Adverse effects included mild infusion reactions in 3 patients and transient lymphocytopenia in 2 patients. CONCLUSION: Therapy with TNFr-Ig was safe and effective for treating patients with sight-threatening noninfectious posterior segment intraocular inflammation resistant to conventional immunotherapy, but adjuvant immunosuppression and repeat infusions would be required to maintain long-term remission.
spellingShingle Murphy, C
Greiner, K
Plskova, J
Duncan, L
Frost, A
Isaacs, J
Rebello, P
Waldmann, H
Hale, G
Forrester, J
Dick, A
Neutralizing tumor necrosis factor activity leads to remission in patients with refractory noninfectious posterior uveitis.
title Neutralizing tumor necrosis factor activity leads to remission in patients with refractory noninfectious posterior uveitis.
title_full Neutralizing tumor necrosis factor activity leads to remission in patients with refractory noninfectious posterior uveitis.
title_fullStr Neutralizing tumor necrosis factor activity leads to remission in patients with refractory noninfectious posterior uveitis.
title_full_unstemmed Neutralizing tumor necrosis factor activity leads to remission in patients with refractory noninfectious posterior uveitis.
title_short Neutralizing tumor necrosis factor activity leads to remission in patients with refractory noninfectious posterior uveitis.
title_sort neutralizing tumor necrosis factor activity leads to remission in patients with refractory noninfectious posterior uveitis
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