- Letter to the Editor
- Open Access
Refractory necrotizing scleritis successfully treated with adalimumab
© The Author(s). 2016
- Received: 12 April 2016
- Accepted: 29 September 2016
- Published: 12 October 2016
Necrotizing scleritis is the most severe and destructive form of scleritis with vision-threatening sequelae. It is divided into with inflammation and without inflammation (scleromalacia perforans). Adalimumab is a tumour necrosis factor (TNF)-inhibiting anti-inflammatory medication licensed for the treatment of rheumatoid and psoriatic arthritis, ankylosing spondylitis and inflammatory bowel disease (in the USA). We report two cases of necrotizing scleritis successfully treated with adalimumab.
- Necrotizing scleritis
- TNF inhibitors
A 40-year-old lady presented with a history of scleritis for which she was on oral prednisolone for over 1 year with doses ranging from 10 to 80 mg per day. She had pain and discomfort. Her visual acuity was 6/6 and posterior segment was normal. Examination revealed an area of scleral necrosis.
As her scleritis was active, she was commenced on prednisolone 80 mg and mycophenolate mofetil (MMF) (Cellcept) 500 mg BD, increasing to 750 mg BD. However, she had severe gastric discomfort and nausea and was unable to continue with MMF. She was subsequently put on tacrolimus (Prograf) 7.5 mg but developed nausea and lethargy on this. She was unable to reduce oral steroids whilst oral immunosuppression was tried. She was then started on adalimumab (Humira) subcutaneous 40 mg fortnightly and methotrexate 12.5 mg OD and achieved resolution and control of scleral necrosis after 4 weeks. During the course of treatment, she developed one episode of gastroenteritis during which she missed her Humira. At 9-month follow-up, the disease has remained quiet on two weekly subcutaneous adalimumab treatments.
Side effects during treatment included one episode of shingles.
Necrotizing scleritis represents 10–15 % of cases of anterior scleritis and is the most severe . Left untreated, necrotizing scleritis has a rapid and destructive course that can be sight threatening.
Conventional treatment for recurrent or severe cases of necrotizing scleritis involves immunosuppression therapy and high-dose oral steroids . Side effects associated with these treatments and a poor response may require patients to terminate treatment (as did our two patients), making this condition very difficult to manage.
The predominant cytokine TNF-alpha induces the matrix metalloproteinases (MMPs) enzymes, MMP-3 and MMP-9 . These are predominantly responsible for the destruction of the scleral wall and adjacent cornea in severe scleritis, particularly associated with necrosis .
Infliximab (Remicade Centocor, Johnson & Johnson, USA) and adalimumab (Humira, Abbott Laboratories, Chicago, IL) are monoclonal antibodies that recognise, bind to and inhibit TNF, thereby decreasing inflammation.
Infliximab has shown long-term efficacy in the treatment of refractory posterior uveitis . Published literature has reported improvement in patients with either idiopathic scleritis or scleritis associated with systemic disease treated with infliximab .
Ragam et al. evaluated the use of TNF inhibitors infliximab and adalimumab in 17 patients with non-infectious and non-necrotizing scleritis and achieved control of active inflammation for at least 2 months in 15 (88 %) of 17 patients .
Morarji et al. reported the successful treatment of necrotizing scleritis (secondary to granulomatosis with polyangiitis) with infliximab whilst waiting for rituximab to induce disease remission . Two intravenous 1-g doses of rituximab (MabThera, Hoffmann-La Roche, Ltd.) (a chimeric murine and human monoclonal antibody directed against the CD20 antigen ) were used, given 2 weeks apart. However after 3 weeks, the necrotizing scleritis was still active. Therefore, infusions of infliximab (Remicade, Merck & Co.) 5 mg/kg doses at baseline, 2, 6 and 12 weeks were given, controlling the necrotizing scleritis by week 6. This enabled cyclophosphamide to be avoided in the acute phase (as rituximab can take up to 6 months to work).
In this case series, we report two cases of refractory necrotizing scleritis that were successfully treated with adalimumab. During treatment, one patient developed gastroenteritis and the other developed shingles.
Known potential side effects have been documented in clinical trials and postmarket surveillance with TNF inhibitor use. The development of injection site reactions , infusion reactions , and the reactivation of latent tuberculosis  is increased with TNF inhibitor use. Therefore, proper screening of patients with the tuberculin skin test and chest x-ray and/or interferon gamma assay should be performed prior to initiating these therapies. Other side effects include the development of demyelinating disease  and heart failure .
In conclusion, despite the risks involved with TNF inhibitor use, with adequate screening of patients, the present case series highlights that adalimumab offers a new tool for the treatment of refractory necrotizing scleritis when conventional treatments are contraindicated or have failed.
We thank the photography department at Moorfields Eye Hospital Dubai for help in preparation of the images. All persons who have made substantial contributions to the work reported in the manuscript (e.g., technical help, writing and editing assistance, general support), but who do not meet the criteria for authorship, are named in the Acknowledgements and have given us their written permission to be named.
All persons who meet authorship criteria are listed as authors, and all authors certify that they have participated sufficiently in the work to take public responsibility of this manuscript. Furthermore, each author certifies that this material or similar material has not been and will not be submitted to or published in any other publication before its appearance in the Journal of Ophthalmic Inflammation and Infection. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
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