Iwahashi Chiharu, Ono Hikari, Haruta Mami, Minami Takamasa, Mashimo Hisashi, Shimojo Hiroshi, Ohguro Nobuyuki
Ophthalmology, Sumitomo Hospital, Osaka, Japan.
Ophthalmology, Kindai University Faculty of Medicine Hospital, Osakasayama, Japan.
BMJ Open Ophthalmol. 2019 Jul 7;4(1):e000250. doi: 10.1136/bmjophth-2018-000250. eCollection 2019.
To report four cases of new onset or exacerbation of uveitis following administration of infliximab.
This retrospective observational case series includes four patients who developed new onset or exacerbation of uveitis paradoxically during infliximab treatment.
Four patients were assessed, including three women, with a mean age of 33 (14-84) years. Infliximab was introduced for the treatment of scleritis associated with rheumatoid arthritis (two cases), chronic anterior uveitis associated with juvenile idiopathic arthritis (JIA) (one case) and Crohn's disease (one case). Anterior scleritis associated with rheumatoid arthritis successfully improved following infliximab administration; however, macular oedema or dense vitritis paradoxically developed in two cases. In one case, infliximab was switched to tocilizumab. In another case, infliximab was discontinued, and additional corticosteroids and immunosuppressive medications were added. In one patient with JIA, new-onset macular oedema and exacerbation of anterior uveitis were observed during infliximab treatment, so the patient was switched to adalimumab. In the patient with Crohn's disease treated with infliximab, severe vasculitis and macular oedema occurred, requiring intravitreal triamcinolone injection. The patient was switched to adalimumab. Given that these reactions were paradoxical effects of infliximab, infliximab treatment was discontinued in all cases, and additional corticosteroids or immunosuppressive medications were added. All cases remained free of ocular inflammation at the last visit.
Uveitis rarely occurs de novo or is exacerbated during infliximab treatment. Cessation of infliximab led to resolution of this paradoxical adverse effect.
报告4例使用英夫利昔单抗后新发葡萄膜炎或葡萄膜炎加重的病例。
本回顾性观察病例系列包括4例在英夫利昔单抗治疗期间反常地出现新发葡萄膜炎或葡萄膜炎加重的患者。
评估了4例患者,其中包括3名女性,平均年龄为33(14 - 84)岁。英夫利昔单抗用于治疗与类风湿关节炎相关的巩膜炎(2例)、与幼年特发性关节炎(JIA)相关的慢性前葡萄膜炎(1例)和克罗恩病(1例)。英夫利昔单抗治疗后,与类风湿关节炎相关的前巩膜炎成功改善;然而,2例患者反常地出现黄斑水肿或严重玻璃体炎。1例患者将英夫利昔单抗换为托珠单抗。另1例患者停用英夫利昔单抗,并加用了其他皮质类固醇和免疫抑制药物。1例JIA患者在英夫利昔单抗治疗期间出现新发黄斑水肿和前葡萄膜炎加重,因此将该患者换为阿达木单抗。在用英夫利昔单抗治疗的克罗恩病患者中,发生了严重血管炎和黄斑水肿,需要玻璃体内注射曲安奈德。该患者换为阿达木单抗。鉴于这些反应是英夫利昔单抗的反常效应,所有病例均停用英夫利昔单抗,并加用了其他皮质类固醇或免疫抑制药物。在最后一次随访时,所有病例均无眼部炎症。
葡萄膜炎很少在英夫利昔单抗治疗期间新发或加重。停用英夫利昔单抗可使这种反常的不良反应得到缓解。