Sulejmani Nimisha, Nagai Shunji, Safwan Mohamed, Rizzari Michael D, Raoufi Mohammad, Abouljoud Marwan S, Ramesh Mayur
Department of Pharmacy, Henry Ford Hospital, Detroit, Michigan.
Division of Transplant and Hepatobiliary Surgery, Henry Ford Hospital, Detroit, Michigan.
Pharmacotherapy. 2018 Apr;38(4):470-475. doi: 10.1002/phar.2094. Epub 2018 Mar 28.
Adenoviruses are double-stranded DNA viruses that typically cause mild self-limiting respiratory, ocular, and gastrointestinal infections. In immunocompromised patients, especially transplant recipients, the infection can be severe, with dissemination and multiorgan failure. In intestinal transplant recipients, the incidence is as high as 57%. To our knowledge, no standardized guidelines or U.S. Food and Drug Administration-approved medications exist for the treatment of adenovirus disease.
We describe two isolated intestinal transplant recipients who developed adenovirus disease (viremia with viral enteritis) that was managed with a new experimental drug, brincidofovir (an oral lipid conjugate prodrug of cidofovir), as salvage therapy.
The first patient was a 44-year-old woman who developed adenoviral enteritis 1 month after transplantation, which resolved with ribavirin therapy. Two weeks later, the infection recurred, and brincidofovir was initiated. While receiving this therapy for 3 months, she developed severe acute rejection, which was managed with rabbit antithymocyte globulin followed by infliximab. Eventually, complete resolution of the rejection and adenoviral enteritis was achieved. At 12 months posttransplantation, the patient was healthy and tolerating enteral feeding. The second patient was a 28-year-old man who had undergone isolated intestinal transplantation 6 years before he presented with generalized weakness and an increased ostomy output; he was diagnosed with adenoviral enteritis. Maintenance immunosuppression was reduced, and brincidofovir was started. The infection resolved with a month of therapy. Six months after the infection, he was healthy and tolerating enteral feeding.
This is the first publication, to our knowledge, to describe two cases in which brincidofovir was used to successfully treat adenovirus infection in intestinal transplant recipients. Thus, these cases demonstrate that brincidofovir appears to be a safe and effective option in the management of adenoviral enteritis in these patients.
腺病毒是双链DNA病毒,通常引起轻度自限性呼吸道、眼部和胃肠道感染。在免疫功能低下的患者中,尤其是移植受者,感染可能很严重,会出现播散和多器官功能衰竭。在肠道移植受者中,发病率高达57%。据我们所知,目前尚无治疗腺病毒疾病的标准化指南或美国食品药品监督管理局批准的药物。
我们描述了两名孤立的肠道移植受者,他们患上了腺病毒疾病(病毒血症伴病毒性肠炎),使用一种新的实验性药物布林西多福韦(西多福韦的口服脂质共轭前药)作为挽救疗法进行治疗。
第一名患者是一名44岁女性,移植后1个月发生腺病毒性肠炎,接受利巴韦林治疗后痊愈。两周后,感染复发,开始使用布林西多福韦。在接受该治疗3个月时,她发生了严重的急性排斥反应,用兔抗胸腺细胞球蛋白治疗,随后使用英夫利昔单抗。最终,排斥反应和腺病毒性肠炎完全缓解。移植后12个月,患者健康,能够耐受肠内喂养。第二名患者是一名28岁男性,在出现全身无力和造口排出量增加前6年接受了孤立性肠道移植;他被诊断为腺病毒性肠炎。维持性免疫抑制治疗减少,开始使用布林西多福韦。经过1个月的治疗,感染得到缓解。感染6个月后,他健康,能够耐受肠内喂养。
据我们所知,这是首次发表的描述两例使用布林西多福韦成功治疗肠道移植受者腺病毒感染的病例。因此,这些病例表明,布林西多福韦似乎是治疗这些患者腺病毒性肠炎的一种安全有效的选择。