Terrec Florian, Jouve Thomas, Malvezzi Paolo, Janbon Bénédicte, Naciri Bennani Hamza, Rostaing Lionel, Noble Johan
Service de Néphrologie, Hémodialyse, Aphérèses et Transplantation Rénale, Centre Hospitalier Universitaire Grenoble Alpes (CHU), Université Grenoble Alpes, 38043 Grenoble, France.
School of Medicine, Université Grenoble Alpes, 38043 Grenoble, France.
J Clin Med. 2021 Nov 3;10(21):5159. doi: 10.3390/jcm10215159.
Belatacept is a common immunosuppressive therapy used after kidney transplantation (KT) to avoid calcineurin-inhibitor (CNI) use and its related toxicities. It is unclear whether its use exposes KT recipients (KTx) to a greater risk of infection or a poorer response to vaccines. Areas covered: We reviewed PubMed and the Cochrane database. We then summarized the mechanisms and impacts of belatacept use on the risk of infection, particularly opportunistic, in two settings, i.e., de novo KTx and conversion from CNIs. We also focused on COVID-19 infection risk and response to SARS-CoV-2 vaccination in patients whose maintenance immunosuppression relies on belatacept. Expert opinion: When belatacept is used de novo, or after drug conversion the safety profile regarding the risk of infection remains good. However, there is an increased risk of opportunistic infections, mainly CMV disease and Pneumocystis pneumonia, particularly in those with a low eGFR, in older people, in those receiving steroid-based therapy, or those that have an early conversion from CNI to belatacept (i.e., <six months post-transplantation). Thus, we recommend, if possible, delaying conversion from CNI to belatacept until at least six months post-transplantation. Optimal timing seems to be eight months post-transplantation. In addition, KTx receiving belatacept respond poorly to SARS-CoV-2 vaccination.
贝拉西普是肾移植(KT)后常用的免疫抑制疗法,用于避免使用钙调神经磷酸酶抑制剂(CNI)及其相关毒性。目前尚不清楚使用贝拉西普是否会使肾移植受者(KTx)面临更高的感染风险或对疫苗的反应更差。涵盖领域:我们检索了PubMed和Cochrane数据库。然后,我们总结了在两种情况下,即初次肾移植和从CNI转换治疗时,使用贝拉西普对感染风险,特别是机会性感染风险的机制和影响。我们还关注了维持免疫抑制依赖贝拉西普的患者感染新型冠状病毒肺炎(COVID-19)的风险以及对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)疫苗接种的反应。专家意见:当初次使用贝拉西普或药物转换后,感染风险方面的安全性仍然良好。然而,机会性感染的风险增加,主要是巨细胞病毒病和肺孢子菌肺炎,特别是在估算肾小球滤过率(eGFR)低的患者、老年人、接受类固醇治疗的患者或那些从CNI早期转换为贝拉西普的患者(即移植后<6个月)中。因此,我们建议,如果可能的话,将从CNI转换为贝拉西普的时间推迟到至少移植后6个月。最佳时间似乎是移植后8个月。此外,接受贝拉西普治疗的KTx对SARS-CoV-2疫苗接种反应不佳。