Suppr超能文献

巴利昔单抗治疗肾移植后钙调磷酸酶抑制剂治疗失败后的挽救性免疫抑制。

Abatacept as rescue immunosuppression after calcineurin inhibitor treatment failure in renal transplantation.

机构信息

Emory Transplant Center, Atlanta, Georgia.

Department of Pathology & Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia.

出版信息

Am J Transplant. 2019 Aug;19(8):2342-2349. doi: 10.1111/ajt.15319. Epub 2019 Mar 12.

Abstract

A majority of kidney transplant recipients receive calcineurin inhibitor-based immunosuppression. However, some do not tolerate calcineurin inhibitors and require other immunosuppressive strategies. Until recently, alternative approaches have been associated with inferior outcomes, but recent methods have effectively utilized belatacept in calcineurin inhibitor-intolerant patients. Though promising, belatacept uptake has been limited by higher acute rejection rates, unavailability due to production shortages, and logistical challenges as a result of intravenous infusion requirements. Interestingly, its predecessor abatacept is clinically available in subcutaneous formulation to treat autoimmune disorders but has not been used in clinical transplantation. Here we report on a series of 9 calcineurin inhibitor-intolerant transplant recipients converted to abatacept early after transplant as rescue immunosuppression during periods of belatacept unavailability. Retrospective review revealed successful allograft salvage and 100% patient and graft survival (median 115 months) after conversion to abatacept. Patients received abatacept for a median duration of 82 months with stable, long-term renal allograft function, a single cellular rejection episode, and no clinically apparent protective immunity concerns. Hence our findings suggest that future clinical studies utilizing abatacept either de novo or as conversion therapy in transplant recipients should be considered.

摘要

大多数肾移植受者接受钙调神经磷酸酶抑制剂为基础的免疫抑制治疗。然而,有些受者不能耐受钙调神经磷酸酶抑制剂,需要其他免疫抑制策略。直到最近,替代方法的结果都较差,但最近的方法已经有效地将贝利尤单抗用于不能耐受钙调神经磷酸酶抑制剂的患者。虽然前景广阔,但由于急性排斥反应率较高、因生产短缺而无法获得以及静脉输注要求导致的后勤挑战,贝利尤单抗的应用受到限制。有趣的是,其前体阿巴西普在临床上可用于治疗自身免疫性疾病的皮下制剂,但尚未在临床移植中使用。在这里,我们报告了一系列 9 例钙调神经磷酸酶抑制剂不耐受的移植受者,在贝利尤单抗无法获得期间,作为挽救性免疫抑制,在移植后早期转换为阿巴西普。回顾性研究显示,在转换为阿巴西普后,成功挽救了移植物,患者和移植物的存活率为 100%(中位数 115 个月)。患者接受阿巴西普治疗的中位时间为 82 个月,其肾功能稳定,长期稳定,仅有一次细胞性排斥反应,且无明显的临床保护性免疫问题。因此,我们的研究结果表明,未来的临床研究应该考虑在移植受者中使用阿巴西普,无论是作为初始治疗还是转换治疗。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验