University of Minnesota School of Medicine, Minneapolis MN.
Emory School of Medicine, Atlanta GA.
Ann Surg. 2021 Sep 1;274(3):473-480. doi: 10.1097/SLA.0000000000004996.
Pig-to-primate renal xenotransplantation is plagued by early antibody-mediated graft loss which precludes clinical application of renal xenotransplantation. We evaluated whether temporary complement inhibition with anti-C5 antibody Tesidolumab could minimize the impact of early antibody-mediated rejection in rhesus monkeys receiving pig kidneys receiving costimulatory blockade-based immunosuppression.
Double (Gal and Sda) and triple xenoantigen (Gal, Sda, and SLA I) pigs were created using CRISPR/Cas. Kidneys from DKO and TKO pigs were transplanted into rhesus monkeys that had the least reactive crossmatches. Recipients received anti-C5 antibody weekly for 70 days, and T cell depletion, anti-CD154, mycophenolic acid, and steroids as baseline immunosuppression (n = 7). Control recipients did not receive anti-C5 therapy (n = 10).
Temporary anti-C5 therapy reduced early graft loss secondary to antibody-mediated rejection and improved graft survival (P < 0.01). Deleting class I MHC (SLA I) in donor pigs did not ameliorate early antibody-mediated rejection (table). Anti-C5 therapy did not allow for the use of tacrolimus instead of anti-CD154 (table), prolonging survival to a maximum of 62 days.
Inhibition of the C5 complement subunit prolongs renal xenotransplant survival in a pig to non-human primate model.
猪到灵长类动物的肾脏异种移植受到早期抗体介导的移植物排斥的困扰,这使得肾脏异种移植无法应用于临床。我们评估了抗 C5 抗体 Tesidolumab 的临时补体抑制作用是否可以最小化接受基于共刺激阻断的免疫抑制的恒河猴接受猪肾后早期抗体介导排斥的影响。
使用 CRISPR/Cas 技术创建了双重(Gal 和 Sda)和三重异种抗原(Gal、Sda 和 SLA I)猪。来自 DKO 和 TKO 猪的肾脏被移植到交叉配型反应性最低的恒河猴体内。受者每周接受抗 C5 抗体治疗 70 天,并接受 T 细胞耗竭、抗 CD154、霉酚酸和类固醇作为基础免疫抑制(n = 7)。对照受者未接受抗 C5 治疗(n = 10)。
临时抗 C5 治疗减少了抗体介导的排斥反应引起的早期移植物丢失,提高了移植物存活率(P < 0.01)。在供体猪中删除 I 类 MHC(SLA I)并没有改善早期抗体介导的排斥反应(表)。抗 C5 治疗不能允许使用他克莫司代替抗 CD154(表),将存活时间延长至最长 62 天。
抑制 C5 补体亚单位可延长猪到灵长类动物模型中的肾脏异种移植的存活时间。