Pig kidney graft survival in a baboon for 136days: longest life-supporting organ graft survival to date

被引:186
作者
Iwase, Hayato [1 ]
Liu, Hong [1 ,2 ]
Wijkstrom, Martin [1 ]
Zhou, Huidong [1 ,3 ]
Singh, Jagjit [1 ]
Hara, Hidetaka [1 ]
Ezzelarab, Mohamed [1 ]
Long, Cassandra [1 ]
Klein, Edwin [4 ]
Wagner, Robert [4 ]
Phelps, Carol [5 ]
Ayares, David [5 ]
Shapiro, Ron [1 ]
Humar, Abhinav [1 ]
Cooper, David K. C. [1 ]
机构
[1] Univ Pittsburgh, Thomas E Starzl Transplantat Inst, Pittsburgh, PA 15261 USA
[2] Shanxi Med Univ, Dept Gen Surg, Hosp 1, Taiyuan, Shanxi, Peoples R China
[3] Univ South China, Affiliated Hosp 2, Ctr Kidney Transplantat, Hengyang, Hunan, Peoples R China
[4] Univ Pittsburgh, Div Lab Anim Resources, Pittsburgh, PA 15261 USA
[5] Revivicor, Blacksburg, VA USA
关键词
anti-IL-6R antagonist; costimulation blockade; genetically engineered; kidney; pig; xenotransplantation; XENOGRAFT SURVIVAL; XENOTRANSPLANTATION; TRANSPLANTATION; EXPERIENCE; ACTIVATION; RECIPIENTS; PROGRESS;
D O I
10.1111/xen.12174
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The longest survival of a non-human primate with a life-supporting kidney graft to date has been 90days, although graft survival >30days has been unusual. A baboon received a kidney graft from an -1,3-galactosyltransferase gene-knockout pig transgenic for two human complement-regulatory proteins and three human coagulation-regulatory proteins (although only one was expressed in the kidney). Immunosuppressive therapy was with ATG+anti-CD20mAb (induction) and anti-CD40mAb+rapamycin+corticosteroids (maintenance). Anti-TNF- and anti-IL-6R were administered. The baboon survived 136days with a generally stable serum creatinine (0.6 to 1.6mg/dl) until termination. No features of a consumptive coagulopathy (e.g., thrombocytopenia, decreased fibrinogen) or of a protein-losing nephropathy were observed. There was no evidence of an elicited anti-pig antibody response. Death was from septic shock (Myroides spp). Histology of a biopsy on day 103 was normal, but by day 136, the kidney showed features of glomerular enlargement, thrombi, and mesangial expansion. The combination of (i) a graft from a specific genetically engineered pig, (ii) an effective immunosuppressive regimen, and (iii) anti-inflammatory agents prevented immune injury and a protein-losing nephropathy, and delayed coagulation dysfunction. This outcome encourages us that clinical renal xenotransplantation may become a reality.
引用
收藏
页码:302 / 309
页数:8
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