Complement-targeting therapeutics for ischemia-reperfusion injury in transplantation and the potential for ex vivo delivery

被引:10
|
作者
Delaura, Isabel F. F. [1 ]
Gao, Qimeng [1 ]
Anwar, Imran J. J. [1 ]
Abraham, Nader [1 ]
Kahan, Riley [1 ]
Hartwig, Matthew G. G. [2 ]
Barbas, Andrew S. S. [1 ]
机构
[1] Duke Univ, Sch Med, Dept Surg, Durham, NC 27708 USA
[2] Duke Univ, Med Ctr, Div Cardiovasc & Thorac Surg, Durham, NC USA
来源
FRONTIERS IN IMMUNOLOGY | 2022年 / 13卷
关键词
complement inhibitor; ischemia-reperfusion injury; ex vivo delivery; organ transplantation; classic pathway; ANTIBODY-MEDIATED REJECTION; DELAYED GRAFT FUNCTION; DONOR BRAIN-DEATH; ATTENUATES LIVER ISCHEMIA; C5A RECEPTOR ANTAGONIST; C1 ESTERASE INHIBITOR; ISCHEMIA/REPERFUSION INJURY; COLD ISCHEMIA; KIDNEY-TRANSPLANTATION; DOUBLE-BLIND;
D O I
10.3389/fimmu.2022.1000172
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Organ shortages and an expanding waitlist have led to increased utilization of marginal organs. All donor organs are subject to varying degrees of IRI during the transplant process. Extended criteria organs, including those from older donors and organs donated after circulatory death are especially vulnerable to ischemia-reperfusion injury (IRI). Involvement of the complement cascade in mediating IRI has been studied extensively. Complement plays a vital role in the propagation of IRI and subsequent recruitment of the adaptive immune elements. Complement inhibition at various points of the pathway has been shown to mitigate IRI and minimize future immune-mediated injury in preclinical models. The recent introduction of ex vivo machine perfusion platforms provides an ideal window for therapeutic interventions. Here we review the role of complement in IRI by organ system and highlight potential therapeutic targets for intervention during ex vivo machine preservation of donor organs.
引用
收藏
页数:11
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