Pig-to-human heart transplantation: Who goes first?

被引:23
|
作者
Pierson, Richard N., III [1 ,2 ]
Burdorf, Lars [1 ,2 ]
Madsen, Joren C. [1 ,2 ]
Lewis, Gregory D. [3 ]
D'Alessandro, David A. [1 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Div Cardiac Surg, Boston, MA 02115 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Dept Surg, Ctr Transplantat Sci, Boston, MA 02115 USA
[3] Harvard Univ, Massachusetts Gen Hosp, Dept Med, Div Cardiol, Boston, MA 02115 USA
关键词
alloantibody; allosensitization; alloimmunity; cardiac allograft vasculopathy; cardiac; heart transplant; alternatives; chronic rejection; ethics and public policy; heart failure; mechanical circulatory support; translational research; science; xenotransplantation; INTERNATIONAL SOCIETY; LUNG TRANSPLANTATION; RENAL-TRANSPLANT; SWINE; XENOTRANSPLANTATION; ALLOSENSITIZATION; ANTIBODIES; SURVIVAL; RISK;
D O I
10.1111/ajt.15916
中图分类号
R61 [外科手术学];
学科分类号
摘要
Cardiac xenotransplantation has recently taken an important step towards clinical reality. In anticipation of the "first-in-human" heart xenotransplantation trial, we propose a set of patient characteristics that define potential candidates. Our premise is that, to be ethically justified, the risks posed by current state-of-the-art options must outweigh the anticipated risks of a pioneering xenotransplant procedure. Suitable candidates include patients who are at high immunologic risk because of sensitization to alloantigens, including those who have exhibited early onset or accelerated cardiac allograft vasculopathy. In addition, patients should be considered (1) for whom mechanical circulatory support would be prohibitively risky due to a hypercoagulable state, a contraindication to anticoagulation, or restrictive physiology; (2) with severe biventricular dysfunction predicting unsuccessful univentricular left heart support; and (3) adults with complex congenital heart disease. In conclusion, because the published preclinical benchmark for clinical translation of heart xenotransplantation appears within reach, carefully and deliberately defining appropriate trial participants is timely as the basis for ethical clinical trial design.
引用
收藏
页码:2669 / 2674
页数:6
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