Xeno kidney: revolutionizing kidney disease treatment.

Frontiers in nephrology Pub Date : 2026-02-20 eCollection Date: 2026-01-01 DOI:10.3389/fneph.2026.1707170
Diksha Makkar, Diksha Gakhar, Aruna Rakha
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Abstract

The prevalence of end-stage kidney failure has been exponentially increasing, leading to a gross mismatch between the number of patients who may benefit from transplantation and the limited supply of suitable donor organs. As renal transplantation remains a viable and the most effective option for end-stage kidney disease, the fact remains that the availability of eligible human donor organs is highly unlikely to meet the projected demand. This undermines the need for alternative strategies, including therapies and the development of transplant substitutes. In this context, xenotransplantation has emerged as a lucrative avenue for patients with renal failure who struggle to obtain a suitable graft promptly. The pig is currently the most preferred animal donor for kidney due to its physiological analogy to humans. Nevertheless, xenotransplantation is associated with certain complications as well, which broadly include the risk of hyperacute rejection mediated by preexisting antibodies to xenogeneic antigens, the stimulation of innate immune responses, and thereby the possibility of chronic rejection. Recent advances in xenotransplantation research have offered hope in overcoming these roadblocks and transforming the field of nephrology in the coming years. Genetic engineering has enabled creating low-immunogenicity grafts from donor pigs, including GalTKO (lacking α-Gal epitopes/galactose-α-1,3-galactose knockout) and gene knockouts that limit the complement system activation and clot formation. Furthermore, advances in immunosuppressive regimens, such as co-stimulation blockade and anti-complement treatment, hold great promise for xenograft acceptance and long-term results. In addition, numerous strategies are being explored to induce tolerance, such as mixed chimerism or regulatory T-cell therapy, to achieve a condition of acceptable graft tolerance without dependency on lifelong immunosuppressive treatments. Collectively, these developments support the translational potential of xenotransplantation as a stand-alone treatment or as an adjunct to standard renal replacement therapies. Despite the setbacks, ongoing preclinical research and early clinical trials are expected to refine the safety, durability, and clinical applicability in a xenotransplantation setting.

Xeno肾脏:革命性的肾脏疾病治疗。
终末期肾衰竭的发病率呈指数级增长,导致可能受益于移植的患者数量与合适的供体器官供应有限之间的严重不匹配。由于肾移植仍然是治疗终末期肾病的可行和最有效的选择,但事实仍然是,符合条件的人类供体器官的可用性极不可能满足预计的需求。这削弱了对替代策略的需求,包括治疗和移植替代品的开发。在这种情况下,异种移植已经成为肾衰竭患者的一个有利可图的途径,他们努力迅速获得合适的移植物。猪是目前最受欢迎的动物肾脏供体,因为它在生理上与人类相似。然而,异种移植也与某些并发症有关,其中广泛包括由预先存在的针对异种抗原的抗体介导的超急性排斥反应的风险,先天免疫反应的刺激,从而可能出现慢性排斥反应。异种移植研究的最新进展为克服这些障碍并在未来几年改变肾脏病学领域提供了希望。基因工程已经能够从供体猪中创建低免疫原性移植物,包括GalTKO(缺乏α-Gal表位/半乳糖-α-1,3-半乳糖敲除)和限制补体系统激活和凝块形成的基因敲除。此外,免疫抑制方案的进展,如共刺激阻断和抗补体治疗,对异种移植物的接受和长期效果有很大的希望。此外,正在探索许多策略来诱导耐受性,如混合嵌合或调节性t细胞治疗,以达到可接受的移植物耐受性条件,而不依赖终身免疫抑制治疗。总的来说,这些进展支持异种移植作为独立治疗或作为标准肾脏替代疗法的辅助治疗的转化潜力。尽管遇到挫折,但正在进行的临床前研究和早期临床试验有望改善异种移植环境中的安全性、持久性和临床适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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