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预防 T 细胞对猪异种移植物的排斥。

Preventing T cell rejection of pig xenografts.

机构信息

Emory Transplant Center, Emory University School of Medicine, Atlanta, GA, USA.

Emory Transplant Center, Emory University School of Medicine, Atlanta, GA, USA.

出版信息

Int J Surg. 2015 Nov;23(Pt B):285-290. doi: 10.1016/j.ijsu.2015.07.722. Epub 2015 Aug 22.

Abstract

Xenotransplantation is a potential solution to the limited supply of donor organs. While early barriers to xenograft acceptance, such as hyperacute rejection, are now largely avoided through genetic engineering, the next frontier in successful xenograft survival will require prevention of T cell-mediated rejection. Most successful immunosuppressive regimens in xenotransplantation utilize T cell depletion with antibody therapy. Additionally, the use of T cell costimulatory blockade - specifically blockade of the CD40-CD154 pathway - shows promise with several reports of long-term xenograft survival. Additional therapies, such as transgenic expression of T cell coinhibitory molecules or transfer of immunomodulatory cells to promote tolerance, may be necessary to achieve reliable long-term xenograft acceptance. Further studies in pre-clinical models are essential in order to optimize these regimens prior to trials in patients.

摘要

异种移植是解决供体器官有限供应的一种潜在方法。虽然通过基因工程,异种移植物接受的早期障碍,如超急性排斥反应,现在在很大程度上得到了避免,但成功的异种移植物存活的下一个前沿领域将需要预防 T 细胞介导的排斥反应。异种移植中大多数成功的免疫抑制方案都利用抗体疗法进行 T 细胞耗竭。此外,使用 T 细胞共刺激阻断 - 特别是阻断 CD40-CD154 途径 - 显示出有希望的前景,有几项关于长期异种移植物存活的报告。其他疗法,如 T 细胞共抑制分子的转基因表达或免疫调节细胞的转移以促进耐受,可能是实现可靠的长期异种移植物接受所必需的。为了在患者试验之前优化这些方案,在临床前模型中进行进一步的研究是至关重要的。

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