Literature DB >> 33131148

Pig kidney xenotransplantation: Progress toward clinical trials.

David K C Cooper1, Hidetaka Hara1, Hayato Iwase1, Takayuki Yamamoto1, Zheng-Yu Wang1, Abhijit Jagdale1, Mohamed H Bikhet1, Huy Q Nguyen1, Jeremy B Foote2, Wayne D Paris3, David Ayares4, Vineeta Kumar5, Douglas J Anderson1, Jayme E Locke1, Devin E Eckhoff1.   

Abstract

Pig organ xenotransplantation offers a solution to the shortage of deceased human organs for transplantation. The pathobiological response to a pig xenograft is complex, involving antibody, complement, coagulation, inflammatory, and cellular responses. To overcome these barriers, genetic manipulation of the organ-source pigs has largely been directed to two major aims-(a) deletion of expression of the known carbohydrate xenoantigens against which humans have natural (preformed) antibodies, and (b) transgenic expression of human protective proteins, for example, complement- and coagulation-regulatory proteins. Conventional (FDA-approved) immunosuppressive therapy is unsuccessful in preventing an adaptive immune response to pig cells, but blockade of the CD40:CD154 costimulation pathway is successful. Survival of genetically engineered pig kidneys in immunosuppressed nonhuman primates can now be measured in months. Non-immunological aspects, for example, pig renal function, a hypovolemia syndrome, and rapid growth of the pig kidney after transplantation, are briefly discussed. We suggest that patients on the wait-list for a deceased human kidney graft who are unlikely to receive one due to long waiting times are those for whom kidney xenotransplantation might first be considered. The potential risk of infection, public attitudes to xenotransplantation, and ethical, regulatory, and financial aspects are briefly addressed.
© 2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  clinical; genetically engineered; kidney; patient selection; pig; xenotransplantation

Mesh:

Year:  2020        PMID: 33131148     DOI: 10.1111/ctr.14139

Source DB:  PubMed          Journal:  Clin Transplant        ISSN: 0902-0063            Impact factor:   2.863


  4 in total

1.  Human IL-17 and TNF-α Additively or Synergistically Regulate the Expression of Proinflammatory Genes, Coagulation-Related Genes, and Tight Junction Genes in Porcine Aortic Endothelial Cells.

Authors:  Weilong Li; Pengfei Chen; Yanli Zhao; Mengtao Cao; Wenjun Hu; Litao Pan; Huimin Sun; Dongsheng Huang; Hanxi Wu; Zhuoheng Song; Huanli Zhong; Lisha Mou; Shaodong Luan; Xiehui Chen; Hanchao Gao
Journal:  Front Immunol       Date:  2022-06-30       Impact factor: 8.786

2.  Production of a Low-Cost, Off-the-Shelf, Decellularized Cartilage Xenograft for Tissue Regeneration.

Authors:  Nicholas A Vernice; Nabih Berri; Ryan J Bender; Xue Dong; Jason A Spector
Journal:  Ann Plast Surg       Date:  2022-05-01       Impact factor: 1.763

Review 3.  Porcine Endogenous Retroviruses and Xenotransplantation, 2021.

Authors:  Joachim Denner
Journal:  Viruses       Date:  2021-10-26       Impact factor: 5.048

4.  Human immune reactivity of GGTA1/CMAH/A3GALT2 triple knockout Yucatan miniature pigs.

Authors:  Joohyun Shim; Nayoung Ko; Hyoung-Joo Kim; Yongjin Lee; Jeong-Woong Lee; Dong-Il Jin; Hyunil Kim; Kimyung Choi
Journal:  Transgenic Res       Date:  2021-07-07       Impact factor: 2.788

  4 in total

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