Literature DB >> 20513556

Genetically engineered pigs as a source for clinical red blood cell transfusion.

David K C Cooper1, Hidetaka Hara, Mark Yazer.   

Abstract

The transfusion of animal blood or red blood cells (RBCs) into humans goes back to 1667, and the practice persisted until the early 1900s. In recent years, in part because of the shortage of acceptable and safe human blood worldwide, there has been renewed interest in the possibility of using genetically-engineered pigs as sources of RBCs for clinical transfusion. Pigs are becoming available in which the cells, tissues, and organs are to some extent protected from the human immune response. This extends significant protection from antibody-mediated complement lysis. Transfusion of these RBCs into nonhuman primates, however, indicates that they are rapidly lost from the circulation, almost certainly through the phagocytic activity of macrophages. Further genetic manipulation may resolve this problem. In view of the potential advantages of pig RBCs with regard to the absence of infectious microorganisms and the rapid progress being made in genetically modifying pigs, pig RBCs may eventually become a feasible source of blood for clinical transfusion. Copyright (c) 2010 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20513556     DOI: 10.1016/j.cll.2010.02.001

Source DB:  PubMed          Journal:  Clin Lab Med        ISSN: 0272-2712            Impact factor:   1.935


  9 in total

1.  A brief history of cross-species organ transplantation.

Authors:  David K C Cooper
Journal:  Proc (Bayl Univ Med Cent)       Date:  2012-01

2.  Erythrocytes from GGTA1/CMAH knockout pigs: implications for xenotransfusion and testing in non-human primates.

Authors:  Zheng-Yu Wang; Christopher Burlak; Jose L Estrada; Ping Li; Matthew F Tector; A Joseph Tector
Journal:  Xenotransplantation       Date:  2014-07-02       Impact factor: 3.907

3.  Impact of Laser Power and Firing Angle on Coagulation Efficiency in Laser Treatment for Twin-Twin Transfusion Syndrome: An ex vivo Placenta Study.

Authors:  Joost Akkermans; Loes van der Donk; Suzanne H P Peeters; Sjoerd van Tuijl; Johanna M Middeldorp; Enrico Lopriore; Dick Oepkes
Journal:  Fetal Diagn Ther       Date:  2017-03-29       Impact factor: 2.587

Review 4.  Genetically-engineered pigs as sources for clinical red blood cell transfusion: What pathobiological barriers need to be overcome?

Authors:  Benjamin Smood; Hidetaka Hara; Leah J Schoel; David K C Cooper
Journal:  Blood Rev       Date:  2019-01-28       Impact factor: 8.250

Review 5.  Xenotransplantation-the current status and prospects.

Authors:  D K C Cooper; R Gaston; D Eckhoff; J Ladowski; T Yamamoto; L Wang; H Iwase; H Hara; M Tector; A J Tector
Journal:  Br Med Bull       Date:  2018-03-01       Impact factor: 4.291

6.  Initial experimental experience of triple-knockout pig red blood cells as potential sources for transfusion in alloimmunized patients with sickle cell disease.

Authors:  Takayuki Yamamoto; Mohamed H Bikhet; Marisa B Marques; Huy Q Nguyen; Yehua Cui; Mariyam Javed; Syed Sikandar Raza; David Ayares; Hayato Iwase; David K C Cooper; Hidetaka Hara
Journal:  Transfusion       Date:  2021-09-22       Impact factor: 3.157

Review 7.  Progress in pig-to-non-human primate transplantation models (1998-2013): a comprehensive review of the literature.

Authors:  David K C Cooper; Vikas Satyananda; Burcin Ekser; Dirk J van der Windt; Hidetaka Hara; Mohamed B Ezzelarab; Henk-Jan Schuurman
Journal:  Xenotransplantation       Date:  2014-09-01       Impact factor: 3.907

Review 8.  Modifying the sugar icing on the transplantation cake.

Authors:  David K C Cooper
Journal:  Glycobiology       Date:  2016-03-01       Impact factor: 4.313

9.  Anti-Neu5Gc and anti-non-Neu5Gc antibodies in healthy humans.

Authors:  Bingsi Gao; Cassandra Long; Whayoung Lee; Zhongqiang Zhang; Xiaotian Gao; Doug Landsittel; Mohamed Ezzelarab; David Ayares; Yuliang Huang; David K C Cooper; Yi Wang; Hidetaka Hara
Journal:  PLoS One       Date:  2017-07-17       Impact factor: 3.240

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.