Literature DB >> 34553390

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

Takayuki Yamamoto1,2, Mohamed H Bikhet1, Marisa B Marques3, Huy Q Nguyen1, Yehua Cui1, Mariyam Javed1, Syed Sikandar Raza1, David Ayares4, Hayato Iwase1, David K C Cooper1, Hidetaka Hara1.   

Abstract

BACKGROUND: Blood transfusion remains important in the treatment of patients with sickle cell disease (SCD). However, alloimmunization after blood transfusion is associated with patient morbidity and mortality. Triple-knockout (TKO) pigs (i.e., pigs in which the three known xenoantigens to which humans have anti-pig antibodies have been deleted) may be an alternative source of RBCs for these patients because many humans have no preformed antibodies to TKO pig RBCs (pRBCs). METHODS AND MATERIALS: In an in vitro study, plasma from alloimmunized (n = 12) or non-alloimmunized (n = 12) SCD patients was used to determine IgM/IgG binding to, and CDC of, TKO pRBCs. In an in vivo study, after an estimated 25% of blood volume was withdrawn from two capuchin monkeys, CFSE-labeled TKO pRBCs were transfused. Loss of TKO pRBCs was monitored by flow cytometry, and 7 weeks later, 25% of blood was withdrawn, and CFSE-labeled monkey RBCs were transfused.
RESULTS: The in vitro study demonstrated that plasma from neither alloimmunized nor non-alloimmunized SCD patients bound IgM/IgG to, or induced CDC of, TKO pRBCs. In the in vivo study, survival of TKO pRBCs in the two capuchin monkeys was of 5 and 7 days, respectively, whereas after allotransfusion, survival was >28 days.
CONCLUSIONS: In conclusion, (1) in the present limited study, no antibodies were detected that cross-reacted with TKO pRBCs, and (2) TKO pigs may possibly be an alternate source of RBCs in an emergency if no human RBCs are available.
© 2021 AABB.

Entities:  

Keywords:  capuchin monkeys; red blood cells; sickle cell disease; triple-knockout pigs; xenotransfusion

Mesh:

Substances:

Year:  2021        PMID: 34553390      PMCID: PMC9027667          DOI: 10.1111/trf.16667

Source DB:  PubMed          Journal:  Transfusion        ISSN: 0041-1132            Impact factor:   3.157


  29 in total

1.  The problem of the "4th xenoantigen" after pig organ transplantation in non-human primates may be overcome by expression of human "protective" proteins.

Authors:  Takayuki Yamamoto; Hidetaka Hara; David Ayares; David K C Cooper
Journal:  Xenotransplantation       Date:  2020-11-01       Impact factor: 3.907

2.  Life-supporting Kidney Xenotransplantation From Genetically Engineered Pigs in Baboons: A Comparison of Two Immunosuppressive Regimens.

Authors:  Takayuki Yamamoto; Hidetaka Hara; Jeremy Foote; Liaoran Wang; Qi Li; Edwin C Klein; Hendrik Jan Schuurman; Hongmin Zhou; Juan Li; A Joseph Tector; Zhongqiang Zhang; Mohamed Ezzelarab; Ray Lovingood; David Ayares; Devin E Eckhoff; David K C Cooper; Hayato Iwase
Journal:  Transplantation       Date:  2019-10       Impact factor: 4.939

3.  Gene Therapy in a Patient with Sickle Cell Disease.

Authors:  Jean-Antoine Ribeil; Salima Hacein-Bey-Abina; Emmanuel Payen; Alessandra Magnani; Michaela Semeraro; Elisa Magrin; Laure Caccavelli; Benedicte Neven; Philippe Bourget; Wassim El Nemer; Pablo Bartolucci; Leslie Weber; Hervé Puy; Jean-François Meritet; David Grevent; Yves Beuzard; Stany Chrétien; Thibaud Lefebvre; Robert W Ross; Olivier Negre; Gabor Veres; Laura Sandler; Sandeep Soni; Mariane de Montalembert; Stéphane Blanche; Philippe Leboulch; Marina Cavazzana
Journal:  N Engl J Med       Date:  2017-03-02       Impact factor: 91.245

4.  The final obstacle to successful pre-clinical xenotransplantation?

Authors:  Takayuki Yamamoto; Hidetaka Hara; Hayato Iwase; Abhijit Jagdale; Mohamed H Bikhet; Mahmoud A Morsi; Yehua Cui; Huy Q Nguyen; Zheng-Yu Wang; Douglas J Anderson; Jeremy Foote; Henk-Jan Schuurman; David Ayares; Devin E Eckhoff; David K C Cooper
Journal:  Xenotransplantation       Date:  2020-06-25       Impact factor: 3.907

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

Authors:  David K C Cooper; Hidetaka Hara; Mark Yazer
Journal:  Clin Lab Med       Date:  2010-05-06       Impact factor: 1.935

6.  Genetically engineered pig red blood cells for clinical transfusion: initial in vitro studies.

Authors:  Cassandra Long; Hidetaka Hara; Zachary Pawlikowski; Naoko Koike; Thomas d'Arville; Peter Yeh; Mohamed Ezzelarab; David Ayares; Mark Yazer; David K C Cooper
Journal:  Transfusion       Date:  2009-07-14       Impact factor: 3.157

7.  Structure determination of aquomet porcine hemoglobin at 2.8 A resolution.

Authors:  D S Katz; S P White; W Huang; R Kumar; D W Christianson
Journal:  J Mol Biol       Date:  1994-12-16       Impact factor: 5.469

8.  Initial investigation of the potential of modified porcine erythrocytes for transfusion in primates.

Authors:  Jan M Eckermann; Leo H Buhler; Alex Zhu; Frank J M F Dor; Michel Awwad; David K C Cooper
Journal:  Xenotransplantation       Date:  2004-01       Impact factor: 3.907

9.  Cardiac xenografts between primate species provide evidence for the importance of the alpha-galactosyl determinant in hyperacute rejection.

Authors:  B H Collins; A H Cotterell; K R McCurry; C G Alvarado; J C Magee; W Parker; J L Platt
Journal:  J Immunol       Date:  1995-05-15       Impact factor: 5.422

10.  Xenoantigen Deletion and Chemical Immunosuppression Can Prolong Renal Xenograft Survival.

Authors:  Andrew B Adams; Steven C Kim; Gregory R Martens; Joseph M Ladowski; Jose L Estrada; Luz M Reyes; Cindy Breeden; Allison Stephenson; Devin E Eckhoff; Matt Tector; Alfred Joseph Tector
Journal:  Ann Surg       Date:  2018-10       Impact factor: 12.969

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