» Articles » PMID: 34553390

Initial Experimental Experience of Triple-knockout Pig Red Blood Cells As Potential Sources for Transfusion in Alloimmunized Patients with Sickle Cell Disease

Overview
Journal Transfusion
Specialty Hematology
Date 2021 Sep 23
PMID 34553390
Citations 8
Authors
Affiliations
Soon will be listed here.
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 In an in vivo study, after an estimated 25% of blood volume was withdrawn from two capuchin monkeys, CFSE-labeled TKO pRBCs were transfused. Loss of TKO pRBCs was monitored by flow cytometry, and 7 weeks later, 25% of blood was withdrawn, and CFSE-labeled monkey RBCs were transfused.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.

Citing Articles

Generation and characterization of genetically modified pigs with GGTA1/β4GalNT2/CMAH knockout and human CD55/CD47 expression for xenotransfusion studies.

Fang B, Wang C, Yuan Y, Liu X, Shi L, Li L Sci Rep. 2024; 14(1):29870.

PMID: 39622959 PMC: 11612173. DOI: 10.1038/s41598-024-81730-2.


Investigation of the efficacy and safety of wild- type and triple-gene knockout pig RBC transfusions in nonhuman primates.

Roh J, Hwang J, Park S, Lee H, Park E, Lee H Front Immunol. 2024; 15:1418249.

PMID: 38994362 PMC: 11236543. DOI: 10.3389/fimmu.2024.1418249.


Initial investigation on the feasibility of porcine red blood cells from genetically modified pigs as an alternative to human red blood cells for transfusion.

Park S, Lee H, Park E, Roh J, Kang P, Shim J Front Immunol. 2023; 14:1298035.

PMID: 38035112 PMC: 10682702. DOI: 10.3389/fimmu.2023.1298035.


In vitro and in vivo immune assessments of genetically-engineered pig skin grafts in New World (squirrel) monkeys.

Hara H, Foote J, Hansen-Estruch C, Bikhet M, Nguyen H, Javed M Xenotransplantation. 2023; 30(6):e12832.

PMID: 37870485 PMC: 10843142. DOI: 10.1111/xen.12832.


Future prospects for the clinical transfusion of pig red blood cells.

Chornenkyy Y, Yamamoto T, Hara H, Stowell S, Ghiran I, Robson S Blood Rev. 2023; 61:101113.

PMID: 37474379 PMC: 10968389. DOI: 10.1016/j.blre.2023.101113.


References
1.
Katz D, White S, Huang W, Kumar R, Christianson D . Structure determination of aquomet porcine hemoglobin at 2.8 A resolution. J Mol Biol. 1994; 244(5):541-53. DOI: 10.1006/jmbi.1994.1751. View

2.
Cooper D, Hara H, Yazer M . Genetically engineered pigs as a source for clinical red blood cell transfusion. Clin Lab Med. 2010; 30(2):365-80. DOI: 10.1016/j.cll.2010.02.001. View

3.
Yamamoto T, Hara H, Iwase H, Jagdale A, Bikhet M, Morsi M . The final obstacle to successful pre-clinical xenotransplantation?. Xenotransplantation. 2020; 27(5):e12596. DOI: 10.1111/xen.12596. View

4.
Yamamoto T, Hara H, Foote J, Wang L, Li Q, Klein E . Life-supporting Kidney Xenotransplantation From Genetically Engineered Pigs in Baboons: A Comparison of Two Immunosuppressive Regimens. Transplantation. 2019; 103(10):2090-2104. DOI: 10.1097/TP.0000000000002796. View

5.
Ribeil J, Hacein-Bey-Abina S, Payen E, Magnani A, Semeraro M, Magrin E . Gene Therapy in a Patient with Sickle Cell Disease. N Engl J Med. 2017; 376(9):848-855. DOI: 10.1056/NEJMoa1609677. View