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Production of Feline Universal Erythrocytes with Methoxy Polyethylene Glycol
Blood group mismatch in veterinary medicine is a significant problem in blood transfusion, sometimes leading to severe transfusion reactions and even patient death. Blood groups vary from species to species and there are three known blood groups in cats: A, B and AB. While A-type cats are most commo...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10532140/ https://www.ncbi.nlm.nih.gov/pubmed/37754890 http://dx.doi.org/10.3390/jfb14090476 |
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author | Kim, Hyung Kyu Ahn, Dan Bi Jang, Han Byeol Ma, Jing Xing, Juping Yoon, Joo Won Lee, Kyung Hee Lee, Dong Min Kim, Chang Hyun Kim, Hee Young |
author_facet | Kim, Hyung Kyu Ahn, Dan Bi Jang, Han Byeol Ma, Jing Xing, Juping Yoon, Joo Won Lee, Kyung Hee Lee, Dong Min Kim, Chang Hyun Kim, Hee Young |
author_sort | Kim, Hyung Kyu |
collection | PubMed |
description | Blood group mismatch in veterinary medicine is a significant problem in blood transfusion, sometimes leading to severe transfusion reactions and even patient death. Blood groups vary from species to species and there are three known blood groups in cats: A, B and AB. While A-type cats are most common, there is a shortage of feline B-type blood groups in cats. By using methoxy polyethylene glycol (mPEG) to protect antigenic epitopes on red blood cells (RBCs), we aimed to find the optimal conditions for the production of feline universal RBCs. The surfaces of feline A-type RBCs were treated with mPEG at various molecular weights and concentrations. Agglutination tests showed that the coating of feline A-type RBCs with mPEG of 20 kDa and 2 mM blocked hemagglutination to feline anti-A alloantibodies over 8 h. While no differences in RBC size and shape between intact and mPEG-treated RBCs were seen, coating RBCs with mPEG inhibited the binding of feline anti-A alloantibodies. Furthermore, the mPEG-treated RBCs did not cause spontaneous hemolysis or osmotic fragility, compared to control RBCs. According to a monocyte monolayer assay, mPEG treatment significantly reduced feline anti-A antibody-mediated phagocystosis of RBCs. These results confirm the potential of using activated mPEG on feline A-type RBC to create universal erythrocytes for transfusion to B-type cats. |
format | Online Article Text |
id | pubmed-10532140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105321402023-09-28 Production of Feline Universal Erythrocytes with Methoxy Polyethylene Glycol Kim, Hyung Kyu Ahn, Dan Bi Jang, Han Byeol Ma, Jing Xing, Juping Yoon, Joo Won Lee, Kyung Hee Lee, Dong Min Kim, Chang Hyun Kim, Hee Young J Funct Biomater Article Blood group mismatch in veterinary medicine is a significant problem in blood transfusion, sometimes leading to severe transfusion reactions and even patient death. Blood groups vary from species to species and there are three known blood groups in cats: A, B and AB. While A-type cats are most common, there is a shortage of feline B-type blood groups in cats. By using methoxy polyethylene glycol (mPEG) to protect antigenic epitopes on red blood cells (RBCs), we aimed to find the optimal conditions for the production of feline universal RBCs. The surfaces of feline A-type RBCs were treated with mPEG at various molecular weights and concentrations. Agglutination tests showed that the coating of feline A-type RBCs with mPEG of 20 kDa and 2 mM blocked hemagglutination to feline anti-A alloantibodies over 8 h. While no differences in RBC size and shape between intact and mPEG-treated RBCs were seen, coating RBCs with mPEG inhibited the binding of feline anti-A alloantibodies. Furthermore, the mPEG-treated RBCs did not cause spontaneous hemolysis or osmotic fragility, compared to control RBCs. According to a monocyte monolayer assay, mPEG treatment significantly reduced feline anti-A antibody-mediated phagocystosis of RBCs. These results confirm the potential of using activated mPEG on feline A-type RBC to create universal erythrocytes for transfusion to B-type cats. MDPI 2023-09-18 /pmc/articles/PMC10532140/ /pubmed/37754890 http://dx.doi.org/10.3390/jfb14090476 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kim, Hyung Kyu Ahn, Dan Bi Jang, Han Byeol Ma, Jing Xing, Juping Yoon, Joo Won Lee, Kyung Hee Lee, Dong Min Kim, Chang Hyun Kim, Hee Young Production of Feline Universal Erythrocytes with Methoxy Polyethylene Glycol |
title | Production of Feline Universal Erythrocytes with Methoxy Polyethylene Glycol |
title_full | Production of Feline Universal Erythrocytes with Methoxy Polyethylene Glycol |
title_fullStr | Production of Feline Universal Erythrocytes with Methoxy Polyethylene Glycol |
title_full_unstemmed | Production of Feline Universal Erythrocytes with Methoxy Polyethylene Glycol |
title_short | Production of Feline Universal Erythrocytes with Methoxy Polyethylene Glycol |
title_sort | production of feline universal erythrocytes with methoxy polyethylene glycol |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10532140/ https://www.ncbi.nlm.nih.gov/pubmed/37754890 http://dx.doi.org/10.3390/jfb14090476 |
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