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Production of Feline Universal Erythrocytes with Methoxy Polyethylene Glycol

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dc.contributor.author김희영-
dc.date.accessioned2023-11-07T07:57:49Z-
dc.date.available2023-11-07T07:57:49Z-
dc.date.issued2023-09-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/196563-
dc.description.abstractBlood 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.-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfJOURNAL OF FUNCTIONAL BIOMATERIALS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleProduction of Feline Universal Erythrocytes with Methoxy Polyethylene Glycol-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Physiology (생리학교실)-
dc.contributor.googleauthorHyung Kyu Kim-
dc.contributor.googleauthorDan Bi Ahn-
dc.contributor.googleauthorHan Byeol Jang-
dc.contributor.googleauthorJing Ma-
dc.contributor.googleauthorJuping Xing-
dc.contributor.googleauthorJoo Won Yoon-
dc.contributor.googleauthorKyung Hee Lee-
dc.contributor.googleauthorDong Min Lee-
dc.contributor.googleauthorChang Hyun Kim-
dc.contributor.googleauthorHee Young Kim-
dc.identifier.doi10.3390/jfb14090476-
dc.contributor.localIdA06338-
dc.relation.journalcodeJ04438-
dc.identifier.pmid37754890-
dc.subject.keywordRBC-
dc.subject.keywordfeline-
dc.subject.keywordmPEG-
dc.subject.keyworduniversal red blood cells-
dc.contributor.alternativeNameKim, Hee Young-
dc.contributor.affiliatedAuthor김희영-
dc.citation.volume14-
dc.citation.number9-
dc.citation.startPage476-
dc.identifier.bibliographicCitationJOURNAL OF FUNCTIONAL BIOMATERIALS, Vol.14(9) : 476, 2023-09-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Physiology (생리학교실) > 1. Journal Papers

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