Evidence map›Paper›PMID 37754890›Full record

ArticleJournal of functional biomaterials2023

Production of Feline Universal Erythrocytes with Methoxy Polyethylene Glycol.

Hyung Kyu Kim, Dan Bi Ahn, Han Byeol Jang, Jing Ma, Juping Xing, Joo Won Yoon, Kyung Hee Lee, Dong Min Lee, Chang Hyun Kim, Hee Young Kim

Open access · goldAbstract read
In one paragraph

Article in Journal of functional biomaterials, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 35% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Hyung Kyu KimDepartment of Physiology, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Dan Bi AhnDepartment of Physiology, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Han Byeol JangDepartment of Physiology, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Jing MaDepartment of Physiology, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Juping XingDepartment of Physiology, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Joo Won YoonDepartment of Physiology, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Kyung Hee LeeKABB, Daegu 42212, Republic of Korea.
Dong Min LeeKABB, Daegu 42212, Republic of Korea.
Chang Hyun KimKABB, Daegu 42212, Republic of Korea.
Hee Young KimDepartment of Physiology, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Yonsei University · KR

Funding

Korea Institute of Planning and Evaluation for Technology in Food, Agriculture and Forestry(IPET) under the Companion Animal Life Cycle Industry Technology Development Program, funded by the Ministry of Agriculture, Food and Rural Affairs(MAFRA) 322096-5
6 · The paper itself

Abstract

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.

Indexed as

felinemPEGRBCuniversal red blood cells

Identifiers

PMID37754890
PMCPMC10532140
OpenAlexW4386837346

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.