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ABO blood group antigens and differential glycan expression: Perspective on the evolution of common human enzyme deficiencies.

作者信息

Jajosky Ryan Philip, Wu Shang-Chuen, Zheng Leon, Jajosky Audrey N, Jajosky Philip G, Josephson Cassandra D, Hollenhorst Marie A, Sackstein Robert, Cummings Richard D, Arthur Connie M, Stowell Sean R

机构信息

Joint Program in Transfusion Medicine, Brigham and Women's Hospital, Harvard Medical School, 630E New Research Building, 77 Avenue Louis Pasteur, Boston, MA 02115, USA.

Biconcavity Inc, Lilburn, GA, USA.

出版信息

iScience. 2022 Dec 14;26(1):105798. doi: 10.1016/j.isci.2022.105798. eCollection 2023 Jan 20.


DOI:10.1016/j.isci.2022.105798
PMID:36691627
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9860303/
Abstract

Enzymes catalyze biochemical reactions and play critical roles in human health and disease. Enzyme variants and deficiencies can lead to variable expression of glycans, which can affect physiology, influence predilection for disease, and/or directly contribute to disease pathogenesis. Although certain well-characterized enzyme deficiencies result in overt disease, some of the most common enzyme deficiencies in humans form the basis of blood groups. These carbohydrate blood groups impact fundamental areas of clinical medicine, including the risk of infection and severity of infectious disease, bleeding risk, transfusion medicine, and tissue/organ transplantation. In this review, we examine the enzymes responsible for carbohydrate-based blood group antigen biosynthesis and their expression within the human population. We also consider the evolutionary selective pressures, e.g. malaria, that may account for the variation in carbohydrate structures and the implications of this biology for human disease.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c945/9860303/f0efbe0c4615/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c945/9860303/b5b1b235a906/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c945/9860303/cebde8f90062/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c945/9860303/9537840bddc4/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c945/9860303/f0efbe0c4615/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c945/9860303/b5b1b235a906/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c945/9860303/cebde8f90062/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c945/9860303/9537840bddc4/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c945/9860303/f0efbe0c4615/gr3.jpg

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[3]
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本文引用的文献

[1]
Comprehensive analysis of platelet glycoprotein Ibα ectodomain glycosylation.

J Thromb Haemost. 2023-4

[2]
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants.

Nat Genet. 2022-12

[3]
The Development and Consequences of Red Blood Cell Alloimmunization.

Annu Rev Pathol. 2023-1-24

[4]
A virtuosic CADENZA played by sutimlimab.

Blood. 2022-9-1

[5]
An Automated Approach to Assess Relative Galectin-Glycan Affinity Following Glycan Microarray Analysis.

Front Mol Biosci. 2022-8-11

[6]
A first update on mapping the human genetic architecture of COVID-19.

Nature. 2022-8

[7]
Caspase Activation and Inhibition.

Cold Spring Harb Perspect Biol. 2022-8-1

[8]
Nucleocapsid Antigenemia Is a Marker of Acute SARS-CoV-2 Infection.

J Infect Dis. 2022-11-1

[9]
The respective relevance of sensitization to alloantigens and xenoantigens in pig organ xenotransplantation.

Hum Immunol. 2023-1

[10]
Innate immune Galectin-7 specifically targets microbes that decorate themselves in blood group-like antigens.

iScience. 2022-5-30

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