高雄市生物科技發展協會|http://www.khba.org.tw
會員登入
記住帳號 自動登入
會員名錄
各式辦法
下載專區
留言板
您目前的位置:首頁 / 活動與新訊
Enzyme discovery paves the way for developing universal donor blood
活動日期:2024.06.05
2024.06.05  

Enzyme discovery paves the way for developing universal donor blood

https://www.news-medical.net/news/20240429/Enzyme-discovery-paves-the-way-for-developing-universal-donor-blood.aspx?utm_source=azonetwork_newsletter&utm_medium=email&utm_campaign=biochemistry_newsletter_21_may_2024

Apr 29 2024DTU (Technical University of Denmark)

Researchers at DTU and Lund University have discovered enzymes that remove hindrances that stood in the way of developing universal donor blood.

The quest to develop universal donor blood has taken a decisive step forward. Researchers at DTU and Lund University have discovered enzymes that, when mixed with red blood cells, are able to remove specific sugars that make up the A and B antigens in the human ABO blood groups. The results have been published in the scientific journal Nature Microbiology: https://www.nature.com/articles/s41564-024-01663-4

"For the first time, the new enzyme cocktails not only remove the well-described A and B antigens, but also extended variants previously not recognized as problematic for transfusion safety. We are close to being able to produce universal blood from group B donors, while there is still work to be done to convert the more complex group A blood. Our focus is now to investigate in detail if there are additional obstacles and how we can improve our enzymes to reach the ultimate goal of universal blood production," says Professor Maher Abou Hachem, who is the study leader at DTU and one of the senior scientists behind the discovery.

He states that the discovery is the result of combining the expertise of DTU researchers in enzymes from the human gut microbiota and Lund University researchers in carbohydrate-based blood groups and transfusion medicine.

High demand for donor blood

Human red blood cells carry specific complex sugars structures (antigens) that define the four ABO blood groups A, B, AB and O. These antigens control compatibility between donors and recipients for safe blood transfusion and organ transplantation. Donor blood is screened for disease markers and the main blood groups. It can then be stored refrigerated for up to 42 days.

The need for donor blood is high due to the elderly making up a larger proportion of the population and more patients undergoing blood-intensive medical procedures. Successfully converting A or B blood types into ABO universal donor blood can markedly reduce the logistics and costs currently associated with storing four different blood types. In addition, the development of universal donor blood will lead to an increased supply of donor blood by reducing the waste of blood approaching its expiry date.

The reason why it is necessary to remove the A and B antigens to create universal donor blood is because they can trigger life-threatening immune reactions when transfused into non-matched recipients.

The concept of using enzymes to generate universal donor blood was introduced more than 40 years ago. Since then, higher efficiency enzymes to remove the A and B antigens were discovered, but researchers are still not able to explain or abolish all immune reactions related to the blood, and therefore these enzymes are still not used in clinical practice.

Enzymes from the gut

The research groups from DTU and Lund University have gone new ways to find enzymes that can remove both the A and B blood antigens and the sugars that block them. The research teams discovered new mixtures of enzymes from the human gut bacterium Akkermansia muciniphila that feeds by breaking down the mucus, which covers the surface of the gut. It turns out that these enzymes are exceptionally efficient, as the complex sugars at the surface of the intestinal mucosa share chemical resemblance with those found at the surface of blood cells.

What is special about the mucosa is that bacteria, which are able to live on this material, often have tailor-made enzymes to break down mucosal sugar structures, which include blood group ABO antigens. This hypothesis turned out to be correct."

Professor Maher Abou Hachem, study leader at DTU

Pittcon Highlights: Bioanalytical and Life Sciences eBook Check out the highlights from Pittcon in the Bioanalytical & Life Sciences IndustryDownload the latest edition

The researchers in this study tested 24 enzymes, which they used to process hundreds of blood samples.

"Universal blood will create a more efficient utilization of donor blood, and also avoid giving ABO-mismatched transfusions by mistake, which can otherwise lead to potentially fatal consequences in the recipient. When we can create ABO-universal donor blood, we will simplify the logistics of transporting and administering safe blood products, while at the same time minimizing blood waste" says Professor Martin L. Olsson, the leader of the study at Lund University.

The researchers from DTU and Lund University have applied for a patent on the new enzymes and the method for enzyme treatment and expect to make further progress on this in their new joint project over the next three and a half years. If successful, the concept needs to be tested in controlled patient trials before this can be considered for commercial production and clinical use.

The initial research project is funded by the Independent Research Fund Denmark (Technology and Production Sciences, FTP), the Swedish Research Council, ALF grants from the Swedish government and county councils as well as the Knut and Alice Wallenberg Foundation and Research Fund Denmark, Natural Sciences, FNU), while the new continued project is funded by the Novo Nordisk Foundation, Interdisciplinary Synergy Programme.

Source:

DTU (Technical University of Denmark)

Journal reference:

Jensen, M., et al. (2024). Akkermansia muciniphila exoglycosidases target extended blood group antigens to generate ABO-universal blood. Nature Microbiologydoi.org/10.1038/s41564-024-01663-4.

 

共有314筆資料 頁數: 第4頁(共16頁)
編號 標題 新增日期
1 Journey to the Center of the Ear 2023.09.13
2 A Bacterial Culprit for Rheumatoid Arthritis 2023.09.05
3 Pet Hamsters Spread SARS-CoV-2 in Hong Kong: Preprint 2022.02.08
4 What We Learned About COVID-19 in 2021 2022.01.11
5 獨家》國衛院新研究:阿茲海默症乙型類澱粉蛋白會加速新冠病毒.. 2021.11.29
6 《Science》憂鬱症關鍵腦部受體GPR158結構終破解! 可望成治療.. 2021.11.25
7 國衛院領先全球》全身性紅斑狼瘡 致病源頭找到了 2021.11.09
8 Spiny Mice Appear to Regenerate Damaged Kidneys 2021.11.05
9 健康網》喜好口味一直變? 研究:味覺隨年紀增加而下降 2021.10.29
10 Delta後代傳播力更強! 英示警:亞系變異株「AY.4.2」崛起 2021.10.27
11 Red Blood Cells Activate Innate Immune System 2021.10.22
12 Mice that Survive Infection Pass on Stronger Immunit 2021.10.20
13 How Commensal Gut Bacteria Keep Pathogens in Check 2021.10.15
14 Repurposed Drug Reverses Signs of Alzheimer’s in Mice, Hu.. 2021.10.13
15 獨家》糖尿病可治癒!中研院團隊新發現有機會取代胰島素 2021.09.24
16 SARS-CoV-2’s Wide-Ranging Effects on the Body 2021.09.22
17 A Surge in Pandemic Research Shines a Spotlight on Preprints 2021.09.17
18 去年國人10大死因出爐 癌症、心臟病、肺炎仍居前三名 2021.06.18
19 中藥治武肺 清冠一號獲核准 2021.05.19
20 Brain’s Lymphatic System Tied to Alzheimer’s Symptoms in.. 2021.05.10
上一頁  1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16  下一頁
版權所有©2006 高雄市生物科技發展協會 所有文字、資料禁止轉用
地址:高雄市中正一路120號14樓之3 TEL:(07)591-9569 / FAX:(07)591-9018 / e-mail: khba.tw@gmail.com
累積進站人數:3123240