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    Home»Biology»Bloodlines Redefined: The Discovery of the MAL Blood Group System
    Biology

    Bloodlines Redefined: The Discovery of the MAL Blood Group System

    By University of BristolSeptember 20, 2024No Comments7 Mins Read
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    Recent studies have unveiled the MAL blood group system, identifying the Mal protein as key to the AnWj antigen expression. This advances the safety of blood transfusions by facilitating precise identification of AnWj-negative patients, potentially reducing life-threatening complications.

    Groundbreaking research has established a new blood group system, the MAL, now recognized as the 47th type.

    The discovery of a new blood group, MAL, has solved a 50- year-old mystery. Researchers from NHS Blood and Transplant (Bristol), NHSBT’s International Blood Group Reference Laboratory (IBGRL) and the University of Bristol identified the genetic background of the previously known but mysterious AnWj blood group antigen. The findings allow the identification and treatment of rare patients lacking this blood group.

    AnWj-Negative Blood Group Phenotype

    Some people can lack this blood group due to the effect of illness, but the rare inherited form of the AnWj-negative phenotype has only been found in a handful of individuals – though due to this discovery it will now be easier to find others in the future.

    The two best-known blood group systems are ABO and Rh but blood is more complex and matching across the other groups can be lifesaving.

    Impact of AnWj-Negative Phenotype on Transfusions

    If people who are AnWj-negative receive AnWj-positive blood they could have a transfusion reaction, and this research allows development of new genotyping tests for detecting such rare individuals and reducing the risk of transfusion-associated complications.

    The AnWj antigen – an antigen is a surface marker – was discovered in 1972 but its genetic background was unknown until now.[4] The new research, published by Blood, the journal of the American Society of Hematology, and now available online in pre-print, establishes a new blood group system (MAL), the 47th ever to be discovered, as home to the AnWj antigen.

    Genetic Analysis of AnWj-Negative Individuals

    The research team established that AnWj is carried on the Mal protein. More than 99.9% of people are AnWj-positive, and such individuals were shown to express full-length Mal protein on their red cells, which was not present on the cells of AnWj-negative individuals. The team identified homozygous deletions in the MAL gene associated with the inherited AnWj-negative phenotype.

    The most common reason for being AnWj-negative is due to suffering from a hematological disorder or some types of cancer that suppress antigen expression.[5] Only a very small number of people are AnWj-negative due to a genetic cause. There were five genetically AnWj negative individuals in the study including a family of Arab-Israelis.[6] The blood tested included a sample given by a lady in 2015 who was the first AnWj negative person to be discovered in the 1970s.

    Advancements in Genetic Sequencing for Blood Typing

    The research team used whole exome sequencing – the genetic sequencing of all DNA that encodes proteins – to show that these rare inherited cases were caused by homozygous DNA sequence deletions in the MAL gene, which codes for Mal protein.

    Proof that Mal is responsible for binding of AnWj antibodies isolated from these rare patients was provided by experiments showing the appearance of specific reactivity with cells in which researchers introduced the normal MAL gene but not the mutant gene.

    Significance of the Research

    Louise Tilley, Senior Research Scientist, IBGRL Red Cell Reference at NHS Blood and Transplant, said: “The genetic background of AnWj has been a mystery for more than 50 years, and one which I personally have been trying to resolve for almost 20 years of my career. It represents a huge achievement, and the culmination of a long team effort, to finally establish this new blood group system and be able to offer the best care to rare, but important, patients.

    “The work was difficult because the genetic cases are very rare. We would not have achieved this without exome sequencing, as the gene we identified wasn’t an obvious candidate and little is known about Mal protein in red cells. Proving our findings was challenging, and we appreciate the help of all our collaborators, and the patients, without whom we would not have got to this point.”

    Future Implications and Benefits

    Ash Toye, Professor of Cell Biology in the School of Biochemistry and Director of the NIHR Blood and Transplant Research Unit in red cell products at the University of Bristol, said: “It’s really exciting we were able use our ability to manipulate gene expression in the developing blood cells to help confirm the identity of the AnWj blood group, which has been an outstanding puzzle for half a century. This development will help identify these rare donors and help patients in the future.”

    Nicole Thornton, Head of IBGRL Red Cell Reference at NHS Blood and Transplant, said: “Resolving the genetic basis for AnWj has been one of our most challenging projects. 

    “There is so much work that goes into proving that a gene does actually encode a blood group antigen, but it is what we are passionate about, making these discoveries for the benefit of rare patients around the world.

    “Now genotyping tests can be designed to identify genetically AnWj-negative patients and donors. Such tests can be added to the existing genotyping platforms.”

    Dr. Tim Satchwell, Senior Lecturer at UWE Bristol, who contributed to the study while a Research Fellow at the University of Bristol, said: “Mal is a very small protein with some interesting properties which made it difficult to identify and meant we needed to pursue multiple lines of investigation to accumulate the proof we needed to establish this blood group system. Being able to combine our expertise to finally achieve this has brought the whole team a lot of satisfaction.”

    Reference: “Deletions in the MAL gene result in loss of Mal protein, defining the rare inherited AnWj-negative blood group phenotype” by Louise A Tilley, Vanja Karamatic Crew, Tosti J Mankelow, Samah A AlSubhi, Benjamin Jones, Abigail Borowski, Vered Yahalom, Lilach Finkel, Belinda K Singleton, Piers J Walser, Ashley Mark Toye, Timothy J Satchwell, Nicole M Thornton, 18 August 2024, Blood.
    DOI: 10.1182/blood.2024025099

    Further Information

    1. Donate blood and find out your ABO and rhesus blood types via www.blood.co.uk.
    2. The research was led by NHS Blood and Transplant led the work, through its International Blood Group Reference Laboratory in Bristol. Research partners included the School of Biochemistry at the University of Bristol, the Apheresis Institute at Rabin Medical Centre in Israel, Magen David Adom National Blood Services in Israel, the NIHR Blood and Transplant Research Unit in Genomics to Enhance Microbiology Screening, the Clinical Biotechnology Centre at NHS Blood and Transplant, and the National Institute for Health Research (NIHR) Blood and Transplant Research Unit in Red Blood Cell Products.
    3. Blood groups are complex. The two best-known blood group systems are ABO and Rh. Within each blood group, red cells can carry surface markers called antigens. For example, within the ABO blood group system, there are the A and B antigens – people with A have the A antigen, people with B have the B antigen, people with AB blood have both, and people with O have neither. There are now 47 recognized blood group systems together containing more than 360 recognized blood antigens.
    4. AnWj is named after the first people who made the antibody (Anton and Wj).
    5. The disorders suppress Mal and make patients AnWj-negative, unless they have the rare inherited form (MAL deletion). The inherited AnWj-negative people are healthy.
    6. The first family discovered with the inherited form is Arab-Israeli and there are other cases from this region. However, the ethnicity of all cases is not known and it is not yet known if the blood type is more common in any ethnicity.

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