MRC Blood Group Unit

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The MRC Blood Group Unit, originally the Blood Group Research Unit, was a research unit of the British Medical Research Council from 1946 to 1995. Initially established in the Lister Institute, it transferred to the Galton Laboratory (the Genetics department) of University College, London in 1975, the original home of its predecessor. [1]

Contents

The unit mainly used serological techniques to discover blood group antigens. Only in the last 15 years of its existence were monoclonal antibodies and molecular approaches adopted. Blood groups were used to study many aspects of human genetics: including those related to blood transfusion, linkage analysis, mosaicism and chimaerism.

Directors

Scientific achievements

These are listed roughly in chronological order of the start of the research. Research on most topics was on-going with significant publications spanning several decades: for instance Xg was discovered in the early 1960s, [2] but the unit contributed to the identification of the underlying gene, PBDX, in 1994. [3]

Related Research Articles

<span class="mw-page-title-main">Blood type</span> Classification of blood based on antibodies and antigens on red blood cell surfaces

A blood type is a classification of blood, based on the presence and absence of antibodies and inherited antigenic substances on the surface of red blood cells (RBCs). These antigens may be proteins, carbohydrates, glycoproteins, or glycolipids, depending on the blood group system. Some of these antigens are also present on the surface of other types of cells of various tissues. Several of these red blood cell surface antigens can stem from one allele and collectively form a blood group system.

<span class="mw-page-title-main">ABO blood group system</span> Classification of blood types

The ABO blood group system is used to denote the presence of one, both, or neither of the A and B antigens on erythrocytes. For human blood transfusions, it is the most important of the 44 different blood type classification systems currently recognized by the International Society of Blood Transfusions (ISBT) as of December 2022. A mismatch in this serotype can cause a potentially fatal adverse reaction after a transfusion, or an unwanted immune response to an organ transplant. Such mismatches are rare in modern medicine. The associated anti-A and anti-B antibodies are usually IgM antibodies, produced in the first years of life by sensitization to environmental substances such as food, bacteria, and viruses.

<span class="mw-page-title-main">Jean Dausset</span> French immunologist (1916–2009)

Jean-Baptiste-Gabriel-Joachim Dausset was a French immunologist born in Toulouse, France. Dausset received the Nobel Prize in Physiology or Medicine in 1980 along with Baruj Benacerraf and George Davis Snell for their discovery and characterisation of the genes making the major histocompatibility complex. Using the money from his Nobel Prize and a grant from the French Television, Dausset founded the Human Polymorphism Study Center (CEPH) in 1984, which was later renamed the Foundation Jean Dausset-CEPH in his honour. He married Rose Mayoral in 1963, with whom he had two children, Henri and Irène. Jean Dausset died on June 6, 2009, in Majorca, Spain, at the age of 92.

<span class="mw-page-title-main">Alexander S. Wiener</span> American geneticist

Alexander Solomon Wiener, was an American biologist and physician, specializing in the fields of forensic medicine, serology, and immunogenetics. His work led to the discovery of the Rh factor in 1937, along with Karl Landsteiner, and subsequently to the development of exchange transfusion methods that saved the lives of infants with hemolytic disease of the newborn. He received a Lasker Award for his achievement in 1946.

The term human blood group systems is defined by the International Society of Blood Transfusion (ISBT) as systems in the human species where cell-surface antigens—in particular, those on blood cells—are "controlled at a single gene locus or by two or more very closely linked homologous genes with little or no observable recombination between them", and include the common ABO and Rh (Rhesus) antigen systems, as well as many others; 44 human systems are identified as of 31 December 2022.

The Kell antigen system is a human blood group system, that is, a group of antigens on the human red blood cell surface which are important determinants of blood type and are targets for autoimmune or alloimmune diseases which destroy red blood cells. The Kell antigens are K, k, Kpa, Kpb, Jsa and Jsb. The Kell antigens are peptides found within the Kell protein, a 93-kilodalton transmembrane zinc-dependent endopeptidase which is responsible for cleaving endothelin-3.

<span class="mw-page-title-main">Rh blood group system</span> Human blood group system involving 49 blood antigens

The Rh blood group system is a human blood group system. It contains proteins on the surface of red blood cells. After the ABO blood group system, it is the most likely to be involved in transfusion reactions. The Rh blood group system consisted of 49 defined blood group antigens in 2005. As of 2023, there are over 50 antigens among which the five antigens D, C, c, E, and e are the most important. There is no d antigen. Rh(D) status of an individual is normally described with a positive (+) or negative (−) suffix after the ABO type. The terms Rh factor, Rh positive, and Rh negative refer to the Rh(D) antigen only. Antibodies to Rh antigens can be involved in hemolytic transfusion reactions and antibodies to the Rh(D) and Rh antigens confer significant risk of hemolytic disease of the newborn.

<span class="mw-page-title-main">Arthur Mourant</span> British Genetic anthropologist

Arthur Ernest Mourant FRS was a British chemist, hematologist and geneticist who pioneered research into biological anthropology and its distribution, genetics, clinical and laboratory medicine, and geology.

<i>RHCE</i> (gene) Protein-coding gene in the species Homo sapiens

Blood group Rh(CE) polypeptide is a protein that in humans is encoded by the RHCE gene. RHCE has also recently been designated CD240CE.

The Sir William Dunn School of Pathology is a department within the University of Oxford. Its research programme includes the cellular and molecular biology of pathogens, the immune response, cancer and cardiovascular disease. It teaches undergraduate and graduate courses in the medical sciences.

<span class="mw-page-title-main">Xg antigen system</span> Blood group system

The XG antigen is a red blood cell surface antigen discovered in 1962. by researchers at the MRC Blood Group Unit.

<span class="mw-page-title-main">Robert Russell Race</span>

Robert Russell Race was a British medical doctor and human geneticist. He was Director of the Medical Research Council Blood Group Unit, of the Lister Institute of Preventive Medicine. His second wife, whom he married in 1956, was Ruth Sanger, who succeeded him in the post.

<span class="mw-page-title-main">Ruth Sanger</span> Australian haematologist

Ruth Ann Sanger was an Australian immunogeneticist, haematologist and serologist. She was known for her work on human red cell antigens and for the genetic mapping of the human X chromosome. She was Director of the Medical Research Council Blood Group Unit, of the Lister Institute of Preventive Medicine from 1973 to 1983.

Sylvia Dorothy Lawler was an English geneticist who worked in the field of human genetics.

Karen Penelope Steel FRS FMedSci is a British scientist who studies the genetics of deafness, using the mouse as a model to identify the genes involved and to understand the molecular, cellular and physiological mechanisms involved. She is Professor of Sensory Function at the Wolfson Centre for Age-Related Diseases, King's College London. Previously she was Principal Investigator of the Genetics of Deafness research programme at the Wellcome Trust Sanger Institute.

<span class="mw-page-title-main">Ketan J. Patel</span>

Ketan Jayakrishna Patel is a British–Kenyan scientist who is Director of the MRC Weatherall Institute of Molecular Medicine and the MRC Molecular Haematology Unit at the University of Oxford. Until 2020 he was a tenured principal investigator at the Medical Research Council (MRC) Laboratory of Molecular Biology (LMB).

<span class="mw-page-title-main">Sue Povey</span> British geneticist (1942–2019)

Professor Susan Povey FMedSci, was a British geneticist.

<span class="mw-page-title-main">Patrick Mollison</span> British haematologist

Patrick Loudon Mollison,, was a British haematologist, described as 'the father of transfusion medicine'.

<span class="mw-page-title-main">Willy A. Flegel</span> German-American medical researcher

Willy Albert Flegel is a German-American medical researcher, geneticist, and physician who is best known for his work in the field of the Rh blood group. Flegel is the chief of the laboratory services section of the Department of Transfusion Medicine at the National Institutes of Health Clinical Center (NIH). He lives in Washington D.C. and Frankfurt am Main, Germany.

<span class="mw-page-title-main">Weatherall Institute of Molecular Medicine</span> British medical research institute

The MRC Weatherall Institute of Molecular Medicine at the University of Oxford is a research institute located at the John Radcliffe Hospital in Oxford. Founded in 1989 by Sir David Weatherall, the institute focuses on furthering our understanding of clinical medicine at a molecular level. It was one of the first institutes of its kind in the world to be dedicated to research in this area.

References

  1. Peter S. Harper (24 September 2008). A Short History of Medical Genetics. Oxford University Press, USA. pp. 331–. ISBN   978-0-19-020839-4.
  2. Mann JJ, Cahan A, Gelb AG, et al. A sex-linked blood group. Lancet. 1962;i:8.
  3. Ellis NA, Tippett P, Petty A, et al. (November 1994). "PBDX is the XG blood group gene". Nat. Genet. 8 (3): 285–90. doi:10.1038/ng1194-285. PMID   7533029.
  4. Mazumdar, Pauline M. H. (1995). Species and Specificity: An Interpretation of the History of Immunology. Cambridge University Press. p. 347. ISBN   978-0-521-52523-7.