Jacques Miller | |
---|---|
Born | Jacques Francis Albert Pierre Meunier 2 April 1931 Nice, France |
Citizenship | Australia |
Alma mater | The University of Sydney |
Known for | Discoveries of the function of the thymus and the T cell and B cell subsets of mammalian lymphocytes |
Awards | Gairdner Foundation International Award (1966) |
Scientific career | |
Fields | Immunology |
Institutions | The Walter and Eliza Hall Institute of Medical Research, Melbourne |
Jacques Francis Albert Pierre Miller AC FRS FAA (born 2 April 1931) is a French-Australian research scientist. He is known for having discovered the function of the thymus and for the identification, in mammalian species of the two major subsets of lymphocytes (T cells and B cells) and their function.
Miller was born on 2 April 1931 in Nice, France, as J.F.A.P. Meunier, and grew up in France, Switzerland and China, mostly in Shanghai. After the outbreak of World War II, in anticipation of Japan's entry into the war, his family moved in 1941 to Sydney, Australia, and changed their last name to "Miller". He was educated at St Aloysius' College in Sydney, where he met his future colleague, Sir Gustav Nossal. [1]
Miller studied medicine at the University of Sydney, and had his first experience of laboratory research in the laboratory of Professor Patrick de Burgh where he studied virus infection. [1]
In 1958, Miller travelled to the United Kingdom on a Gaggin Research Fellowship from the University of Queensland. He was accepted to the Chester Beatty Research Institute of Cancer Research (part of the Institute of Cancer Research, London) and as a PhD student at the University of London. [2] Miller chose to study the pathogenesis of lymphocytic leukemia in mice, expanding on the research of Ludwik Gross into murine leukemia virus. Miller showed that experimental animals without a thymus at birth were incapable of rejecting foreign tissues and resisting many infections, thus demonstrating that the thymus is vital for development and function of the adaptive immune system. Prior to this, the thymus was believed to be a vestigial organ with no function. [3] His discovery has led many to describe Miller as the "world's only living person who can claim to have been the first to have described the functions of a human organ". [4] In 1963, Miller continued his work into the function of the thymus at the National Institutes of Health.
In 1966, Miller returned to Australia to become a research group leader at the Walter and Eliza Hall Institute of Medical Research in Melbourne, at the invitation of its new director Sir Gustav Nossal, the successor of Sir Macfarlane Burnet. There, with student Graham Mitchell, he discovered that mammalian lymphocytes can be separated into what were later called T cells and B cells, and that these interact to allow normal antibody production (T cell help). Miller went on to show that the thymus produces the T cells, that it removes autoreactive T cells (central T cell tolerance) and several other landmark findings in immunology. These are considered crucial to understanding diseases such as cancer, autoimmunity and AIDS, as well as processes such as transplant rejection, allergy and antiviral immunity. [1] Miller was also the first to provide evidence that thymus-derived immune cells are important for the defense against certain tumors, [5] which forms the basis for modern cancer immunotherapy.
Semi-retired since 1996, Miller is still involved in immunological research. [4]
Miller has had a longstanding interest in art, and studied art in the 1980s. His art has been exhibited at venues in Melbourne. [6]
Immunology is a branch of biology and medicine that covers the study of immune systems in all organisms.
The thymus is a specialized primary lymphoid organ of the immune system. Within the thymus, thymus cell lymphocytes or T cells mature. T cells are critical to the adaptive immune system, where the body adapts to specific foreign invaders. The thymus is located in the upper front part of the chest, in the anterior superior mediastinum, behind the sternum, and in front of the heart. It is made up of two lobes, each consisting of a central medulla and an outer cortex, surrounded by a capsule.
T cells are one of the important types of white blood cells of the immune system and play a central role in the adaptive immune response. T cells can be distinguished from other lymphocytes by the presence of a T-cell receptor (TCR) on their cell surface.
Sir Peter Brian Medawar was a Brazilian-British biologist and writer, whose works on graft rejection and the discovery of acquired immune tolerance have been fundamental to the medical practice of tissue and organ transplants. For his scientific works, he is regarded as the "father of transplantation". He is remembered for his wit both in person and in popular writings. Richard Dawkins referred to him as "the wittiest of all scientific writers"; Stephen Jay Gould as "the cleverest man I have ever known".
Sir Frank Macfarlane Burnet, usually known as Macfarlane or Mac Burnet, was an Australian virologist known for his contributions to immunology. He won a Nobel Prize in 1960 for predicting acquired immune tolerance and he developed the theory of clonal selection.
Graft-versus-host disease (GvHD) is a syndrome, characterized by inflammation in different organs. GvHD is commonly associated with bone marrow transplants and stem cell transplants.
WEHI, previously known as the Walter and Eliza Hall Institute of Medical Research, and as the Walter and Eliza Hall Institute, is Australia's oldest medical research institute. Sir Frank Macfarlane Burnet, who won the Nobel Prize in 1960 for his work in immunology, was director from 1944 to 1965. Burnet developed the ideas of clonal selection and acquired immune tolerance. Later, Professor Donald Metcalf discovered and characterised colony-stimulating factors. As of 2015, the institute hosted more than 750 researchers who work to understand, prevent and treat diseases including blood, breast and ovarian cancers; inflammatory diseases (autoimmunity) such as rheumatoid arthritis, type 1 diabetes and coeliac disease; and infectious diseases such as malaria, HIV and hepatitis B and C.
In immunology, clonal selection theory explains the functions of cells of the immune system (lymphocytes) in response to specific antigens invading the body. The concept was introduced by Australian doctor Frank Macfarlane Burnet in 1957, in an attempt to explain the great diversity of antibodies formed during initiation of the immune response. The theory has become the widely accepted model for how the human immune system responds to infection and how certain types of B and T lymphocytes are selected for destruction of specific antigens.
In immunology, central tolerance is the process of eliminating any developing T or B lymphocytes that are autoreactive, i.e. reactive to the body itself. Through elimination of autoreactive lymphocytes, tolerance ensures that the immune system does not attack self peptides. Lymphocyte maturation occurs in primary lymphoid organs such as the bone marrow and the thymus. In mammals, B cells mature in the bone marrow and T cells mature in the thymus.
X-linked severe combined immunodeficiency (X-SCID) is an immunodeficiency disorder in which the body produces very few T cells and NK cells.
Immune tolerance, or immunological tolerance, or immunotolerance, is a state of unresponsiveness of the immune system to substances or tissue that would otherwise have the capacity to elicit an immune response in a given organism. It is induced by prior exposure to that specific antigen and contrasts with conventional immune-mediated elimination of foreign antigens. Tolerance is classified into central tolerance or peripheral tolerance depending on where the state is originally induced—in the thymus and bone marrow (central) or in other tissues and lymph nodes (peripheral). The mechanisms by which these forms of tolerance are established are distinct, but the resulting effect is similar.
Rupert Everett Billingham FRS was a British biologist who did significant research in the fields of reproductive immunology and organ transplantation. "He made numerous fundamental contributions to our modern knowledge of the mechanisms of graft rejection and how to prevent it, and he analysed some of the mechanisms responsible for the survival of the mammalian foetus in an immunologically hostile environment".
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.
Human leukocyte antigens (HLA) began as a list of antigens identified as a result of transplant rejection. The antigens were initially identified by categorizing and performing massive statistical analyses on interactions between blood types. This process is based upon the principle of serotypes. HLA are not typical antigens, like those found on surface of infectious agents. HLAs are alloantigens, they vary from individual to individual as a result of genetic differences. An organ called the thymus is responsible for ensuring that any T-cells that attack self proteins are not allowed to live. In essence, every individual's immune system is tuned to the specific set of HLA and self proteins produced by that individual; where this goes awry is when tissues are transferred to another person. Since individuals almost always have different "banks" of HLAs, the immune system of the recipient recognizes the transplanted tissue as non-self and destroys the foreign tissue, leading to transplant rejection. It was through the realization of this that HLAs were discovered.
Thymic involution is the shrinking (involution) of the thymus with age, resulting in changes in the architecture of the thymus and a decrease in tissue mass. Thymus involution is one of the major characteristics of vertebrate immunology, and occurs in almost all vertebrates, from birds, teleosts, amphibians to reptiles, though the thymi of a few species of sharks are known not to involute. This process is genetically regulated, with the nucleic material responsible being an example of a conserved sequence — one maintained through natural selection since it arose in a common ancestor of all species now exhibiting it, via a phenomenon known to bioinformaticists as an orthologic sequence homology.
Max Dale Cooper, is an American immunologist and a professor at the Department of Pathology and Laboratory Medicine and the Emory Vaccine Center of Emory University School of Medicine. He is known for characterizing T cells and B cells.
Gabrielle T. Belz is an Australian molecular immunologist and viral immunologist. She is a faculty member of the Walter and Eliza Hall Institute of Medical Research, within the Molecular Immunology division. Belz has made important contributions to the understanding of immune system function, especially in relation to the molecular and cellular signalling pathways of immune response to viruses. Her research has focused on understanding the signals that drive the initial development of protective immunity against pathogen infections, such as influenza and herpes viruses. This includes research into how cytotoxic T cells recognise and remove virally-infected cells from the body following infection. Research into the description of the specific factors and response during infection will contribute towards the long-term development of vaccines for infectious disease, and the development of better treatments for autoimmune diseases.
Ray David Owen was a teacher and scientist whose discovery of unusual, “mixed,” red blood cell types in cattle twins in 1945 launched the fields of modern immunology and organ transplantation. Owen's 1945 findings were published in the journal Science. This observation demonstrated that self was “learned” by the immune system during development and paved the way for research involving induction of immune tolerance and early tissue grafting. When Frank Macfarlane Burnet and Sir Peter Brian Medawar were awarded their 1960 Nobel Prize in Physiology or Medicine for the discovery of acquired immunological tolerance, Owen was not mentioned in the prize. However, in a letter to Owen, Medawar stated that he believed Owen should have also been included in the prize. Owen also led the successful effort to admit women as California Institute of Technology undergraduates.
Immunology & Cell Biology is an academic journal of the Australian and New Zealand Society for Immunology covering basic immunology research. The journal has a focus on cellular immunology, innate and adaptive immunity, immune responses to pathogens, tumour immunology, immunopathology, immunotherapy, immunogenetics and immunological studies in humans and model organisms. The journal was founded in 1924 as the Australian Journal of Experimental Biology and Medical Science, and was converted in 1987 to Immunology and Cell Biology, making it one of the oldest speciality immunology journals in existence. Major historical contributions including publication by Donald Metcalf of the strategy for identifying colony-stimulating factors (CSFs) and the development of the clonal selection theory by Frank Macfarlane Burnet, in a series of more than 90 publications in the 1970s.
Infectious tolerance is a term referring to a phenomenon where a tolerance-inducing state is transferred from one cell population to another. It can be induced in many ways; although it is often artificially induced, it is a natural in vivo process. A number of research deal with the development of a strategy utilizing this phenomenon in transplantation immunology. The goal is to achieve long-term tolerance of the transplant through short-term therapy.
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