branch of medicine that studies the response of organisms to  foreign substances, e.g.,
  ), and the influence of genetic, nutritional, and other factors  on the immune system. They also study disease-causing organisms  to determine how they injure the host and help to develop  vaccines (see
  ).
  In addition to studying the normal workings of the immune system,  immunologists study unwanted immune responses such as  allergiesallergy,  hypersensitive reaction of the body tissues of certain  individuals to certain substances that, in similar amounts and  circumstances, are innocuous to other persons. Allergens, or  allergy-causing substances, can be airborne substances (e.g.  ..... Click the link for more  information. , essentially immunological responses  of the body to substances or organisms that, as a rule, do not  affect most people, and autoimmune diseasesautoimmune disease,  any of a number of abnormal conditions caused when the body  produces antibodies to its own substances. In rheumatoid  arthritis, a group of antibody molecules called collectively RF,  or rheumatoid factor, is complexed to the individual's own gamma  globulin  ..... Click the link for more  information. (e.g., rheumatoid  arthritisarthritis,  painful inflammation of a joint or joints of the body, usually  producing heat and redness. There are many kinds of arthritis. In  its various forms, arthritis disables more people than any other  chronic disorder.  ..... Click the link for more  information. and lupus erythematosus) which  occur when the body reacts immunologically to some of its own  constituents.
  Immunologists have developed a large number of procedures have  been developed to detect and measure quantities of  immunologically active substances such as circulating antibodies  and immune globulinsglobulin,  any of a large family of proteins of a spherical or globular  shape that are widely distributed throughout the plant and animal  kingdoms. Many of them have been prepared in pure crystalline  form.  ..... Click the link for more  information. . Immune globulins that can be given  intravenously (IVIGs) have been found to be more effective  against antibody deficiencies and certain autoimmune diseases  than their older intramuscular counterparts; their use in a wide  spectrum of bacterial and viral infections is under study.  Current research in immunology is also aimed at understanding the  role of T lymphocytes (see immunityimmunity,  ability of an organism to resist disease by identifying and  destroying foreign substances or organisms. Although all animals  have some immune capabilities, little is known about nonmammalian  immunity.  ..... Click the link for more  information. ), which play a major part in the  body's defenses against infections and neoplasmsneoplasm  or tumor,  tissue composed of cells that grow in an abnormal way. Normal  tissue is growth-limited, i.e., cell reproduction is equal to  cell death. Feedback controls limit cell division after a certain  number of cells have developed, allowing for tissue repair  ..... Click the link for more  information. . AIDSAIDS  or acquired immunodeficiency syndrome,  fatal disease caused by a rapidly mutating retrovirus that  attacks the immune system and leaves the victim vulnerable to  infections, malignancies, and neurological disorders. It was  first recognized as a disease in 1981.  ..... Click the link for more  information. , for example, is the disease that  results when the HIVHIV,  human immunodeficiency virus, either of two closely related  retroviruses that invade T-helper lymphocytes and are responsible  for AIDS. There are two types of HIV: HIV-1 and HIV-2. HIV-1 is  responsible for the vast majority of AIDS in the United  States.  ..... Click the link for more  information. virus destroys certain of these  T cells.
  See studies by R. Desowitz (1988) and R. Gallo (1991).
  The division of biological science concerned with the native or  acquired response of complex living organisms to the intrusion of  other organisms or foreign substances. The immune system allows  the host organism to distinguish between self and nonself and to  respond to a target (termed an antigen).
  It was not until the germ theory of infectious disease was  established that the full implication of immunology was realized.  First came the recognition that certain bacteria caused  corresponding diseases. Second came the recognition that it was a  specific resistance to that bacterium or its toxins that  prevented recurrence of the same disease. Third came the  discovery that after recovery from an infectious disease,  protective substances called antibodies could be found in the  blood of animals and humans. Antigens, such as bacteria and their  products, triggered the production of antibodies and indeed all  kinds of chemical and biological molecules. The action of these  effector mechanisms, however, has come to be recognized as being  not always protective or conferring immunity, but sometimes  becoming grossly exaggerated or inappropriate, or capable of  turning upon the host in a destructive fashion that causes  disease. These responses are classified as allergies. Illnesses  associated with a misguided response of the immune system that is  directed against the self and results from a breakdown in the  normal immunological tolerance of, or unresponsiveness to, self  antigens are termed autoimmune. The mechanisms responsible for  these disorders are unknown but probably include the intervention  of factors such as viruses that either modify or naturally  resemble self molecules. Subsequently, the immune response, in  seeking out what is foreign, proceeds to attack the self.  See Allergy, Autoimmunity
  Immunology is also concerned with assaying the immune status of  the host through a variety of serological procedures, and in  devising methods of increasing host resistance through  prophylactic vaccination. There has also been much important  investigation of induced resistance and tolerance to transplants  of skin and organs, including tumors. See Blood groups, Hypersensitivity, Immunity, Immunoassay,  Isoantigen, Phagocytosis, Serology,  Transplantation biology,  Vaccination
    the science concerned with the protective reactions of the    body, or those reactions aimed at preserving the bodys    structural and functional integrity and its biological    individuality. Immunology is a broad and rapidly growing    biological discipline which started as a branch of medical    microbiology. The theoretical aspects of immunologythe study    of the cellular and molecular mechanisms governing the    formation of antibodies and their pathogenetic role and the    phylogeny and ontogeny of the immune systemare increasingly    being described by the term immunobiology.  
    Immunology originated after it was observed that individuals    who had recovered from an infectious disease were usually able    to take care of sick persons during an epidemic of that disease    without endangering themselves. In 1796, E. Jenner developed a    method for artificially immunizing human beings against    smallpox by inoculating them with cowpox. L. Pasteurs    discovery in 1880 that immunizing chickens with an old cholera    culture made them resistant to infection by the highly virulent    causative agent of fowl cholera was the beginning of immunology    as an independent science. Pasteur formulated the main    principle underlying vaccines and produced vaccines against    anthrax and rabies. In 1887, E. Metchnikoff discovered the    phenomenon of phagocytosis and developed a cellular    (phagocytic) theory of immunity. By 1890 the German    bacteriologist E. von Behring and his co-workers had shown that    protective substances, or antibodies, are formed in the body in    response to the introduction of microbes and their toxins. The    German scientist P. Ehrlich advanced the humoral theory of    immunity (1898, 1900). In 189899 the Belgian scientist J.    Bor-det and the Russian scientist N. N. Chistovich discovered    that antibodies are formed in response to the injection of    foreign erythrocytes and serum proteins. This discovery gave    rise to the study of immune responses to agents other than    infection. In 1900 the Austrian immunologist K. Landsteiner    discovered human blood groups and laid the foundation for the    theory of tissue isoantigens. A new direction in immunology    (anticipated by the Australian scientist M. Burnet), the theory    of immunological tolerance, evolved after this phenomenon was    induced experimentally by the English scientist P. Medawar in    1953.  
    Soviet immunology was initiated by the research of E.    Metchnikoff, A. A. Bezredka, G. N. Gabrichevskii, N. F.    Gamaleia, and L. A. Tarasevich. In the 1920s and 1930s Soviet    immunology not only solved practical problems but engaged in    fruitful theoretical research as well (I. L. Krichevskii, V. A.    Barykin, V. A. Liubarskii, S. I. Ginzburg-Kalinina). L. A.    Zilber, P. F. Zdrodovskii, G. V. Vygodchikov, M. P.    Pokrov-skaia, V. I. Ioffe, A. T. Kravchenko, and P. N. Kosiakov    made important contributions in the 1940s, 1950s, and 1960s.    Immunology continues to progress very rapidly, especially where    it joins with chemistry, genetics, physiology, radiobiology,    and other branches of biology and medicine. Immunology itself    consists of several more or less distinct branches (see Figure    1); these are described below.  
    Immunomorphology studies the anatomy, histology, and cytology    of the bodys immune system. It makes use of histological  
      Figure 1. Diagram of the development of ideas in      immunology and the appearance of the modern branches of the      science (after R. V. Petrov, 1968). Nobel Prizes awarded for      research in the field of immunology: (1) first, for the      theory of immunity (jointly, with P. Ehrlich, 1908); (2)      second, for the creation of antitoxic sera (1902); (3) third,      for the discovery of isoantigens and blood groups (1930); (4)      fourth, for the discovery of tolerance and a theory of      immunity (jointly, with M. Burnet, 1960). (a) First vaccine      against cholera (A. V. Khavkin, 1892).    
    and cytological methods of investigation; cultivation of cells    outside the body; light, fluorescent, and electron microscopy;    and autoradiography. In recent years the entire primary immune    response of lymphoid cells has been successfully duplicated in    a test tube. It was found that the specific immune response    and, in part, the bodys natural resistance are functions of    the lymphoid system and of phagocytic cells scattered through    all tissues. Neutrophilic and eosinophilic granulocytes,    monocytes, and thrombocytes in the blood, histiocytes in    connective tissue, microglia in the brain, cells of the sinuses    of the liver, spleen, adrenals, bone marrow, and anterior lobe    of the pituitary, reticular cells of the spleen, lymph nodes,    bone marrow, and thymus, and some circulating lymphocytes are    capable of capturing antigen. Most of the antigen introduced    into the body is captured, destroyed, and eliminated by these    cells. Only a fraction of the antigenic molecules survive long    enough to provoke specific immunological reactions. The    antigenic molecules that settle on the surface of the reticular    cells in the lymph nodes play an especially important part. The    immune response is provoked by the interaction of at least two    types of small lymphocytes that constantly migrate in the    tissues and circulate through the lymphatic and blood vessels    (see Figure 2).  
    One type of cell (the B cell) originates in bone marrow and, on    coming into contact with antigen, is converted into an    antibody-forming cell (plasma cell). Another type of cell (the    T cell) originates in the thymus. It is able to react    specifically to antigen molecules and bring about the    interaction of the B cells with antigen.  
    In an immunologically mature (immunocompetent) organism,    phagocytic cells and T and B lymphocytes carry out all forms  
      Figure 2. Diagram of the interaction of the cells of      the immune system    
    of specific response. They form circulating antibodies    belonging to various classes of the immunoglobulins (see Figure    2, upper part) and produce immune reactions of the cellular    type delayed increased sensitivity, rejection of transplant,    and so forth. The organism responds in this way to a number of    bacterial and parasitic invasions (tuberculosis, brucellosis,    leishmaniasis) and to the transplantation of cells and tissues    from another organism. The differentiation and interaction of    these cells under the influence of antigen may lead to the    development of immunological memory or of specific    immunological tolerance.  
    Comparative immunology studies the immune response in different    animal species. The evolutionary interpretation of immunity    phenomena is helpful in elucidating their mechanisms. The    lymphoid system and the ability to produce specific antibodies    appear only in vertebrates. For example, the sea lamprey has a    primitive lymphoepithelial thymus, lymphoid islets in the    spleen and bone marrow, and circulating lymphocytes. It forms    antibodies and immunological memory develops, but the set of    antigens to which the lamprey responds is very limited. The    lymphoid system is more developed in primitive cartilaginous    fish (sharks and rays), which are capable of reacting to a    great many antigens. Typical plasma cells appear in    cartilaginous, actinopterygian, and teleost fish, all of which    manufacture several types of immunoglobulins. Amphibians are    the first in the phylogenetic series to develop the system of    plasma cells, which synthesize high- and low-molecular    immunoglobulins with different antigenic properties. Reptiles    have a very similar system. The complement system (which    consists of various native serum proteins) is apparently very    ancient; it exists in a similar form both in the lower and in    the higher vertebrates.  
    In most mammals immune reactions reach full development only    after birth. A system of selective transfer of immunoglobulins    from mother to fetus functions during embryonic development,    when the embryo is protected against the effect of antigens.    However, the human fetus forms M and G immunoglobulins    independently by the fourth or fifth month. Birds and mammals,    including man, possess an identical spectrum of immunological    reactions. The degree of immunoreactivity is age-related,    decreasing noticeably as the body ages.  
    Physiology of immune reactions studies the mechanisms by which    the organism finds and removes foreign elements, or    substances that are not normal constituents of the bodys own    tissues, such as dead and malignantly degenerated cells, the    bodys own injured molecules, foreign cells and molecules,    bacteria, viruses, protozoans, and helminths and their toxins.    The functional expression of the foreignness of an antigen is    its ability to induce the formation of specific antibodies and    combine with them. The nature of antigenicity, the question of    why the organism does not form antibodies to any of the vast    number of its own molecules yet forms antibodies to an infinite    number of foreign antigens, and the essence of the specific    immune response (specifically, the synthesis of antibodies) are    the problems that constitute the main elements of the so-called    theory of antibody formation. Antibody formation, that is, the    biosynthesis of highly specialized protein molecules, is    assumed to occur like the synthesis of other blood-plasma    proteins.  
    A general theory of immunological reactions has to explain the    physicochemical nature of antigenicity, describe the molecular    mechanisms governing the synthesis of antibodies, and elucidate    the nature of immunochemical specificity. Such a theory can be    developed if three important and interrelated problems of the    immune response are successively solved: (1) the genetic basis    for the variety of immunoglobulins; (2) the number of    antibodies of different specificity that a cell can synthesize,    the nature of the intercellular interactions, and the level    (cellular or subcellular) at which antigen acts; (3) the    mechanism of specific immunological tolerance (the absence of a    specific response to antigen). The first attempt to provide a    chemical interpretation of immunological reactions was    undertaken by P. Ehrlich in 1900. He suggested that every    antibody-forming cell has a preformed side chain that by    chance corresponds spatially to an antigen. The side chains,    separated from the cell-carrier and entering the bloodstream,    were identified with antibodies. This hypothesis is strikingly    close to modern ideas of protein biosynthesis, in that it    postulates the pre-existence (preceding the action of antigen)    of a genetic code for each type of antibody. Antigen molecules    must only select the preceding structure and intensify its    reproduction. The popularity of Ehrlichs selection idea was    shaken by K. Landsteiners discovery (1936) that a great many    artificial antigens, produced synthetically, can induce the    formation of specific antibodies. Accordingly, the American    scientists F. Breinl, F. Haurowitz, D. Alexander, and S. Mudd    (1930) conjectured that preformed antibodies do not exist.    Antigen interferes with the formation of a globulin molecule by    disrupting its assembly. The result is the formation of an    antibody with a structure specific to the given antigen. The    action of the antigen in this case is described as instructive;    this readily accounts for the limitless variety of antibodies    synthesized by the organism. The American scientist L. Pauling    (1940) ascribed to antigen the role of a template where the    polypeptide chains of the antibody are formed.  
    A new stage in the development of immunology was marked by the    appearance of the concept of the Australian scientists M.    Burnet and F. Fenner (1941), who regarded antibody synthesis as    a special case of adaptive protein synthesis, similar to the    synthesis of induced enzymes in bacteria. Antigen in the cell    was assumed to have an indirect instructive function, inducing    a change in the complex of enzymes participating in the    synthesis of the antibody molecule. This concept was    subsequently supplemented by the hypothesis of the existence of    special labels for the bodys own antigens, which would    explain the natural tolerance for them. According to the    American scientist R. Owen (1957), an antigen, like a mutagen,    causes corresponding changes in deoxyribonucleic acid (DNA)    that result in the biosynthesis of antibody molecules. The    American scientist G. Goldstein (1960) suggested that antigen    acts in analogous fashion on messenger ribonucleic acid. In    1950 the German scientist N. K. Jerne advanced a new    hypothesis, based on Ehrlichs selection idea, to explain the    specific immune response. Jernes natural selection    hypothesis was essentially that antibody molecules, differing    in specificity, are formed in the thymus during the embryonic    period. The complex of antigen and corresponding antibody comes    into contact with an antibody-synthesizing cell, which uses the    antibody as a template to form similar molecules. Jerne    postulated the absence of antibodies to the bodys own antigens    and the recognition only of foreign configurations.  
    The clonal-selection theory of acquired immunity, advanced by    M. Burnet (1957), was an elaboration of the selection idea. A    clone is a group of cells descended by division from a single    precursor cell. According to Burnet, the lymphoid system of an    immunologically mature organism contains a great many (at least    104105) clones of cells capable of    responding specifically to different antigens. The nature of    the genetic diversity of the immunoglobulins is unknown.    However, the clonal-selection theory seems to be the most    plausible and consistent with modern ideas of protein    biosynthesis. Burnet ascribed the absence of a reaction to the    organisms own antigens to the elimination of any prohibited    clones (that is, clones capable of synthesizing antibodies to    ones own) during the embryonic period. According to this    theory, an antigen entering the organism selects a cell that    is capable of forming the corresponding antibody and stimulates    it to multiply and then to synthesize the antibody. Where this    selection takes placeat the level of the cell clones (as    Burnet believes) or at the level of subcellular unitsdepends    on how many antibody molecules of different specificities the    cell is capable of synthesizing. It is conceivable that the    cell bears genetic information for the synthesis of more than    105 different immunoglobulins. However, because of    differentiation, the cells ability to synthesize antibodies is    in effect neutralized. Antigen depresses the synthesis of    corresponding antibodies, so that antibodies of only a single    specificity are synthesized. This notion is the basis of the    repression-depression hypothesis advanced by the American    scientist L. Szilard, the Australian I. Finch, and the Soviet    scientists V. P. Efroimson, A. E. Gurvich, and R. S. Nezlin.  
    Immune-reactions physiology also studies the factors that    regulate the quantitative characteristics of the immune    response, including the role of the nervous system (especially    of the hypothalamus), hormones, age, nutrition, condition of    the organism (specifically, the degree of fatigue), and    external influences. It is now known that pituitary and adrenal    hormones can alter immunological reactivity and that the    placenta secretes a special hormone that to a large degree    inhibits the mothers immune reactions to the antigens of the    fetus.  
    Immunopathology studies not only extreme or injurious immune    reactions but also diseases accompanied by defects in the    immune system: hereditary and acquired agammaglobulinemias and    immunoglobulinopathies in tumors of the lymphoreticular tissue,    in nephroses, after the use of cytostatic drugs, and after    irradiation. Special attention is given to methods of    inhibiting and stimulating the immune response. Intensification    of the immune response by nonspecific stimulants (so-called    adjuvants) or by transplantation of active lymphoid tissues is    a promising approach to the treatment of infectious diseases    and defects of the immune system. Conversely, inhibition of the    immune response is a method of treating diseases with extreme    or undesirable activity of the immune system. Inhibition is    achieved by injuring lymphoid cells by irradiation, nitrogen    mustard, antimetabolites, corticosteroid hormones, and    antilymphocytic serum. The immune response can also be    suppressed by the passive introduction of antibodiesfor    example, by injecting the mothers body with antirhesus    antibodies to prevent hemolytic jaundice of the newborn.  
    The bodys reaction to the cells and macromolecules of    individuals of the same or of other species has been studied    intensively in recent years. This branch of the science is    called noninfection immunology (the study of immune responses    to agents other than infection). The proteins and cellular    membranes of every multicellular organism possess certain    unique and inimitable structural features. The differences    between individuals are due to genetic mechanisms. It is for    this reason that cells and molecules introduced into the    organism from without are recognized as foreign and evoke a    complex of immune reactions directed toward eliminating them.    Hence, despite the finest surgical technique, transplanted    organs and tissues are usually rejected, since they are unable    to overcome the barrier of tissue incompatibility. This problem    is the concern of transplantation immunology. Another branch of    noninfection immunology is the immunology of tumors, which    studies tumor antigens and the mechanisms of recognition and    elimination of malignantly degenerated cells. The scope of    noninfection immunology also includes the development of    methods for creating specific immunological tolerance; these    methods will eventually make organ transplantation a    practicable method of treating all kinds of diseases. The data    obtained by immunology are the basis for the development of    applied and clinical immunology and their various concerns,    such as immunoprophylaxis, immunotherapy, and immunodiagnosis.  
    Immunological methods of research are widely used for purposes    of precise analysis in diverse branches of medicine    (hematology, obstetrics, dermatology), and biology    (biochemistry, embryology, genetics, and anthropology).  
    There are more than 50 scientific-research institutes in the    USSR dealing with the problems of immunology. The most    important of these are the N. F. Gamaleia Institute of    Epidemiology and Microbiology of the Academy of Medical    Sciences of the USSR (the department of immunology and oncology    of this institute is an international center for the study of    tumor-specific antigens), the E. Metchnikoff Moscow Institute    of Vaccines and Sera, the L. A. Tarasevich State Control    Institute of Biomedical Preparations, the Moscow Institute of    Epidemiology and Microbiology, and the Leningrad Institute of    Experimental Medicine.  
    Among the foreign organizations doing research in immunology    are the Institute of Immunology (Basel) and the Institute of    Biochemistry of Lausanne University (Switzerland), the National    Institute of Medical Research (Mill Hill, Great Britain), the    National Cancer Institute, the National Institute of Health,    and the Rockefeller Institute of Medical Research (United    States), the Scientific Research Institute of Immunology    (Prague, Czechoslovakia), and the L. Pasteur Institute (Paris,    France). Since 1963, as part of its program on immunology, the    World Health Organization has been developing information    centers for immunology and immunoglobulins and sponsoring    symposia and conferences on immunopathology, the immunology of    parasitic diseases, the immunotherapy of cancer, the typing of    antigens of tissue incompatibility, and cellular immunity.  
    Immunological studies in the USSR are published in a number of    medical and biological journals: Zhurnal mikrobiologii,    epidemiologii i immunobiologii (since 1924),    Patologicheskaia fiziologiia i eksperimentalnaia    terapiia (since 1957), Voprosy virusologii (since    1956), Meditsinskaia parazitologiia i parazitar-nye    bolezni (since 1923), and Biulleten eksperimentalnoi    biologii i meditsiny (since 1936).  
    The following foreign journals are devoted entirely to    immunology: Journal of Immunology (Baltimore, since    1916), Journal of Experimental Medicine (New York, since    1896), Journal of Allergy (St. Louis, since 1929),    Immunology (Oxford, since 1958), Clinical and    Experimental Immunology (Oxford, since 1966),    Immunochemistry (New York, since 1964), Advances in    Immunology (New York-London, since 1961), Zeitschrift    fur Immunitats- und Allergieforschung (Jena-Stuttgart,    since 1909), International Archives of Allergy and Applied    Immunology (New York-Basel, since 1950), Revue    dImmunologie et de Therapie antimicrobienne (Paris, since    1935).  
    Many articles on immunology appear in the Russian-language    Biulleten Vsemirnoi organizatsiizdravookhraneniia    (Bulletin of the World Health Organization), in some issues of    the series of WHO technical reports, and in the international    Zhurnal gigieny, epidemiologii, mikrobiologii i    immunologii, published in Russian in Prague (since 1957).  
    Practical (including clinical) immunology is concerned with the    use of immunological reactions for the diagnosis, prevention,    and treatment of a number of diseases. It is closely related to    medical and veterinary microbiology, epidemiology, physiology    and pathophysiology, biochemistry, and endocrinology. Viral    immunology and the immunology of parasitic diseases are    independent branches of practical immunology. Immunology    studies the antigenic composition of microorganisms,    characteristics of the immune processes in various kinds of    infections, and nonspecific forms of resistance to the    causative agents of infectious diseases. Study of the    immunological processes and the immunological reconstruction of    the organism caused by noninfectious antigens of exogenous and    endogenous origin and the development of methods for    controlling allergic diseases are becoming increasingly    important. Other branches of clinical immunology are also    developing intensively. These include radiation immunology,    which studies the disruption of immunological reactivity by    irradiation, and immunohematology, which investigates the    antigenic composition of blood cells and the causes and    mechanism of development of immunological injury to the    circulatory system. Immunology is developing methods of    immunoprophylaxis, immunotherapy, and immunodiagnosis.  
    Clinical immunology uses a variety of research techniques. For    example, biochemical and physicochemical methods are used to    study the nature and properties of antigens and antibodies.    Using isotopic indicators and fluorescence microscopy,    im-munologists study the fate of antigens in the body and the    laws of antibody formation at the cellular level. The    mechanisms of development of nonspecific inflammatory and    allergic reactions are investigated by biochemical and    cytochemical methods.  
    Immunological methods of research are based on the specificity    of the interaction of an antigen (microbe, virus, foreign    protein, and so forth) with antibodies. Serology is a branch of    immunology that studies the reaction of antigen with serum    antibodies. The most widely used immunological methods include    the precipitation reaction, the agglutination reaction, lysis,    and the neutralization reaction. The interaction of antigen    with immune cells is receiving extensive study. Many    immunological methods are highly specific and sensitive (for    example, the anaphylactic reaction is more sensitive than the    methods of analytical chemistry), and they are employed in    other disciplines, such as forensic medicine.  
    Immunology is taught in the USSR and abroad in medical and    veterinary schools in departments of pathological physiology,    microbiology, and general pathology, as well as in special    scientific research institutes. Problems of clinical immunology    are discussed at international congresses on microbiology and    allergology and in many Soviet and foreign periodicals.  
      A. KH. KANCHURIN and N. V.      MEDUNITSYN    
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