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Untitled - D Ank Unlimited

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Rood, J. J. van 629 Rose–Waaler test<br />

produced a definite reaction was defined as the minimal<br />

reaction dose (MRD). In general, the MRD of a toxin is<br />

equivalent to about 1/250 to 1/500 of the MLD (minimal<br />

lethal dose). The Lr is the smallest amount of toxin that,<br />

after mixing with one unit of antitoxin, will produce a<br />

minimal skin lesion when injected intracutaneously into a<br />

guinea pig.<br />

J.J. van Rood.<br />

Rood, J. J. van<br />

Researcher in The Netherlands who wrote his doctoral<br />

thesis on leukocyte grouping and techniques. He reported<br />

the first two allele systems. He named them 4a and 4b. They<br />

were difficult to define because they were “public antigens”<br />

shared by many molecules. By testing leukocyte alloantibodies<br />

obtained from the sera of a large number of pregnant<br />

women against leukocytes from 100 unrelated donors, he<br />

developed a systematic approach to decipher the complexity<br />

of the HLA system. van Rood and associates described nine<br />

HLA antigens and a diallelic system not linked to HLA<br />

(the Group Five system). Balner and van Rood showed that<br />

leukocyte antigens were transplantation antigens. van Rood<br />

made many contributions to HLA research.<br />

roquinimex<br />

An immunomodulating drug capable of augmenting natural<br />

killer (NK) cell numbers and reactivity and stimulating<br />

various T and B cell functions. It has been used to stimulate<br />

immune function in patients after bone marrow transplants.<br />

By contrast, it prevents relapses of chronic relapsing allergic<br />

encephalomyelitis in animal models of that disease. It also<br />

reduces relapses, disease activity, and disease progression<br />

in multiple sclerosis patients. If confirmed in further studies,<br />

this immunomodulator will have a significant future<br />

role in clinical medicine.<br />

Rose, Noel Richard (1927–)<br />

American immunologist and authority on autoimmune<br />

disease. Rose and Witebsky discovered experimental autoimmune<br />

thyroiditis. Rose’s discovery in the mid-1950s that<br />

rabbits could be immunized to their own thyroid protein<br />

overturned the established dogma of “horror autotoxicus”<br />

and showed unequivocally that autoimmunity could cause<br />

disease. He and Witebsky also demonstrated that patients<br />

with chronic thyroiditis develop similar antibodies to their<br />

own thyroid antigens, implicating autoimmunity as the cause<br />

of this disease. The initial experiments were followed by others<br />

that elucidated the pathogenesis of autoimmune diseases<br />

Noel Richard Rose (left) with Ernest Witebsky (right).<br />

in animals and humans. In the 1970s he described the critical<br />

role of genetics in conferring susceptibility to autoimmune<br />

disease and showed that the major histocompatibility<br />

complex includes the major susceptibility gene. In the 1980s,<br />

he demonstrated how virus infections can serve as triggers<br />

for autoimmune heart disease. His discoveries opened the<br />

way to improved treatments and new prevention strategies<br />

for this group of diseases. Rose’s pioneering investigations<br />

initiated the modern era of autoimmune disease research. He<br />

served as a professor of microbiology at the State University<br />

of New York at Buffalo, professor and chair of immunology<br />

and microbiology at Wayne State University, Detroit, and<br />

professor and chair of immunology and infectious diseases at<br />

The Johns Hopkins University. The author of more than 675<br />

articles and chapters and editor of many books and leading<br />

journals, he presently directs The Johns Hopkins Center<br />

for Autoimmune Disease Research and the WHO/PAHO<br />

Collaborating Center for Autoimmune Disorders.<br />

Rose–Waaler test<br />

Sheep red blood cells are treated with a subagglutinating<br />

quantity of rabbit anti-sheep erythrocyte antibody. These<br />

particles may be used to identify rheumatoid factor in the<br />

sera of rheumatoid arthritis patients. Agglutination of the<br />

IgG-coated red cells constitutes a positive test and is based<br />

T lymphocyte<br />

CD2<br />

CD2 (ε)<br />

receptor<br />

Sheep<br />

erythrocyte<br />

Adhesion of T lymphocyte and sheep red blood cell.<br />

R

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