Titlebook: Immunobiology of Proteins and Peptides VII; Unwanted Immune Resp M. Zouhair Atassi Book 1994 The Editor(s) (if applicable) and The Author(s

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Stress Proteins in Autoimmunity, five principal observations. First, stress proteins are immunodominant antigens of all prokaryotic infectious microorganisms, many of which have been implicated as inducers of arthritis and autoimmune disease in genetically susceptible individuals. Second, the T-cell repertoire, especially that of

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Polyclonal B Cell Activation and B Cell Cross-Reactivity During Autoantibody Production in Systemicy production is induced and maintained. The first holds that specific autoantigens (or antigens cross-reactive with self) stimulate an anti-self response (i.e., DNA inducing anti-DNA antibodies).. The second proposes that autoantibody production results from a generalized process of antigen-independ

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Regulatory Autoantibody and Cellular Aging and Removal,. It acts as a specific signal for cellular termination by initiating the binding of IgG autoantibody and subsequent removal by phagocytes (Kay, 1975, 1978,1981, 1984, 1983, 1986, 1988a, 1988b, 1988c, 1990; Kay .., 1986, 1989, 1982, 1983a, 1988a, 1988b,1991, 1990a, 1990b, 1990c, 1990d; Kay and Lin,

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B-Cell Origin of Cold Agglutinins,ficance. Virtually all sera from healthy individuals contain low titered CA which cause no apparent immune hemolysis and may be defined as natural or benign RBC autoantibodies. In contrast, the pathologic (e.g. hemolytic) counterparts of these autoantibodies are generally derived from clonal B cell

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Initiation of Autoimmune Type 1 Diabetes and Molecular Cloning of a Gene Encoding for Islet Cell-Spiling only cancer and cardiovascular disease. There are two major forms of diabetes mellitus. One is type I diabetes, which is also known as insulin-dependent diabetes mellitus (IDDM), and the other is type II diabetes, which is also known as noninsulin-dependent diabetes mellitus (NIDDM). Most pati

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,Mapping of the Polypeptide Chain Organization of the Main Extracellular Domain of the α-Subunit in ned the ability of the native membrane-bound AChR of . (T-AChR) to bind a panel of antibodies against overlapping synthetic peptides which collectively encompassed this entire domain. Antibodies against the α-chain peptides αl–16, α89–104 and α158–174 were able to bind to membrane-bound T-AChR. Othe

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