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Antibody cross-reactivity

There is considerable interest in the role of infectious agents in the development of autoimmune diseases. Some of this interest is based on the concept of molecular mimicry as a causal mechanism. Molecular mimicry refers to the possible pathologic role of cross-reactive antibodies or T cells to a self-antigen that is structurally similar to, and thus shares epitopes with, a viral or other infectious agent. For most autoimmune diseases, however, evidence of molecular mimicry leading to disease is not conclusive.1819 Viruses and other infections also have a less-specific immune effect, stimulating toll-like receptors and proinflammatory cytokine secretion, which is another mechanism that has been postulated to influence autoimmune disease risk.20... [Pg.440]

A 54-year-old woman with type 2 diabetes had poor metabolic control, despite using 60-80 units of shortacting and long-acting human insulins for 10 years (34). Transfer to insulin lispro reduced the daily amount of insulin to 28 units. Insulin specific antibodies fell from 2.7 to 0.3% and cross-reactive antibodies, binding both human insulin and insulin lispro, fell from 44 to 16%. Specific insulin lispro antibodies rose from 0 to 0.3%. HbAic fell from 9.1% to 6.8% and body mass index from 30 to 27, probably because of the reduced dose of insulin. [Pg.430]

Cross-Reactive Antibody. The ability of anti-DNA antibodies to bind to other negatively charged substances represents an attractive variant of the... [Pg.149]

Muller-Loennies, S., Brade, L., Brade, H. Neutralizing and cross-reactive antibodies against enterobacterial lipopolysaccharide. Int J Med Microbiol 297 (2007) 321-340. [Pg.301]

Monoclonal antibodies generated with purified Uri eliminated crossreaction to THP and Iof in urine and plasma, respectively. Antibodies directed at the N-linked glycan allowed measurement of Bik in blood without IqI cross-reactivity. Antibodies directed at the peptide allowed measurement of urinary Bik without THP cross-reactivity. These antibodies do not cross-react with aprotinin. These antibodies allow estimating the Iof family in blood. [Pg.234]

Ang CW, Jacobs BC, Brandenburg AH, Laman JD, van der Meche FGA, Osterhaus ADME, Van Doom PA (2000) Cross-reactive antibodies against GM2 and CMV-infected fibroblasts in Guillain-BaiTe syndrome. Neurology 54 1453—1458. [Pg.275]

Jacobs BC, Hazenberg MP, Van Doom PA, Endtz HPh, van der Meche FGA (1997) Cross-reactive antibodies against gangbosides and Campylobacter jejuni bpopolysaccharides in patients with GnUlain-Barre or Miller Fisher syndrome. J Inf Dis 175 729-733. [Pg.278]

B27, the HLA allele proposed to be involved in alkylosing spondylitis, shares an epitope with an enzyme from Klebsiella pneumoniae, a common intestinal Gram negative bacterium. Molecular mimicry is thought to result in cross-reactive antibody formation, joint inflammation and spinal damage. Along with many of the immunotherapies described for other similar arthritic autoimmune disorders, alkylosing spondylitis is treated with anti-inflammatory medications and a low carbohydrate diet to reduce intestinal K. pneumoniae levels. [Pg.289]

Fig. 8.4. Concepts of shared (I) and cross-reactivity (II). Two antigens (A and B) may have one or more identical epitopes and a subpopulation of antibodies from a polyclonal antiserum will react equally with both antigens (shared reactivity). If monoclonal antibodies against the common epitope were used, it would not be possible to distinguish A and B. In cross-reactivity, antibodies reactive with the homologous antigen are also reactive with different epitopes (generally less fit thus lower affinity). Fig. 8.4. Concepts of shared (I) and cross-reactivity (II). Two antigens (A and B) may have one or more identical epitopes and a subpopulation of antibodies from a polyclonal antiserum will react equally with both antigens (shared reactivity). If monoclonal antibodies against the common epitope were used, it would not be possible to distinguish A and B. In cross-reactivity, antibodies reactive with the homologous antigen are also reactive with different epitopes (generally less fit thus lower affinity).
The third category, 2° antibody, summarizes 2° antibody and label information. This information allows the scientist to check the species of the 2° antibodies so that no cross-reactive antibodies will be used. In addition, the information about the fluorophores lists the excitation and emission wavelengths to show that different nonoverlapping fluorophores will be used. [Pg.93]

The evolutionary relations among subunits of F from several sources were tested by immunological cross-reactivity. Antibodies raised against subunits of Fi were reacted with H -ATPase complex from Chlamydomonas and spinach chloroplasts, from beef adrenal, rat liver and yeast mitochondria and with E. coli membranes. The antigen-antibody reaction was tested employing the electrotransfer technique (Rott, Nelson 1981 Towbin et al. 1979). The antibodies employed were raised against the following subunits of the H -ATPase complex o(,, < and... [Pg.502]


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Antibody Cross-Reactivity and Molecular Mimicry

Cross reactivity

Cross reactivity analysis antibody specificity

Cross-reactivity characterization specific antibody

Cross-reactivity studies antibodies

Cross-reactivity studies monoclonal antibodies

Cross-reactivity, of antibody

Monoclonal antibodies cross-reactivity

Monoclonal antibody tissue cross-reactivity

Tissue cross-reactivity assay monoclonal antibodies

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