By P. A. Muraro, A. Lugaresi, D. Gambi (auth.), D. Gambi, P. A. Muraro, A. Lugaresi, U. Ecari (eds.)
P.A. MURARO, A. LUGARESI, D. GAMBI a number of the pathological elements of a number of sclerosis (MS) lesions were identified for over a century. it is just lately, despite the fact that, that assorted styles of demyelination were associated with exact pathways of immune-mediated tissue destruction. particularly, the inter-individual heterogeneity of MS lesions has instructed that diverse mechanisms could act in numerous sufferers, accounting for the range saw in scientific path, immunological findings in peripheral blood and cere brospinal fluid (CSF), and reaction to immunomodulatory remedies. to supply an summary of the elemental mechanisms potentially interested by MS lesion initiation and improvement, a global assembly was once geared up within the context of the once a year Congress of the Italian Neuroimmunology organization (AINI), held on the college of Chieti, in Chieti Italy on 29 October 1998. The excessive ordinary of shows triggered us to document them in prolonged shape, to focus on fresh seasoned gress within the figuring out of simple mechanisms maintaining MS immuno pathogenesis. A valuable function within the attainable mechanisms resulting in myelin destruc tion has been attributed to T lymphocytes reactive to myelin antigens. reports at the myelin antigen-specific T phone repertoire have contributed major advances to our wisdom of autoimmunity (Chapters 1,2).
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Additional info for Advances in the Immunopathogenesis of Multiple Sclerosis
Recently we demonstrated that peptides deduced from these motifs, containing optimal amino acids in each individual position, were highly stimulatory for the individual TCC . In addition we were able to define crossreactive antigens from non-self sources that stimulated the TCCs at higher potency than the self-peptide MBP . This observation demonstrated that the PS-SCL approach allow precise determination of TCR motifs and identification of potent peptide ligands. 28 fM and less (PS-SCL concentration 100 Jlg/ml and less) demonstrated the flexibility of the TCR recognition of those TCC.
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