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Published in: Clinical Reviews in Allergy & Immunology 2-3/2010

01-04-2010

Currents Concepts on the Immunopathology of Amyloidosis

Authors: Anupama Bhat, Carlo Selmi, Stanley M. Naguwa, Gurtej S. Cheema, M. Eric Gershwin

Published in: Clinical Reviews in Allergy & Immunology | Issue 2-3/2010

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Abstract

Amyloidosis is defined as the extracellular accumulation at systemic or organ-specific level of insoluble low molecular weight protein fibrils manifesting a beta pleated sheet configuration and a characteristic staining pattern. Several different types of proteins may lead to this phenomenon, and amyloidosis is defined by the biochemical nature of the protein in the deposits and further classified according to whether the deposits are localized or systemic, acquired or inherited, and by the resulting clinical phenotype. Amyloidosis includes subtypes such as light chain, associated with serum amyloid A protein, heritable and familial forms, dialysis-related disease, and organ-specific conditions. The pathogenesis and clinical features of these clinical and pathological entities will be critically discussed in this review article.
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Metadata
Title
Currents Concepts on the Immunopathology of Amyloidosis
Authors
Anupama Bhat
Carlo Selmi
Stanley M. Naguwa
Gurtej S. Cheema
M. Eric Gershwin
Publication date
01-04-2010
Publisher
Humana Press Inc
Published in
Clinical Reviews in Allergy & Immunology / Issue 2-3/2010
Print ISSN: 1080-0549
Electronic ISSN: 1559-0267
DOI
https://doi.org/10.1007/s12016-009-8163-9

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