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Proteomic shifts post-plasma cell therapy in AL amyloid plaques and potential implications for light chaindirected

Matthew J Rees1, Surendra Dasari2, Ellen D McPhail3

  • 1Division of Hematology, Mayo Clinic, Rochester, MN. Rees.Matthew@mayo.edu.

Haematologica
|July 24, 2025
PubMed
Abstract

No abstract available in PubMed .

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Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
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