Damian Maseda
Post-doctoral Fellow
Last active: 10/12/2016

The proteasome inhibitor bortezomib depletes plasma cells and protects mice with lupus-like disease from nephritis.

Neubert K, Meister S, Moser K, Weisel F, Maseda D, Amann K, Wiethe C, Winkler TH, Kalden JR, Manz RA, Voll RE
Nat Med. 2008 14 (7): 748-55

PMID: 18542049 · DOI:10.1038/nm1763

Autoantibody-mediated diseases like myasthenia gravis, autoimmune hemolytic anemia and systemic lupus erythematosus represent a therapeutic challenge. In particular, long-lived plasma cells producing autoantibodies resist current therapeutic and experimental approaches. Recently, we showed that the sensitivity of myeloma cells toward proteasome inhibitors directly correlates with their immunoglobulin synthesis rates. Therefore, we hypothesized that normal plasma cells are also hypersensitive to proteasome inhibition owing to their extremely high amount of protein biosynthesis. Here we show that the proteasome inhibitor bortezomib, which is approved for the treatment of multiple myeloma, eliminates both short- and long-lived plasma cells by activation of the terminal unfolded protein response. Treatment with bortezomib depleted plasma cells producing antibodies to double-stranded DNA, eliminated autoantibody production, ameliorated glomerulonephritis and prolonged survival of two mouse strains with lupus-like disease, NZB/W F1 and MRL/lpr mice. Hence, the elimination of autoreactive plasma cells by proteasome inhibitors might represent a new treatment strategy for antibody-mediated diseases.

MeSH Terms (16)

Animals Boronic Acids Bortezomib Lupus Erythematosus, Systemic Mice Mice, Inbred BALB C Mice, Inbred MRL lpr Mice, Inbred NZB Models, Immunological Nephritis Ovalbumin Plasma Cells Protease Inhibitors Proteasome Inhibitors Pyrazines Time Factors

Connections (1)

This publication is referenced by other Labnodes entities:

Links