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RP105-Negative B Cells in Systemic Lupus Erythematosus

Systemic lupus erythematosus (SLE) is a multisystem disease characterized by B cells producing autoantibodies against nuclear proteins and DNA, especially anti-double-strand DNA (dsDNA) antibodies. RP105 (CD180), the toll-like receptor- (TLR-) associated molecule, is expressed on normal B cells. How...

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Detalles Bibliográficos
Autores principales: Koarada, Syuichi, Tada, Yoshifumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3175410/
https://www.ncbi.nlm.nih.gov/pubmed/21941580
http://dx.doi.org/10.1155/2012/259186
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author Koarada, Syuichi
Tada, Yoshifumi
author_facet Koarada, Syuichi
Tada, Yoshifumi
author_sort Koarada, Syuichi
collection PubMed
description Systemic lupus erythematosus (SLE) is a multisystem disease characterized by B cells producing autoantibodies against nuclear proteins and DNA, especially anti-double-strand DNA (dsDNA) antibodies. RP105 (CD180), the toll-like receptor- (TLR-) associated molecule, is expressed on normal B cells. However, RP105-negative B cells increase in peripheral blood from patients with active SLE. RP105 may regulate B-cell activation, and RP105-negative B cells produce autoantibodies and take part in pathophysiology of SLE. It is possible that targeting RP105-negative B cells is one of the treatments of SLE. In this paper, we discuss the RP105 biology and clinical significance in SLE.
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spelling pubmed-31754102011-09-22 RP105-Negative B Cells in Systemic Lupus Erythematosus Koarada, Syuichi Tada, Yoshifumi Clin Dev Immunol Review Article Systemic lupus erythematosus (SLE) is a multisystem disease characterized by B cells producing autoantibodies against nuclear proteins and DNA, especially anti-double-strand DNA (dsDNA) antibodies. RP105 (CD180), the toll-like receptor- (TLR-) associated molecule, is expressed on normal B cells. However, RP105-negative B cells increase in peripheral blood from patients with active SLE. RP105 may regulate B-cell activation, and RP105-negative B cells produce autoantibodies and take part in pathophysiology of SLE. It is possible that targeting RP105-negative B cells is one of the treatments of SLE. In this paper, we discuss the RP105 biology and clinical significance in SLE. Hindawi Publishing Corporation 2012 2011-09-15 /pmc/articles/PMC3175410/ /pubmed/21941580 http://dx.doi.org/10.1155/2012/259186 Text en Copyright © 2012 S. Koarada and Y. Tada. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Koarada, Syuichi
Tada, Yoshifumi
RP105-Negative B Cells in Systemic Lupus Erythematosus
title RP105-Negative B Cells in Systemic Lupus Erythematosus
title_full RP105-Negative B Cells in Systemic Lupus Erythematosus
title_fullStr RP105-Negative B Cells in Systemic Lupus Erythematosus
title_full_unstemmed RP105-Negative B Cells in Systemic Lupus Erythematosus
title_short RP105-Negative B Cells in Systemic Lupus Erythematosus
title_sort rp105-negative b cells in systemic lupus erythematosus
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3175410/
https://www.ncbi.nlm.nih.gov/pubmed/21941580
http://dx.doi.org/10.1155/2012/259186
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