Skip Navigation


Rheumatology Advance Access originally published online on June 16, 2006
Rheumatology 2007 46(1):65-69; doi:10.1093/rheumatology/kel177
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
46/1/65    most recent
kel177v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (11)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Sène, D.
Right arrow Articles by Cacoub, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sène, D.
Right arrow Articles by Cacoub, P.
Related Collections
Right arrow Systemic Lupus Erythematosus and Autoimmunity
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2006. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Hepatitis C virus-associated B-cell proliferation—the role of serum B lymphocyte stimulator (BLyS/BAFF)

D. Sène, N. Limal, P. Ghillani-Dalbin1, D. Saadoun, J.-C. Piette and P. Cacoub

Department of Internal Medicine and 1Department of Immunochemistry, La Pitié-Salpêtrière Hospital, 47-83 Boulevard de l’Hôpital, 75651 Paris cedex 13, France.

Correspondence to: Prof. Patrice Cacoub, MD, Service de Médecine Interne, Hôpital La Pitié-Salpêtrière, 83 Boulevard de l’Hôpital, 75651 Paris Cedex 13, France. E-mail: patrice.cacoub{at}psl.ap-hop-paris.fr


   Abstract

Objective. B lymphocyte stimulator (BLyS) is known to support B-cell proliferation (BCP) in B-cell haemopathies and autoimmune diseases. We assume that BLyS may play a role in the initiation and expression of hepatitis C virus (HCV)-associated BCP. We assessed BLyS serum levels in HCV-infected patients and in various forms of HCV-associated BCP [i.e. mixed cryoglobulin (MC), rheumatoid factor (RF) and systemic vasculitis].

Methods. A total of 76 HCV-infected patients (HCV RNA+) were compared with 13 healthy volunteers. Epidemiological, clinical, immunochemical and virological data were prospectively collected. BLyS serum levels were assessed by an ELISA sandwich method.

Results. Of the 76 patients, 38 females, 38 males, mean age 53 ± 15 yrs; 47 (62%) patients had type II (27 patients) or type III MC (20 patients); 27 (35.5%) patients had HCV-systemic vasculitis. BLyS serum levels tended to be higher in HCV-infected patients than in healthy controls (1.8 ± 0.9 vs 1.5 ± 0.2 ng/ml), were higher in patients with MC than without (2.03 ± 1.02 vs 1.5 ± 0.5 ng/ml; P = 0.008), and even higher in type II than type III MC (2.3 ± 1.2 vs 1.7 ± 0.6 ng/ml; P = 0.03). There was a correlation between BLyS and MC serum levels (R = 0.4; P = 0.004). BLyS serum levels were higher in patients with a positive RF than in those without (2.06 ± 1.09 vs 1.6 ± 0.56 ng/ml, P = 0.035), and with systemic vasculitis than in those without (2.24 ± 1.16 vs 1.6 ± 0.6 ng/ml; P = 0.006).

Conclusion. BLyS serum levels are significantly correlated with B-cell proliferation during chronic HCV infection. These results strongly suggest a role for BLyS in the induction and expression of HCV-BCP.

KEY WORDS: BLyS (BAFF), HCV, B-cell proliferation, Mixed cryoglobulinaemia


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.