Raised intrathecal levels of APRIL and BAFF in patients with systemic lupus erythematosus relationship to neuropsychiatric symptoms 英文参考文献.docVIP
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Raised intrathecal levels of APRIL and BAFF in patients with systemic lupus erythematosus relationship to neuropsychiatric symptoms 英文参考文献
Available online /content/10/4/R97
Research article
Open Access
Vol 10 No 4
Raised intrathecal levels of APRIL and BAFF in patients with
systemic lupus erythematosus: relationship to neuropsychiatric
symptoms
Annie George-Chandy1,2, Estelle Trysberg3 and Kristina Eriksson1
1Department of Rheumatology and Inflammation Research, Guldhedsgatan 10A, 413 46 Gothenburg, Sweden
2Department of Infection Immunology, Statens Serum Institut, Artillerivej 5, 232 300 Copenhagen, Denmark
3Rheumatogy Unit at Karolinska University Hospital/Huddinge, H?lsov?gen 141, 141 52 Huddinge, Sweden
Corresponding author: Annie George-Chandy, annie.george.chandy@microbio.gu.se
Received: 2 Apr 2008 Revisions requested: 29 Apr 2008 Revisions received: 28 Jul 2008 Accepted: 22 Aug 2008 Published: 22 Aug 2008
Arthritis Research Therapy 2008, 10:R97 (doi:10.1186/ar2484)
This article is online at: /content/10/4/R97
? 2008 George-Chandy et al.; licensee BioMed Central Ltd.
This is an open access article distributed under the terms of the Creative Commons Attribution License (/licenses/by/2.0),
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract
Introduction The tumour necrosis factor (TNF) family ligands
BAFF (B-cell activating factor of TNF family) and APRIL (a
proliferation-inducing ligand) are essential for B-cell survival and
function. Elevated serum levels of BAFF and APRIL have been
reported earlier in patients with systemic lupus erythematosus
(SLE). Since autoantibody formation in the central nervous
system (CNS) is a distinct feature of neuropsychiatric SLE
(NPSLE), we have investigated whether NPSLE is associated
with an enhanced intrathecal production of APRIL and BAFF.
Separate analyses of SLE patients with and without CNS
involvement revealed that NPSLE patients had enhanced levels
of APRIL in CSF. BAFF and APRIL were likely produced locally
in the CNS
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