Skip Navigation


Rheumatology Advance Access originally published online on March 31, 2003
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
42/8/935    most recent
keg255v1
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 (21)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Uhm, W.-S.
Right arrow Articles by Yoo, D.-H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Uhm, W.-S.
Right arrow Articles by Yoo, D.-H.
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?

Rheumatology 2003; 42: 935-938
© 2003 British Society for Rheumatology

Cytokine balance in kidney tissue from lupus nephritis patients

W.-S. Uhm1,4,*, K. Na1,*, G.-W. Song3, S.-S. Jung1, T. Lee2, M.-H. Park3 and D.-H. Yoo1,

1 Hospital for Rheumatic Diseases,
2 Department of Urology, College of Medicine, Hanyang University and
3 Department of Pathology, College of Medicine, Hanyang University, Seoul, Korea
4 Present address: Division of Rheumatology, Department of Internal Medicine, Soonchunhyang University Boocheon Hospital, Boocheon, Korea

Objective. To identify the balance of Th1/Th2 cytokine expression in the kidney and evaluate the difference in cytokine balance between patients with lupus nephritis WHO classes IV and V.

Methods. The expression of the CD40 molecule on cultured human mesangial cells was assessed by flow cytometry after stimulation with interferon {gamma} (IFN-{gamma}) or other cytokines. Frozen sections of kidney tissue from 10 patients with lupus nephritis and two non-SLE patients (with minimal-change disease) were stained with monoclonal antibodies for interleukin (IL)-4, IL-10, IL-12, IFN-{gamma}, CD4, CD8, CD40, CD68 and CD40L.

Results. CD40 expression of cultured mesangial cells was up-regulated by IFN-{gamma}, but was not down-regulated in the presence of the Th2 cytokines IL-4 and IL-10. In the glomeruli, CD40 expression and the ratios of IFN-{gamma}-/IL-10-, IL-12-/IL-4- and (IFN-{gamma}+IL-12)/(IL-4+IL-10)-positive cells were significantly higher in class IV than in class V lupus nephritis (P < 0.05). Also CD40, IFN-{gamma} and the activity index derived from the renal biopsy were closely correlated.

Conclusion. IFN-{gamma} may contribute to the pathogenesis of proliferative glomerulonephritis by the up-regulation of CD40 and the activation of the cellular immune response in human lupus.

KEY WORDS: Systemic lupus erythematosus, Cytokine, Interferon-{gamma}, Lupus nephritis, CD40.

* These two authors contributed equally to this manuscript

Correspondence to: D.-H. Yoo, Hospital for Rheumatic Diseases, Hanyang University, Seoul 133-792, Korea. E-mail: dhyoo{at}hanyang.ac.kr


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


This article has been cited by other articles:


Home page
J. Immunol.Home page
M. Harigai, M. Kawamoto, M. Hara, T. Kubota, N. Kamatani, and N. Miyasaka
Excessive Production of IFN-{gamma} in Patients with Systemic Lupus Erythematosus and Its Contribution to Induction of B Lymphocyte Stimulator/B Cell-Activating Factor/TNF Ligand Superfamily-13B
J. Immunol., August 1, 2008; 181(3): 2211 - 2219.
[Abstract] [Full Text] [PDF]



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.