Differential clinical efficacy of anti-CD4 monoclonal antibodies in rat adjuvant arthritis is paralleled by differential influence on NF-κB binding activity and TNF-α secretion of T cells.docVIP
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Differential clinical efficacy of anti-CD4 monoclonal antibodies in rat adjuvant arthritis is paralleled by differential influence on NF-κB binding activity and TNF-α secretion of T cells
Available online /content/4/3/184
Research article
Differential clinical efficacy of anti-CD4 monoclonal antibodies in
rat adjuvant arthritis is paralleled by differential influence on
κ
α
NF- B binding activity and TNF- secretion of T cells
Dirk Pohlers1, Carsten B Schmidt-Weber2, Angels Franch3, Jürgen Kuhlmann4, Rolf Br?uer5,
Frank Emmrich6 and Raimund W Kinne1
1Experimental Rheumatology Unit, Friedrich Schiller University, Jena, Germany
2Swiss Institute of Asthma and Allergy Research (SIAF), Davos, Switzerland
3Faculty of Pharmacy, University of Barcelona, Barcelona, Spain
4Max Planck Institute of Molecular Physiology, Dortmund, Germany
5Institute of Pathology, Friedrich Schiller University, Jena, Germany
6Institute of Clinical Immunology and Transfusion Medicine, University of Leipzig, Leipzig, Germany
Correspondence: Raimund W Kinne, MD, Experimental Rheumatology Unit, Friedrich Schiller University, Bachstr 18, D-07740 Jena, Germany.
Tel: +49 3641 657150; fax: +49 3641 657152, e-mail: Raimund.W.Kinne@rz.uni-jena.de
Received: 23 July 2001
Arthritis Res 2002, 4:184-189
Revisions requested: 9 October 2001
Revisions received: 5 November 2001
Accepted: 8 November 2001
Published: 8 January 2002
This article may contain supplementary data which can only be found
online at /content/4/3/184
? 2002 Pohlers et al., licensee BioMed Central Ltd
(Print ISSN 1465-9905; Online ISSN 1465-9913)
Abstract
The aim of this study was to analyze the differential effects of three anti-CD4 monoclonal antibodies
(mAbs) (with distinct epitope specifities) in the treatment of rat adjuvant arthritis (AA) and on T-cell
function and signal transduction. Rat AA was preventively treated by intraperitoneal injection of the
anti-CD4 mAbs W3/25, OX35, and RIB5/2 (on days –1, 0, 3, and 6, i.e. 1 day before AA induction, on
the day of induction [day 0], and thereafter). The effects on T-cell reactivity in vivo (delayed-type
hypersensitivity), ex vivo (concanavalin-
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