Volume 6 Supplement 1

15thPaediatric Rheumatology European Society (PreS) Congress

Open Access

2.5 Mesenchymal Stem Cell Therapy has significant clinical effect in proteoglycan induced arthritis

  • JF Swart2,
  • MJG Backer3,
  • F Hofhuis3,
  • W de Jager1,
  • BJ Prakken1,
  • W Kuis1,
  • ACM Martens3 and
  • NM Wulffraat1
Pediatric Rheumatology20086(Suppl 1):S5

DOI: 10.1186/1546-0096-6-S1-S5

Published: 15 September 2008

Introduction

Mesenchymal Stem Cells (MSC) are adult stem cells which are mainly present in bone marrow and fat. The cell is a fine candidate for treatment of juvenile idiopathic arthritis since it has strong immunosuppressive activities in vitro as well as in vivo [1, 2].

Methods

We performed a study with 104 Balb/c mice with 55 as donors of MSC. The 49 mice that were induced twice with human proteoglycan for the development of PGIA were randomly assigned to 5 groups: 1 control-group (PBS) and 4 treatment-groups (MSC once or twice intraperitoneal [ip] or intra-articular [ia]). Ten days after 2nd PG-antigen injection, treatment was started and if planned again after 4 weeks. Dosages were 5 × 106 ip and 1 × 106 cells ia. MSC used were syngeneic and passaged twice. Arthritis was scored 2 times a week by 2 independent observers according to a scoringsystem with a maximum of 16.

Results

Arthritis-score was on average 1.3 (0.8–2.0) just before start of the treatment and increased to 6.0 in the control group towards the end of the experiment (day 67). At day 67 arthritis-scores were significantly lower in both ip-groups (1.0 and 0.5) and in the repeated ia-group (2.0). Furthermore in both ip-groups arthritis-scores decreased after treatment and stabilized until day 67.

Conclusion

High dose MSC systemically administered (ip) has good clinical effect on established arthritis. Arthritisscore not only stabilized but even diminished after injection of ip MSC. Ip injection of MSC once was as good as twice; this was not true for the ia injection.

Authors’ Affiliations

(1)
Department of Pediatric Immunology, Wilhelmina Children's Hospital/UMC Utrecht
(2)
VU University Medical Center
(3)
Department of Immunology, UMC Utrecht

References

  1. Uccelli A: Eur J Imm. 2006Google Scholar
  2. Le Blanc K: Lancet. 2004Google Scholar

Copyright

© Swart et al; licensee BioMed Central Ltd. 2008

This article is published under license to BioMed Central Ltd.

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