Extended reports
Granulocyte-macrophage colony stimulating factor exacerbates
collagen induced arthritis in mice
a University of Melbourne, Department
of Medicine, Royal Melbourne Hospital, Victoria, Australia
, b Amgen Boulder Inc, Boulder, CO, USA
Correspondence to: Dr I K Campbell, University of Melbourne, Department of Medicine, Royal Melbourne Hospital, Parkville, Vic 3050, Australia.
Accepted for publication 3 April 1997
OBJECTIVE
To examine the effect of
granulocyte-macrophage colony stimulating factor (GM-CSF) on disease
progression in the collagen induced arthritis (CIA) model in mice.
METHODS
DBA/1 mice were primed for a suboptimal
CIA response by intradermal injection of chick type II collagen without
a secondary immunisation. Three weeks after immunisation the mice were
given four to five consecutive daily intraperitoneal injections of
recombinant murine GM-CSF (15 µg; 5 × 105 U), or
vehicle, and arthritis development was monitored by clinical scoring of
paws and calliper measurements of footpad swelling. At approximately
six to eight weeks after immunisation mice were killed, their limbs
removed and processed for histological analyses of joint pathology.
RESULTS
Control animals receiving a single
immunisation with collagen exhibited a varied CIA response both in
terms of incidence and severity. Mice treated with GM-CSF at 20 to 25 days after immunisation with collagen had a consistently greater
incidence and more rapid onset of disease than the vehicle treated
control mice, based on clinical assessment. GM-CSF treated mice showed
higher average clinical scores and greater paw swelling than controls.
Histological analyses of joints reflected the clinical scores with
GM-CSF treated mice displaying more pronounced pathology (synovitis,
pannus formation, cartilage and bone damage) than control mice.
CONCLUSION
GM-CSF is a potent accelerator of the
pathological events leading to chronic inflammatory polyarthritis in
murine CIA supporting the notion that GM-CSF may play a part in
inflammatory polyarthritis, such as rheumatoid arthritis.
© 1997 by Annals of the Rheumatic Diseases
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