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Background. Neutrophils have been shown to play a role in ischemia-reperfusion injury, and the
initial interaction of neutrophils with the endothelium is mediated through the selectin
family of adhesion molecules. Thus the purpose of these studies was to determine whether
a P-selectin-IgG chimera was protective in a model of ischemia-reperfusion injury.
Methods. The model used was a rabbit ear model of ischemia-reperfusion. Selectin-IgG chimeras
were given at the time of reperfusion of the tissue, and their efficacy was compared
with an anti-CD18 antibody (MHM23).
Results. The P-selectin-IgG was as protective in this model as an anti-CD18 antibody. The
chimera did not mediate its effect by causing the animals to become neutropenic.
Conclusions. P-selectin plays a role in ischemia-reperfusion injury. This is in agreement with
data from other groups. The fact that the chimera was effective in this model suggests
that carbohydrates or small molecule mimics of carbohydrates would be effective in
this model. Such antiinflammatory agents may have fewer side effects in terms of increased
risk of sepsis.
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Article info
Publication history
Accepted:
September 26,
1994
Identification
Copyright
© 1995 Mosby-Year Book, Inc. Published by Elsevier Inc.