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CARDIOVASCULAR
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Volume 3, 1998, No 2 |
Abstract:
Human intravenous immunoglobulins (IVIg) have been successfully
used in different xenotransplant models such as pig to primate or
guinea-pig to rat in order to prevent hyperacute xenograft
rejection (HAR). In this study we analyse the potential
interactions of IVIg with the main actors of HAR such as
xenonatural antibodies (XNA), complement (through the classical
or alternate pathways) activation, and endothelial cell
activation. We demonstrate that IVIg infusion induces a major
decrease of complement activity, through fluid-phase activation
of the complement cascade. IVIg also inhibits XNA binding to
endothelial cells through idiotype/anti-idiotype interactions.
Last, IVIg can also modulate endothelial cell activation. Some of
those mechanisms have been demonstrated to be effective in vivo.
A precise understanding of the mechanisms at play could help
devise more potent preparations of IVIg to be used in future
clinical trials.
Keywords:
xenotransplantation, IVIg, complement, natural antibodies,
idiotypes
Address for Correspondence:
Reference:
(CVE. 1998; 3 (2): 112-119)
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