A frequent long-term complication of total joint arthroplasty is aseptic lo
osening, the end result of wear debris accumulation, synovitis, and osteoly
sis about the implant-bone or cement-bone interface. Complement, an effecto
r system in plasma, synovial fluid, and tissue, has powerful chemotactic, i
nflammatory, and osteoclast-activating potentials. This study explored the
complement-activating ability of polyethylene, a material used in joint Imp
lants. In vitro hemolytic assays using sheep red blood cells (E-sh), human
serum, and particulate polyethylene suggested alternative pathway complemen
t activation, as well as polyethylene adsorption of activated complement co
mponents. These results were confirmed by enzyme-linked immunosorbent assay
(ELISA) quantification of activated complement factors Bb and C3b. In situ
double antibody immunoperoxidase staining for factors Bb, C3a, iC3b, and S
C5-9 in synovial tissue from revision hip specimens showed localized altern
ative pathway activation and component adsorption. These results introduce
a likely role for complement activation in particle-mediated recruitment, p
roliferation, and activation of macrophages during early events in osteolys
is and implant loosening. (C) 2000 John Wiley & Sons, Inc.