Objective. To determine whether silicone implantation exacerbates autoimmune disease in a murine experimental model of arthritis.Methods. DBA/l mice were implanted with silicone in the form of an elastomer, gel, or oil, and immunized with type I1 collagen. The influence of silicone implantation on collagen-induced arthritis and the immune response to type I1 collagen were determined by comparison against control mice receiving sham implantation. Adjuvant effects of silicone implantation were examined by measuring cytokine levels in implanted animals and assessing autoantibodies against proteins extracted from recovered silicone implants.Results. No adverse influence of silicone implantation on the clinical aspects of collagen-induced arthritis was observed. Further, polydimethylsiloxane silicone oil failed to serve as an adjuvant in the immune or arthritogenic response to type I1 collagen in mice. Cytokine analysis indicated that tumor necrosis factor a levels were lower and interleukin-2 levels were higher in silicone-implanted mice. The development of arthritis increased protein binding to implanted elastomers and gel, and autoantibodies against silicone-bound proteins were present in sera from arthritic mice and absent in sera from nonarthritic mice.Conclusion. The data suggest that silicone implantation may result in autoantibodies against silicone-bound proteins, and the presence of arthritis may either provoke or increase the level of such autoantibodies. However, silicone implantation did not inMs. Schaefer is the recipient of a Graduate Research Assistantship provided by Hutzel Hospital.