PMID- 8978959 OWN - NLM STAT- MEDLINE DCOM- 19970314 LR - 20170112 IS - 0392-856X (Print) IS - 0392-856X (Linking) VI - 14 IP - 6 DP - 1996 Nov-Dec TI - Tumor necrosis factor-alpha (TNF-alpha) in loosening of total hip replacement (THR). PG - 643-8 AB - OBJECTIVE: The initially well-fixed implants of total hip replacement (THR) are in the long-term subject to aseptic loosening. Many cytokines can contribute to osteolysis due to osteoclast recruitment and/or activation. However, in this respect tumor necrosis factor-alpha (TNF-alpha) plays a pivotal role, because it upregulates interleukin-1 and 6 and granulocyte-macrophage colony stimulating factor. The aim of this study was to assess the eventual presence, cellular localization and extent of expression of TNF-alpha in the synovial-like membrane at the implant or at the cement to bone interface compared to control synovial membrane. METHODS: Twenty samples from the synovial-like membrane of the periprosthetic tissues were compared to control samples. TNF-alpha containing cells were visualized using an avidin-biotin-peroxidase complex (ABC) method and analyzed by light microscopy, double labelling and image analysis. RESULTS: TNF-alpha was found in the periprosthetic tissues in fibroblasts and vascular endothelial cells, but mainly in the macrophages was it found to coincide with areas containing implant-derived debris. TNF-alpha containing cells were more numerous in the synovial-like membrane in the interface tissue from the proximal stem area (2816 +/- 318 cells) than in the control synovial membrane (565 +/- 93 cells, p < 0.01). Interestingly, similarly high TNF-alpha expression (3452 +/- 582 cells) was also seen in the synovial-like membrane of the pseudocapsule. CONCLUSION: These findings suggest that the foreign body-type host reaction caused by THR is characterized by the high expression of TNF-alpha. Because such expression occurred in the interface tissue between the implant and surrounding bone, TNF-alpha, due to its pivotal direct and indirect role in the activation and recruitment of osteoclasts, may contribute to periprosthetic osteolysis and to the loosening of THR. FAU - Xu, J W AU - Xu JW AD - Research Unit of the Orthopaedic Hospital, Invalid Foundation, Helsinki, Finland. FAU - Konttinen, Y T AU - Konttinen YT FAU - Lassus, J AU - Lassus J FAU - Natah, S AU - Natah S FAU - Ceponis, A AU - Ceponis A FAU - Solovieva, S AU - Solovieva S FAU - Aspenberg, P AU - Aspenberg P FAU - Santavirta, S AU - Santavirta S LA - eng PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - Italy TA - Clin Exp Rheumatol JT - Clinical and experimental rheumatology JID - 8308521 RN - 0 (Tumor Necrosis Factor-alpha) SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - Endothelium, Vascular/metabolism MH - Female MH - Fibroblasts/metabolism MH - *Hip Prosthesis MH - Humans MH - Immunohistochemistry MH - Macrophages/metabolism MH - Male MH - Middle Aged MH - Osteolysis/*metabolism/pathology/surgery MH - *Prosthesis Failure MH - Reoperation MH - Synovial Membrane/metabolism/pathology MH - Tumor Necrosis Factor-alpha/*metabolism EDAT- 1996/11/01 00:00 MHDA- 1996/11/01 00:01 CRDT- 1996/11/01 00:00 PHST- 1996/11/01 00:00 [pubmed] PHST- 1996/11/01 00:01 [medline] PHST- 1996/11/01 00:00 [entrez] PST - ppublish SO - Clin Exp Rheumatol. 1996 Nov-Dec;14(6):643-8.