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Prospective analysis of human leukocyte functional tests reveals metal sensitivity in patients with hip implant
BACKGROUND: The aim of the study was to examine the reactivity of peripheral human leukocytes to various metal ions prior and following hip replacement in order to investigate implant-induced metal sensitivity. METHODS: Three patient groups were set up: (1) individuals without implants and no histor...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674931/ https://www.ncbi.nlm.nih.gov/pubmed/23680415 http://dx.doi.org/10.1186/1749-799X-8-12 |
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author | Vermes, Csaba Kuzsner, József Bárdos, Tamás Than, Péter |
author_facet | Vermes, Csaba Kuzsner, József Bárdos, Tamás Than, Péter |
author_sort | Vermes, Csaba |
collection | PubMed |
description | BACKGROUND: The aim of the study was to examine the reactivity of peripheral human leukocytes to various metal ions prior and following hip replacement in order to investigate implant-induced metal sensitivity. METHODS: Three patient groups were set up: (1) individuals without implants and no history of metal allergy (7 cases), (2) individuals without implants and known history of metal allergy (7 cases), and (3) patients undergoing cementless hip replacement (40 cases). Blood samples were taken in groups 1 and 2 at three different occasions; in group 3, prior and 3, 6, 12, 24, and 36 months after surgery. Peripheral leukocytes were separated and left either untreated or challenged with Ti, NiCl(2), CoCl(2), CrCl(3), and phytohemagglutinin. Cell proliferation, cytokine release, and leukocyte migration inhibition assays were performed. Metal-induced reactivity was considered when all three assays showed significant change. Skin patch tests were also carried out. RESULTS: Both skin patch tests and leukocyte functional tests were negative in group 1, and both were positive in group 2. In group 3, after 6 months, 12% of the patients showed reactivity to the tested metals except for NiCl(2). Following the 36-month period, 18% of group three became sensitive to metals (including all the earlier 12%). In contrast, patch tests were negative at each time point in group 3. CONCLUSIONS: Orthopedic implant material may induce metal reactivity after implantation in a manner where susceptibility is yet to be elucidated. Leukocyte triple assay technique might be a useful tool to test implant material-related sensitivity. |
format | Online Article Text |
id | pubmed-3674931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36749312013-06-07 Prospective analysis of human leukocyte functional tests reveals metal sensitivity in patients with hip implant Vermes, Csaba Kuzsner, József Bárdos, Tamás Than, Péter J Orthop Surg Res Research Article BACKGROUND: The aim of the study was to examine the reactivity of peripheral human leukocytes to various metal ions prior and following hip replacement in order to investigate implant-induced metal sensitivity. METHODS: Three patient groups were set up: (1) individuals without implants and no history of metal allergy (7 cases), (2) individuals without implants and known history of metal allergy (7 cases), and (3) patients undergoing cementless hip replacement (40 cases). Blood samples were taken in groups 1 and 2 at three different occasions; in group 3, prior and 3, 6, 12, 24, and 36 months after surgery. Peripheral leukocytes were separated and left either untreated or challenged with Ti, NiCl(2), CoCl(2), CrCl(3), and phytohemagglutinin. Cell proliferation, cytokine release, and leukocyte migration inhibition assays were performed. Metal-induced reactivity was considered when all three assays showed significant change. Skin patch tests were also carried out. RESULTS: Both skin patch tests and leukocyte functional tests were negative in group 1, and both were positive in group 2. In group 3, after 6 months, 12% of the patients showed reactivity to the tested metals except for NiCl(2). Following the 36-month period, 18% of group three became sensitive to metals (including all the earlier 12%). In contrast, patch tests were negative at each time point in group 3. CONCLUSIONS: Orthopedic implant material may induce metal reactivity after implantation in a manner where susceptibility is yet to be elucidated. Leukocyte triple assay technique might be a useful tool to test implant material-related sensitivity. BioMed Central 2013-05-16 /pmc/articles/PMC3674931/ /pubmed/23680415 http://dx.doi.org/10.1186/1749-799X-8-12 Text en Copyright © 2013 Vermes et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Vermes, Csaba Kuzsner, József Bárdos, Tamás Than, Péter Prospective analysis of human leukocyte functional tests reveals metal sensitivity in patients with hip implant |
title | Prospective analysis of human leukocyte functional tests reveals metal sensitivity in patients with hip implant |
title_full | Prospective analysis of human leukocyte functional tests reveals metal sensitivity in patients with hip implant |
title_fullStr | Prospective analysis of human leukocyte functional tests reveals metal sensitivity in patients with hip implant |
title_full_unstemmed | Prospective analysis of human leukocyte functional tests reveals metal sensitivity in patients with hip implant |
title_short | Prospective analysis of human leukocyte functional tests reveals metal sensitivity in patients with hip implant |
title_sort | prospective analysis of human leukocyte functional tests reveals metal sensitivity in patients with hip implant |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674931/ https://www.ncbi.nlm.nih.gov/pubmed/23680415 http://dx.doi.org/10.1186/1749-799X-8-12 |
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