2021
DOI: 10.5507/bp.2020.019
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The number of lymphocytes increases in the periprosthetic tissues with increasing time of implant service in non-metal-on-metal total joint arthroplasties: A role of metallic particles?

Abstract: Background. The objective of the study was to determine the association between periprosthetic concentrations of selected metals and changes induced in periprosthetic tissues (PT). Methods. PT from 24 patients with metal-on-polyethylene or ceramic-on-polyethylene total joint replacements (TJRs) were examined. Samples underwent histological examination including quantification of cellular populations. Determination of metals was performed according to the published methodology. Results were processed using corr… Show more

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Cited by 4 publications
(6 citation statements)
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References 41 publications
(53 reference statements)
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“…Immunostaining was carried out using a set of specific monoclonal and polyclonal antibodies to identify and visualize different cell types (mast, dendritic cells, histiocytes, including multinucleated giant cells, neutrophils, T lymphocytes, B lymphocytes) as described elsewhere. 28 Immunohistochemistry was performed using an optimized protocol in a Ventana Benchmark XT automated system during the final brown staining of nuclei/cytoplasm and/or membrane of positive cells. All preparations were evaluated by an optical microscope Olympus BX45 (Â20 Â400 magnification, Objective UPLFFLN40X-UIS2, UPlanFLN, Â40/0.75, oo/0.17/FN26.5).…”
Section: Histopathology Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Immunostaining was carried out using a set of specific monoclonal and polyclonal antibodies to identify and visualize different cell types (mast, dendritic cells, histiocytes, including multinucleated giant cells, neutrophils, T lymphocytes, B lymphocytes) as described elsewhere. 28 Immunohistochemistry was performed using an optimized protocol in a Ventana Benchmark XT automated system during the final brown staining of nuclei/cytoplasm and/or membrane of positive cells. All preparations were evaluated by an optical microscope Olympus BX45 (Â20 Â400 magnification, Objective UPLFFLN40X-UIS2, UPlanFLN, Â40/0.75, oo/0.17/FN26.5).…”
Section: Histopathology Methodsmentioning
confidence: 99%
“…Two to three representative blocks were selected from each sample after primary hematoxylin–eosin staining and immunohistochemical methods were applied to prepared consecutive sections with a thickness of 3–4 μm. Immunostaining was carried out using a set of specific monoclonal and polyclonal antibodies to identify and visualize different cell types (mast, dendritic cells, histiocytes, including multinucleated giant cells, neutrophils, T lymphocytes, B lymphocytes) as described elsewhere 28 . Immunohistochemistry was performed using an optimized protocol in a Ventana Benchmark XT automated system during the final brown staining of nuclei/cytoplasm and/or membrane of positive cells.…”
Section: Methodsmentioning
confidence: 99%
“…25 Several studies report on their rare occurrence in the aseptic periprosthetic tissues while their increased numbers are associated with infection. 62,91,92 There is growing evidence that these cells are more versatile and heterogeneous than was previously considered also underlining their new role in chronic inflammation. [93][94][95] Based on these findings, it may be that sustained activity of neutrophils might be beyond at least some clinical manifestations of adverse reaction to TJA and its by-products.…”
Section: How Does Chronic Inflammation Affect Periprosthetic Tissues?mentioning
confidence: 99%
“…The number of lymphocytes increases in the periprosthetic tissues with increasing time of implant service [27]. However, the tissue image analysis cannot differentiate finer, potentially metal-induced tissue changes [28].…”
Section: Histopathology Studiesmentioning
confidence: 99%