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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Immunological aspects of fresh-frozen allogeneic bone grafting for lateral ridge augmentation

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Author(s):
Spin-Neto, Rubens [1, 2] ; Stavropoulos, Andreas [3, 4] ; de Freitas, Rubens Moreno [1, 2] ; Violin Dias Pereira, Luis Antonio [5] ; Carlos, Iracilda Zeppone [6] ; Marcantonio, Jr., Elcio [1, 2]
Total Authors: 6
Affiliation:
[1] UNESP Univ Estadual Paulista, Araraquara Dent Sch, Dept Periodontol, Sao Paulo - Brazil
[2] Aarhus Univ, Dept Dent Oral Radiol, DK-8000 Aarhus - Denmark
[3] Aarhus Univ, Dept Dent Periodontol, Sch Dent, DK-8000 Aarhus - Denmark
[4] Ctr Expt & Preclin Biomed Res, Athens - Greece
[5] UNICAMP State Univ Campinas, Dept Histol & Embryol, Inst Biol, Sao Paulo - Brazil
[6] UNESP Univ Estadual Paulista, Araraquara Pharmaceut Sci Sch, Dept Clin Anal, Sao Paulo - Brazil
Total Affiliations: 6
Document type: Journal article
Source: Clinical Oral Implants Research; v. 24, n. 9, p. 963-968, SEP 2013.
Web of Science Citations: 9
Abstract

Objectives: To present some immunological aspects of fresh-frozen allogeneic bone grafting for lateral bone augmentation, based on the quantitative evaluation of IL-10, IL-1 beta, IFN-gamma and TNF-alpha in patients sera. Material and methods: Thirty-three partially or totally edentulous patients received fresh-frozen allogeneic bone (AL - 20 patients) or autologous bone onlay block grafts (AT - 13 patients) prior to oral implant placement. Blood samples were collected from each patient at various time-points during a 6 month-period (baseline, 14, 30, 90 and 180 days postoperatively). Quantitative evaluation of IL-10, IL-1 beta, IFN-gamma and TNF-alpha was performed by enzyme linked immunosorbent assay (ELISA). Results: For all evaluated markers and at all evaluated periods, inter-group comparisons showed no statistically significant differences between the groups, while the observed values were within normal levels. For AL-treated patients, intra-group evaluation showed statistically significant increase of TNF-a from baseline to 90 (P < 0.001) and 180 (P < 0.01) days, and from 14 to 90 (P < 0.01) and 180 (P < 0.05) days. IFN-gamma showed intercalated results, with a decrease from baseline to 14 days (P < 0.05), and increase from 14 to 90 days (P < 0.001) and 180 (P < 0.05) days. No differences between the periods of evaluation were found for the AT group. Conclusions: AL grafting for lateral bone augmentation, similar to AT grafting, does not seem to challenge the immune system significantly. (AU)

FAPESP's process: 08/09207-9 - Bone allografts in humans: immunologic, tomographic, histological and histometrical evaluation of their incorporation and capacity of implants osseointegration
Grantee:Elcio Marcantonio Junior
Support Opportunities: Regular Research Grants