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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/76444
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dc.contributor.authorSpin-Neto, Rubens-
dc.contributor.authorStavropoulos, Andreas-
dc.contributor.authorDe Freitas, Rubens Moreno-
dc.contributor.authorPereira, Luís Antônio Violin Dias-
dc.contributor.authorCarlos, Iracilda Zeppone-
dc.contributor.authorMarcantonio, Elcio-
dc.date.accessioned2014-05-27T11:30:33Z-
dc.date.accessioned2016-10-25T18:53:35Z-
dc.date.available2014-05-27T11:30:33Z-
dc.date.available2016-10-25T18:53:35Z-
dc.date.issued2013-09-01-
dc.identifierhttp://dx.doi.org/10.1111/j.1600-0501.2012.02510.x-
dc.identifier.citationClinical Oral Implants Research, v. 24, n. 9, p. 963-968, 2013.-
dc.identifier.issn0905-7161-
dc.identifier.issn1600-0501-
dc.identifier.urihttp://hdl.handle.net/11449/76444-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/76444-
dc.description.abstractObjectives: To present some immunological aspects of fresh-frozen allogeneic bone grafting for lateral bone augmentation, based on the quantitative evaluation of IL-10, IL-1β, IFN- γ and TNF- α 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-1β, IFN- γ and TNF- α 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-α 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- γ 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. © 2012 John Wiley & Sons A/S.en
dc.format.extent963-968-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectBone allograft-
dc.subjectBone autograft-
dc.subjectELISA-
dc.subjectImmunological evaluation-
dc.subjectRidge augmentation-
dc.titleImmunological aspects of fresh-frozen allogeneic bone grafting for lateral ridge augmentationen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionAarhus University (AU)-
dc.contributor.institutionCenter for Experimental and Preclinical Biomedical Research (CEPBR)-
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)-
dc.description.affiliationDepartment of Periodontology UNESP - Univ. Estadual Paulista Araraquara Dental School, Araraquara, São Paulo-
dc.description.affiliationDepartment of Dentistry - Oral Radiology Aarhus University, Aarhus-
dc.description.affiliationDepartment of Dentistry - Periodontology School of Dentistry Aarhus University, Aarhus-
dc.description.affiliationCenter for Experimental and Preclinical Biomedical Research (CEPBR), Athens-
dc.description.affiliationDepartment of Histology and Embryology UNICAMP - State University of Campinas Institute of Biology, Campinas, São Paulo-
dc.description.affiliationDepartment of Clinical Analysis UNESP - Univ. Estadual Paulista Araraquara Pharmaceutical Sciences School, Araraquara, São Paulo-
dc.description.affiliationUnespDepartment of Periodontology UNESP - Univ. Estadual Paulista Araraquara Dental School, Araraquara, São Paulo-
dc.description.affiliationUnespDepartment of Clinical Analysis UNESP - Univ. Estadual Paulista Araraquara Pharmaceutical Sciences School, Araraquara, São Paulo-
dc.identifier.doi10.1111/j.1600-0501.2012.02510.x-
dc.identifier.wosWOS:000322203500002-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofClinical Oral Implants Research-
dc.identifier.scopus2-s2.0-84880821871-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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