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Publicação:
IgG4-positive plasma cells are more often detected in chronic periapical lesions arising from permanent rather than primary teeth

dc.contributor.authorPolanco, X. B.J.
dc.contributor.authorBertasso, A. S.
dc.contributor.authorSilveira, H. A. [UNESP]
dc.contributor.authorYamamoto de Almeida, L. [UNESP]
dc.contributor.authorAlmeida, L. K.Y.
dc.contributor.authorda Silva, R. A.B.
dc.contributor.authorda Silva, L. A.B.
dc.contributor.authorde Rossi, A.
dc.contributor.authorNelson-Filho, P.
dc.contributor.authorLeón, J. E.
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2021-06-25T10:48:58Z
dc.date.available2021-06-25T10:48:58Z
dc.date.issued2021-05-01
dc.description.abstractAim: To characterize plasma cell subsets in chronic periapical lesions affecting permanent and primary teeth. Methodology: Only chronic periapical lesions without root canal treatment were selected. Twenty-one radicular cysts and 7 periapical granulomas affecting permanent teeth and 19 radicular cysts and 4 periapical granulomas affecting primary teeth were assessed for immunoglobulin (Ig) light chain (kappa and lambda), Ig heavy chain (IgG, IgG4, IgA, IgM and IgD) and plasma cell immunohistochemical markers (MUM1/IRF4, EMA and CD138). The data acquired were analysed by Student’s t test, Mann–Whitney U, Friedman test followed by Dunn's multiple comparison test and Spearman’s rank correlation. Results: All cases were polyclonal (having similar kappa/lambda light chain ratios). IgG was most abundant compared to other Ig heavy chains (all, P < 0.001); like Ig light chains, but unlike IgA, there was greater expression of IgG in the primary compared to the permanent dentition, for both radicular cysts (P < 0.001) and periapical granulomas (P = 0.53). Notably, IgG4 expression was greater in the permanent than the primary dentition, for both radicular cyst (P < 0.05) and periapical granuloma (P = 0.65). IgM and IgD expression was scarce and variable, whereas plasma cell populations were detected efficiently through EMA, CD138 and MUM1/IRF4 markers, the latter being more sensitive in both dentitions. Conclusions: There were slight variations in the Ig light and heavy chain profiles in chronic periapical lesions when comparing the permanent and primary dentitions. The ability of IgG4+ plasma cell infiltration to modulate inflammatory responses in chronic periapical lesions arising from permanent as opposed to primary teeth should be considered in future studies.en
dc.description.affiliationDepartment of Pediatric Dentistry Ribeirão Preto Dental School (FORP/USP) University of São Paulo
dc.description.affiliationOral Medicine Department of Diagnosis and Surgery Araraquara Dental School São Paulo State University (UNESP)
dc.description.affiliationOral Pathology Department of Stomatology Public Oral Health and Forensic Dentistry Ribeirão Preto Dental School (FORP/USP) University of São Paulo
dc.description.affiliationUnespOral Medicine Department of Diagnosis and Surgery Araraquara Dental School São Paulo State University (UNESP)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2016/02713-2
dc.description.sponsorshipIdFAPESP: 2016/11419-0
dc.format.extent682-692
dc.identifierhttp://dx.doi.org/10.1111/iej.13464
dc.identifier.citationInternational Endodontic Journal, v. 54, n. 5, p. 682-692, 2021.
dc.identifier.doi10.1111/iej.13464
dc.identifier.issn1365-2591
dc.identifier.issn0143-2885
dc.identifier.scopus2-s2.0-85099094673
dc.identifier.urihttp://hdl.handle.net/11449/207097
dc.language.isoeng
dc.relation.ispartofInternational Endodontic Journal
dc.sourceScopus
dc.subjectdeciduous teeth
dc.subjectIgG4
dc.subjectImmunoglobulin
dc.subjectImmunohistochemistry
dc.subjectperiapical lesion
dc.subjectpermanent teeth
dc.titleIgG4-positive plasma cells are more often detected in chronic periapical lesions arising from permanent rather than primary teethen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.orcid0000-0001-8235-0976[1]
unesp.author.orcid0000-0003-2228-5302[2]
unesp.author.orcid0000-0002-6724-3504[3]
unesp.author.orcid0000-0001-5403-4052[4]
unesp.author.orcid0000-0002-6308-0613[5]
unesp.author.orcid0000-0002-0230-1347[6]
unesp.author.orcid0000-0001-7118-6859[7]
unesp.author.orcid0000-0002-0571-9474[8]
unesp.author.orcid0000-0001-8802-6480[9]
unesp.author.orcid0000-0002-9668-5870[10]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.departmentDiagnóstico e Cirurgia - FOARpt

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