Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/29574
Full metadata record
DC FieldValueLanguage
dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP-
dc.contributor.authorLIRA, Aline Aparecida de Lima-
dc.contributor.authorDE-OLIVEIRA, Marilia Garcia-
dc.contributor.authorINOUE, Amanda Harumi Sabo-
dc.contributor.authorBELTRAME, Giovanna Rossi-
dc.contributor.authorDUARTE, Alberto Jose da Silva-
dc.contributor.authorVICTOR, Jefferson Russo-
dc.date.accessioned2018-11-21T17:06:23Z-
dc.date.available2018-11-21T17:06:23Z-
dc.date.issued2018-
dc.identifier.citationALLERGOLOGIA ET IMMUNOPATHOLOGIA, v.46, n.5, p.454-459, 2018-
dc.identifier.issn0301-0546-
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/29574-
dc.description.abstractBackground: IL-17-producing B cells can be identified in both mice and human and were named B17 cells. The role of B17 cells still needs to be elucidated and its inflammatory or regulatory functions remain controversial. Objective: We evaluate the effect of maternal immunization with OVA on offspring B cells that produces IL-17 and can show a regulatory potential by IL-10 production. Methods: C57BL/6 WT, IL-10(-/-) or CD28(-/-) female mice were immunized or not with OVA in Alum, and immunized females were boosted after 10 and 20 days. Immunized and non immunized females were mated, and pups from both groups were evaluated at 3 or 20 days old (d.o.). Some offspring from the aforementioned two groups were immunized with OVA at 3 d.o., boosted after 10 days and evaluated at 20 d.o. Results: Maternal immunization with OVA induced offspring B cells to produce IL-17 at higher intensity compared to the control group of offspring at 3 d.o. This effect was maintained until 20 d.o. and even after neonatal immunization with OVA. The co-production of IL-10 on offspring IL-17 + B cells is up-regulated in response to maternal immunization with OVA. Maternal immunization with OVA on IL-10(-/-)mice reveals reduced percentage and mean of fluorescence intensity of IL-17 on B cells of offspring. Conclusion: Preconception OVA immunization can induce offspring B cells that produce IL-17 at higher intensity and co-produce mainly IL-10. This could be the reason why B17 cells had been described in the literature with controversial roles upon their regulatory function.-
dc.description.sponsorshipSao Paulo Research Foundation (FAPESP) [2015/17256-3, 2017/18558-9, 2013/22820-0]-
dc.description.sponsorshipNational Council for Scientific and Technological Development (CNPq) [115603/2015-8]-
dc.language.isoeng-
dc.publisherELSEVIER DOYMA SL-
dc.relation.ispartofAllergologia et Immunopathologia-
dc.rightsrestrictedAccess-
dc.subjectAllergy-
dc.subjectOVA-
dc.subjectMaternal-fetal interface-
dc.subjectIL-17-
dc.subjectB cells-
dc.subject.otheri hypersensitivity response-
dc.subject.othermaternal immunization-
dc.subject.othert-cells-
dc.subject.othermice-
dc.subject.othersensitization-
dc.subject.othertolerance-
dc.subject.otherexposure-
dc.subject.otheranergy-
dc.titlePreconceptional allergen immunization can induce offspring IL-17 secreting B cells (B17): do they share similarities with regulatory B10 cells?-
dc.typearticle-
dc.rights.holderCopyright ELSEVIER DOYMA SL-
dc.identifier.doi10.1016/j.aller.2018.04.001-
dc.identifier.pmid30082063
dc.subject.wosAllergy-
dc.subject.wosImmunology-
dc.type.categoryoriginal article-
dc.type.versionpublishedVersion-
hcfmusp.author.externalDE-OLIVEIRA, Marilia Garcia:Univ Sao Paulo, Med Sch, Div Clin Dermatol, Lab Med Invest LIM 56, Sao Paulo, Brazil-
hcfmusp.author.externalBELTRAME, Giovanna Rossi:Univ Sao Paulo, Med Sch, Div Clin Dermatol, Lab Med Invest LIM 56, Sao Paulo, Brazil-
hcfmusp.description.beginpage454-
hcfmusp.description.endpage459-
hcfmusp.description.issue5-
hcfmusp.description.volume46-
hcfmusp.origemWOS-
hcfmusp.origem.idWOS:000442841300007-
hcfmusp.origem.id2-s2.0-85049485519-
hcfmusp.publisher.cityBARCELONA-
hcfmusp.publisher.countrySPAIN-
hcfmusp.relation.referenceBento-de-Souza Luciana, 2016, Results Immunol, V6, P15, DOI 10.1016/j.rinim.2016.04.001-
hcfmusp.relation.referenceBermejo DA, 2013, NAT IMMUNOL, V14, P514, DOI 10.1038/ni.2569-
hcfmusp.relation.referenceCarter NA, 2012, ARTHRITIS RES THER, V14, DOI 10.1186/ar3736-
hcfmusp.relation.referenceCarter NA, 2011, J IMMUNOL, V186, P5569, DOI 10.4049/jimmunol.1100284-
hcfmusp.relation.referenceLira AAD, 2014, ALLERGY ASTHMA CL IM, V10, DOI 10.1186/1710-1492-10-47-
hcfmusp.relation.referencede Oliveira MG, 2017, ALLERGY ASTHMA CL IM, V13, P1563-
hcfmusp.relation.referenceFreer G, 2013, METHODS, V61, P30, DOI 10.1016/j.ymeth.2013.03.035-
hcfmusp.relation.referenceFusaro AE, 2002, INT ARCH ALLERGY IMM, V127, P208, DOI 10.1159/000053865-
hcfmusp.relation.referenceFusaro AE, 2007, IMMUNOLOGY, V122, P107, DOI 10.1111/j.1365-2567.2007.02618.x-
hcfmusp.relation.referenceFusaro AE, 2009, IMMUNOLOGY, V128, pe541, DOI 10.1111/j.1365-2567.2008.03028.x-
hcfmusp.relation.referenceFutata EA, 2006, IMMUNOBIOLOGY, V211, P157, DOI 10.1016/j.imbio.2005.08.006-
hcfmusp.relation.referenceMavropoulos A, 2017, CLIN IMMUNOL, V184, P26, DOI 10.1016/j.clim.2017.04.013-
hcfmusp.relation.referenceMavropoulos A, 2017, CLIN IMMUNOL, V184, P33, DOI 10.1016/j.clim.2017.04.010-
hcfmusp.relation.referenceMuniz BP, 2014, IMMUNOBIOLOGY, V219, P377, DOI 10.1016/j.imbio.2014.01.002-
hcfmusp.relation.referenceNoh Joonyong, 2012, Inflammation & Allergy Drug Targets, V11, P320-
hcfmusp.relation.referenceOliveira CR, 2005, J CLIN IMMUNOL, V25, P153, DOI 10.1007/s10875-005-2821-3-
hcfmusp.relation.referencePan W, 2017, PARASITE VECTOR, V10, DOI 10.1186/s13071-017-2263-9-
hcfmusp.relation.referenceRigato PO, 2009, IMMUNOTHERAPY, V1, P141, DOI 10.2217/1750-743X.1.1.141-
hcfmusp.relation.referenceSchlegel PM, 2013, PLOS ONE, V8, DOI 10.1371/journal.pone.0082580-
hcfmusp.relation.referenceSgnotto FDR, 2017, HUM VACCIN IMMUNOTHE, V13-
hcfmusp.relation.referenceVictor JR, 2010, BMC IMMUNOL, V11, DOI 10.1186/1471-2172-11-11-
hcfmusp.relation.referenceVictor JR, 2017, HUM VACC IMMUNOTHER, V13, P507, DOI 10.1080/21645515.2016.1244592-
hcfmusp.relation.referenceVictor JR, 2014, J IMMUNOL RES, DOI 10.1155/2014/780386-
hcfmusp.relation.referenceVictor JR, 2003, J ALLERGY CLIN IMMUN, V111, P269, DOI 10.1067/mai.2003.39-
dc.description.indexMEDLINE-
dc.identifier.eissn1578-1267-
hcfmusp.citation.scopus8-
hcfmusp.scopus.lastupdate2022-05-06-
Appears in Collections:

Artigos e Materiais de Revistas Científicas - FM/MPT
Departamento de Patologia - FM/MPT

Artigos e Materiais de Revistas Científicas - HC/ICHC
Instituto Central - HC/ICHC

Artigos e Materiais de Revistas Científicas - LIM/56
LIM/56 - Laboratório de Investigação em Dermatologia e Imunodeficiências


Files in This Item:
File Description SizeFormat 
art_LIRA_Preconceptional_allergen_immunization_can_induce_offspring_IL17_secreting_2018.PDF
  Restricted Access
publishedVersion (English)718.29 kBAdobe PDFView/Open Request a copy

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.