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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP-
dc.contributor.authorWITKIN, Steven S.-
dc.contributor.authorCHERVENAK, Joseph-
dc.contributor.authorBONGIOVANNI, Ann Marie-
dc.contributor.authorHERWAY, Catherine-
dc.contributor.authorLINHARES, Iara M.-
dc.contributor.authorSKUPSKI, Daniel-
dc.date.accessioned2013-07-30T17:17:29Z-
dc.date.available2013-07-30T17:17:29Z-
dc.date.issued2012-
dc.identifier.citationAMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, v.67, n.1, p.28-33, 2012-
dc.identifier.issn1046-7408-
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/1246-
dc.description.abstractProblem We evaluated the influence of amniotic fluid (AF) on immune mediator production by mononuclear leukocytes. Method of study Thirty mid-gestation AFs were incubated with peripheral blood mononuclear cells (PBMCs) in the presence or absence of lipopolysaccharide (LPS). Supernatants were tested for interleukin (IL) -6, 10, 12, 23, tumor necrosis factor-alpha (TNF-alpha) and monocyte chemotactic protein (MCP)-1. Results Endogenous mediator production was minimal or non-detectable. AF stimulated endogenous MCP-1, IL-6 and TNF-alpha release. In the presence of LPS, production of MCP-1 and IL-10 by PBMCs was enhanced eightto ninefold by AF. Release of IL-6 and IL-23 was enhanced less than twofold by the addition of AF while TNF-alpha production was unchanged. AF-stimulated mediator production was similar irrespective of pregnancy outcome. Conclusion Selective AF stimulation of LPS-mediated MCP-1 and IL-10 release may be a mechanism to promote antibody production and the influx of phagocytic cells to engulf pathogens while downregulating the production of pro-inflammatory cytokines.-
dc.language.isoeng-
dc.publisherWILEY-BLACKWELL-
dc.relation.ispartofAmerican Journal of Reproductive Immunology-
dc.rightsrestrictedAccess-
dc.subjectAmniotic fluid-
dc.subjectcytokines-
dc.subjectimmune regulation-
dc.subjectlipopolysaccharide-
dc.subject.othermonocyte chemotactic protein-1-
dc.subject.otherpregnant rhesus-monkeys-
dc.subject.othernecrosis-factor-alpha-
dc.subject.otherpreterm labor-
dc.subject.othermicrobial invasion-
dc.subject.otheracquired-immunity-
dc.subject.otherinnate-
dc.subject.otherinterleukin-1-beta-
dc.subject.otherinfection-
dc.subject.othercytokine-
dc.titleInfluence of Mid-Trimester Amniotic Fluid on Endogenous and Lipopolysaccharide-Mediated Responses of Mononuclear Lymphoid Cells-
dc.typearticle-
dc.rights.holderCopyright WILEY-BLACKWELL-
dc.identifier.doi10.1111/j.1600-0897.2011.01032.x-
dc.identifier.pmid21682792-
dc.subject.wosImmunology-
dc.subject.wosReproductive Biology-
dc.type.categoryoriginal article-
dc.type.versionpublishedVersion-
hcfmusp.author.externalWITKIN, Steven S.:Cornell Univ, Weill Med Coll, Div Immunol & Infect Dis, Dept Obstet & Gynecol, New York, NY 10065 USA-
hcfmusp.author.externalHERWAY, Catherine:New York Hosp, Queens Med Ctr, Dept Obstet & Gynecol, New York, NY 10021 USA-
hcfmusp.author.externalSKUPSKI, Daniel:New York Hosp, Queens Med Ctr, Dept Obstet & Gynecol, New York, NY 10021 USA-
hcfmusp.description.beginpage28-
hcfmusp.description.endpage33-
hcfmusp.description.issue1-
hcfmusp.description.volume67-
hcfmusp.origemWOS-
hcfmusp.origem.idWOS:000297920700004-
hcfmusp.origem.id2-s2.0-83555173492-
hcfmusp.publisher.cityMALDEN-
hcfmusp.publisher.countryUSA-
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dc.description.indexMEDLINE-
hcfmusp.citation.scopus5-
hcfmusp.scopus.lastupdate2024-04-12-
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LIM/58 - Laboratório de Ginecologia Estrutural e Molecular


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