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dc.contributor.authorCrispim, J. C. O.-
dc.contributor.authorDuarte, R. A.-
dc.contributor.authorSoares, Christiane Pienna-
dc.contributor.authorCosta, R.-
dc.contributor.authorSilva, J. S.-
dc.contributor.authorMendes-Junior, C. T.-
dc.contributor.authorWastowski, I. J.-
dc.contributor.authorFaggioni, L. P.-
dc.contributor.authorSaber, L. T.-
dc.contributor.authorDonadi, E. A.-
dc.date.accessioned2014-05-20T15:33:02Z-
dc.date.accessioned2016-10-25T18:09:28Z-
dc.date.available2014-05-20T15:33:02Z-
dc.date.available2016-10-25T18:09:28Z-
dc.date.issued2008-02-01-
dc.identifierhttp://dx.doi.org/10.1016/j.trim.2007.10.010-
dc.identifier.citationTransplant Immunology. Amsterdam: Elsevier B.V., v. 18, n. 4, p. 361-367, 2008.-
dc.identifier.issn0966-3274-
dc.identifier.urihttp://hdl.handle.net/11449/41781-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/41781-
dc.description.abstractHLA-G is a non-classic Human Leukocyte Antigen (HLA-G) Class I of low polymorphism and restricted tissue distribution that displays tolerogenic functions. In heart transplantation and in combined liver/renal allograft transplantation, the expression of HLA-G has been associated with a lower incidence of acute graft rejection episodes and absence of chronic dysfunction. Since the expression of HLA-G in renal biopsies has been investigated only in few patients who received a combined kidney and liver transplant, in this study we performed a cross-sectional study, systematically comparing the expression of HLA-G in post-transplanted renal grafts, stratifying patients according to the presence or absence of rejection.Patients and Methods: Seventy-three renal specimens (10 with acute rejection and 13 with chronic allograft nephropathy, and 50 with no signs of rejection) were immunohistochemically evaluated for HLA-G expression.Results: In the group as a whole, HLA-G molecules were detected in 40 cases (54.8%). Among specimens that presented HLA-G expression, 2 out of 40 (5%) exhibited acute rejection, 2 (5%) exhibited chronic allograft nephropathy, and the remaining 36 (90%) exhibited no signs of rejection. The comparison between patients with rejection and those without rejection showed that the expression of HLA-G was significantly increased in specimens exhibiting no signs of rejection (p<0.0001). Considering only patients with acute rejection, 8 out of 10 patients showed no HLA-G expression in their kidney biopsies when compared to patients exhibiting no signs of rejection and absence of HLA-G was observed in 14 out of 50 (p=0.0032). Similarly, considering only patients with chronic allograft nephropathy, absence of HLA-G expression was observed in I I out of 13 specimens, whereas in patients without rejection absence of HLA-G was observed in 14 out of 50 (p=0.003). Therapy with tacrolimus was significantly associated with the expression of HLA-G and a better graft prognosis. Conclusions: Our results suggest that HLA-G expression in the kidney allograft and the use of tacrolimus are associated with a lower frequency of acute renal rejection and chronic allograft nephropathy. (c) 2007 Elsevier B.V. All rights reserved.en
dc.format.extent361-367-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectkidney allograften
dc.subjectHLA-Gen
dc.subjectrejectionen
dc.titleHuman leukocyte antigen-G expression after kidney transplantation is associated with a reduced incidence of rejectionen
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)-
dc.description.affiliationUniv São Paulo, Fac Med Ribeirao Preto, Dept Biochem & Immunol, BR-14049900 Ribeirao Preto, SP, Brazil-
dc.description.affiliationUniv São Paulo State, UNESP, Sch Pharmaceut Sci, Dept Clin Anal, São Paulo, Brazil-
dc.description.affiliationUniv São Paulo, FMRP, Div Clin Immunol, São Paulo, Brazil-
dc.description.affiliationUniv São Paulo, FMRP, Dept Pathol, São Paulo, Brazil-
dc.description.affiliationUniversidade Federal de São Carlos (UFSCar), Dept Med, Ctr Biol & Hlth Sci, São Paulo, Brazil-
dc.description.affiliationUniv São Paulo, FMRP, Renal Transplant Unity, São Paulo, Brazil-
dc.description.affiliationUnespUniv São Paulo State, UNESP, Sch Pharmaceut Sci, Dept Clin Anal, São Paulo, Brazil-
dc.identifier.doi10.1016/j.trim.2007.10.010-
dc.identifier.wosWOS:000252572000011-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofTransplant Immunology-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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