dc.creatorStojanova, Jana
dc.creatorPouche, Lucie
dc.creatorPicard, Nicolas
dc.date.accessioned2016-06-28T22:40:27Z
dc.date.available2016-06-28T22:40:27Z
dc.date.created2016-06-28T22:40:27Z
dc.date.issued2016
dc.identifierClinical Biochemistry 49 (2016) 363–376
dc.identifierDOI: 10.1016/j.clinbiochem.2015.07.016
dc.identifierhttps://repositorio.uchile.cl/handle/2250/139250
dc.description.abstractThe modulation of the immune system following solid organ transplantation has made considerable progress with new immunosuppressive regimens and has considerably improved rejections rates. The improvement in long-term allograft survival is, however, modest. A complex network of cytokines, chemokines, adhesion, activation and co-stimulatory molecules are the frontline contributors to allograft rejection, which in turn determines the evolution of graft function and its long-term survival. Polymorphisms in these genes influence protein levels and presumably their signaling effects. In this review, we present a relevant panel of candidate genes related to the immune system in the context of solid organ transplantation; we discuss the most convincing reports of genetic associations with outcomes in renal transplantation and highlight the most promising loci among the vast body of literature.
dc.languageen
dc.publisherElsevier
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 Chile
dc.subjectTransplantation
dc.subjectImmune response
dc.subjectImmunosuppressive therapy
dc.subjectCytokines
dc.subjectGene polymorphism
dc.titleGenetic polymorphisms in the immune response: A focus on kidney transplantation
dc.typeArtículo de revista


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