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dc.contributor.authorVillegas Martínez, Enrique
dc.contributor.authorSantiago, O.
dc.contributor.authorSolorzano Puerto, Antonio
dc.contributor.authorGutiérrez Fernández, José 
dc.date.accessioned2024-03-22T08:22:33Z
dc.date.available2024-03-22T08:22:33Z
dc.date.issued2010-09
dc.identifier.citationVillegas E, Santiago O, Sorlózano A, Gutierrez J. New strategies and patent therapeutics in EBV-associated diseases. Mini Rev Med Chem. 2010 Sep;10(10):914-27.es_ES
dc.identifier.urihttps://hdl.handle.net/10481/90178
dc.description.abstractEpstein-Barr virus (EBV) is a virus present all throughout the world that causes infectious mononucleosis (IM) and is highly associated with certain malignancies. This study is a review of current knowledge concerning the pathogenic mechanisms of EBV in tumor and auto-immune diseases and the different new strategies to treat EBV associated pathologies. Phenomena surrounding the proliferation and immortalization of B lymphocytes, the mechanisms of immune escape and the role of CD8+ and CD4+ T cells in the infection by EBV are explained. An analysis is made of the role of EBV proteins during the biological events that take place in primary infection, persistent chronic infection together with an update of the approaches of novel patented therapeutics. Currently there is no vaccine protecting against EBV-associated disorders and no treatment that may inhibit or eliminate their progression. Thus, it is crucial to obtain additional information on the function and importance of genes that play a role on the development of those diseases with which it is associated, as well as on the humoral and cellular immune processes involved in them.es_ES
dc.language.isoenges_ES
dc.publisherMini Rev Med Chem .es_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleNew strategies and patent therapeutics in EBV-associated diseaseses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.doi10.2174/138955710792007150


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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