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dc.date.accessioned 2022-05-23T13:02:50Z
dc.date.available 2022-05-23T13:02:50Z
dc.date.issued 2009-08
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/136688
dc.description.abstract Based on a unifying theory presented here, it is predicted that the immune defects resulting in chronic inflammation rather than effective immune responses could be rectified by the therapeutic use of agents prepared from micro-organisms. With appropriate molecular patterns, these should be able to induce protective immunoregulatory networks or to reprogramme defective ones. In contrast to acute inflammation, chronic inflammation appears to have no beneficial role, but is a state of sustained immune reactivity in the presence or progression of a disease process. This results in an escalating cycle of tissue damage followed by unproductive tissue repair, breaks in self-tolerance, malignant transformation or deleterious changes in tissue morphology and function. Such inappropriate immune reactivity is an underlying characteristic, either in initiation or maintenance, of a diverse range of disease states including chronic infection, autoimmunity, allergy, cancer, vascular disease and metabolic alterations. Evidence is presented that the inappropriate immune reactivity is due, at least to some extent, to failures in the establishment of immunoregulatory networks as a result of hygiene-related factors. Such networks are the result of activation of antigen-presenting cells, principally dendritic cells, by molecular patterns of micro-organisms encountered sequentially during life and establishing the ‘biography’ of the immune system. en
dc.format.extent 193-203 es
dc.language en es
dc.subject Inflammation es
dc.subject Infection es
dc.subject Immune regulation es
dc.subject Immunopathology es
dc.subject Autoimmunity es
dc.subject Cancer es
dc.subject Metabolism es
dc.subject Hygiene hypothesis es
dc.title Chronic inflammation as a manifestation of defects in immunoregulatory networks: implications for novel therapies based on microbial products en
dc.type Articulo es
sedici.identifier.other doi:10.1007/s10787-009-0008-x es
sedici.identifier.other pmid:19597940 es
sedici.identifier.issn 1568-5608 es
sedici.identifier.issn 0925-4692 es
sedici.creator.person Bottasso, Oscar es
sedici.creator.person Docena, Guillermo Horacio es
sedici.creator.person Stanford, John Lawson es
sedici.creator.person Grange, J. M. es
sedici.subject.materias Ciencias Exactas es
sedici.subject.materias Medicina es
sedici.description.fulltext true es
mods.originInfo.place Laboratorio de Investigaciones del Sistema Inmune es
sedici.subtype Articulo es
sedici.rights.license Creative Commons Attribution 4.0 International (CC BY 4.0)
sedici.rights.uri http://creativecommons.org/licenses/by/4.0/
sedici.description.peerReview peer-review es
sedici.relation.journalTitle Inflammopharmacology es
sedici.relation.journalVolumeAndIssue vol. 17, no. 4 es


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Creative Commons Attribution 4.0 International (CC BY 4.0) Excepto donde se diga explícitamente, este item se publica bajo la siguiente licencia Creative Commons Attribution 4.0 International (CC BY 4.0)