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dc.creatorIzquierdo Álvarez, Elena-
dc.creatorBarber Hernández, Domingo-
dc.creatorVillaseñor Solis, Alma Cristina-
dc.date2021-
dc.date.accessioned2021-09-16T04:00:13Z-
dc.date.available2021-09-16T04:00:13Z-
dc.date.issued2021-09-16-
dc.identifier000000723591-
dc.identifier.urihttp://hdl.handle.net/10637/13009-
dc.descriptionArtículo en colaboración con: A. Villaseñor, E. Izquierdo, M. Huang, T.C. Barker-Tejeda, U. Radzikowska, M. Sokolowska, D. Barber-
dc.descriptionEn: Frontiers in Immunology. e-ISSN 1664-3224 2021,Jul 28,12:692004-
dc.description.abstractThere is increasing evidence that the metabolic status of T cells and macrophages is associated with severe phenotypes of chronic inflammation, including allergic inflammation. Metabolic changes in immune cells have a crucial role in their inflammatory or regulatory responses. This notion is reinforced by metabolic diseases influencing global energy metabolism, such as diabetes or obesity, which are known risk factors of severity in inflammatory conditions, due to the metabolic-associated inflammation present in these patients. Since several metabolic pathways are closely tied to T cell and macrophage differentiation, a better understanding of metabolic alterations in immune disorders could helpto restore andmodulate immune cell functions. This link between energy metabolism and inflammation can be studied employing animal, human or cellular models. Analytical approaches rank from classic immunological studies to integrated analysis of metabolomics, transcriptomics, and proteomics. This review summarizes the main metabolic pathways of the cells involved in the allergic reaction with a focus on T cells and macrophages and describes different models and platforms of analysis used to study the immune system and its relationship with metabolism.en-EN
dc.formatapplication/pdf-
dc.language.isoen-
dc.relationThis work was supported by Instituto de Salud Carlos III (project numbers PI19/00044 and PI18/01467) co-funded by European Regional Development Fund “Investing in your future” for the thematic network and co-operative research centers ARADyAL RD16/0006/0015 and by the Swiss National Science Foundation (SNF) grant nr 310030_189334 (to MS lab), and GlaxoSmithKline (GSK) scientific research grant (to MS lab). JR-C was supported by FPI-CEU predoctoral fellowship and a SEMP fellowship from University of Zurich. TB-T was supported by FPI-CEU predoctoral fellowship. AV is funded by a postdoctoral research fellowship from ARADyAL. MH and UR were supported by the SNF, GSK and SIAF.en-EN
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.es-
dc.subjectAllergyen-EN
dc.subjectImmunometabolismen-EN
dc.subjectImmune cellsen-EN
dc.subjectMetabolic regulationen-EN
dc.subjectOmicsen-EN
dc.titleThe Importance of Metabolism for Immune Homeostasis in Allergic Diseases.en-EN
dc.typeArtículo-
dc.centroUniversidad San Pablo-CEU-
Aparece en las colecciones: Facultad de Farmacia




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