Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2592
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dc.contributor.authorSehrawat, S.-
dc.contributor.authorRouse, B.T.-
dc.date.accessioned2020-12-03T09:45:32Z-
dc.date.available2020-12-03T09:45:32Z-
dc.date.issued2017-
dc.identifier.citationFrontiers in Immunology, 8en_US
dc.identifier.other10.3389/fimmu.2017.00341-
dc.identifier.urihttps://www.frontiersin.org/articles/10.3389/fimmu.2017.00341/full-
dc.identifier.urihttp://hdl.handle.net/123456789/2592-
dc.description.abstractIt is now clear that the outcome of an inflammatory process caused by infections depends on the balance of responses by several components of the immune system. Of particular relevance is the interplay between regulatory T cells (Tregs) and CD4+ T cells that produce IL-17 (Th17 cells) during immunoinflammatory events. In addition to discussing studies done in mice to highlight some unresolved issues in the biology of these cells, we emphasize the need to include outbred animals and humans in analyses. Achieving a balance between Treg and Th17 cells responses represents a powerful approach to control events during immunity and immunopathology.en_US
dc.language.isoen_USen_US
dc.publisherFrontiers Research Foundationen_US
dc.subjectAnimalsen_US
dc.subjectCross-regulationen_US
dc.subjectOutbred populationen_US
dc.subjectT regulatory cellsen_US
dc.titleInterplay of regulatory T cell and Th17 cells during infectious diseases in humans and animalsen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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