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The Role of Eosinophils in the Regulation of CD4+ T helper 2 Regulated Inflammation

dc.contributor.authorMacKenzie, Jason Rodericken_US
dc.date.accessioned2008-12-07T23:45:00Zen_US
dc.date.accessioned2011-01-04T02:39:31Z
dc.date.available2008-12-07T23:45:00Zen_US
dc.date.available2011-01-04T02:39:31Z
dc.date.created2003-11en_US
dc.date.issued2003en_US
dc.description.abstractThe eosinophil is a leukocyte whose intracellular mediators are considered to play a central role in the pathogenesis of allergic diseases, including allergic asthma, allergic rhinitis and atopic dermatitis, and which is also involved in immunological responses to parasites. Eosinophil differentiation and maturation from bone marrow progenitors is regulated by interleukin-5 (IL-5), which may be secreted by T helper 2 (Th2) T lymphocytes, and is consistently upregulated in allergic conditions. Eotaxin is a potent chemoattractant for circulating and tissue eosinophils, and the production of this chemokine promotes eosinophil infiltration and accumulation within sites of allergic inflammation.¶ ...¶ In conclusion, eosinophils residing in the allergic lung have the capacity to interact with activated T cells, both within this tissue and the draining lymph nodes. Despite their relative inefficiency as antigen presenting cells (Mawhorter et al., 1994), eosinophils may participate en masse in the serial triggering of activated TCRs, and provide appropriate costimulatory signals that modulate T lymphocyte function. Through the elaboration of Th2 cytokines and stimulation of T cell proliferation, antigen presenting eosinophils may transiently prolong or exacerbate the symptoms of allergic diseases. Alternatively, eosinophils presenting relevant antigens may inhibit T cell activity via degranulation, and such activity has recently been observed in a parasite model (Shinkai et al., 2002). Finally, experiments in the OT-II mouse have provided valuable information to suggest that therapies designed to modulate eosinophil numbers in allergic tissues through the secretion of opposing cytokines such as IFN-γ, may be of limited benefit. The results shown here suggest that airways dysfunction remains intact despite significantly reduced pulmonary eosinophiliaen_US
dc.identifier.urihttp://hdl.handle.net/1885/47792en_US
dc.identifier.urihttp://digitalcollections.anu.edu.au/handle/1885/47792
dc.language.isoenen_US
dc.rights.uriThe Australian National Universityen_US
dc.subjectEosinophilen_US
dc.subjectAntigen Presenting Cellen_US
dc.subjectAllergic Airways Diseaseen_US
dc.subjectAADen_US
dc.subjectOvalbuminen_US
dc.subjectOva-transgenicen_US
dc.subjectAsthmaen_US
dc.subjectCD4en_US
dc.subjectLymphocyteen_US
dc.subjectT helper 2en_US
dc.titleThe Role of Eosinophils in the Regulation of CD4+ T helper 2 Regulated Inflammationen_US
dc.typeThesis (PhD)en_US
dcterms.valid2004en_US
local.contributor.affiliationJohn Curtin School of Medical Research, Division of Molecular Bioscienceen_US
local.contributor.affiliationThe Australian National Universityen_US
local.description.refereedyesen_US
local.type.degreeDoctor of Philosophy (PhD)en_US

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