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J Allergy Clin Immunol ; 129(1): 191-8.e1-4, 2012 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-22079492

RESUMEN

BACKGROUND: IL-4, IL-5, and IL-13 are thought to be central to the allergic asthmatic response. Previous work supposed that the essential source of these cytokines was CD4(+) T(H)2 cells. However, more recent studies have suggested that other innate production of type 2 cytokines might be as important. OBJECTIVES: Nuocytes are a novel population of IL-13-producing innate cells, which are critical for protective immunity in Nippostrongylus brasiliensis infection. Given this, we investigated the potential existence and functional importance of nuocytes in experimental allergic asthma. METHODS: We generated Il4(+/eGFP)Il13(+/Tomato) dual-reporter mice to study cytokine-producing cells during allergic inflammation. We adoptively transferred innate IL-13-producing cells to investigate their role in airways hyperreactivity (AHR). RESULTS: We show that allergen-induced nuocytes infiltrate the lung and are a major innate source of IL-13. CD4(+) T cells in the lung almost exclusively express only IL-13, whereas IL-4-producing T cells were restricted to the draining lymph nodes. Intranasal administration of IL-25 or IL-33 induced IL-13-producing nuocytes in the BAL fluid. Strikingly, adoptive transfer of wild-type nuocytes, but not Il13(-/-) nuocytes, into Il13(-/-) mice, which are normally resistant to IL-25-induced AHR, restored airways resistance and lung cell infiltration. CONCLUSIONS: These findings identify nuocytes as a novel cell type in allergic lung inflammation and an innate source of IL-13 that can directly induce AHR in the absence of IL-13-producing CD4(+) T cells. These data highlight nuocytes as an important new consideration in the development of future allergic asthma therapy.


Asunto(s)
Asma/inmunología , Hiperreactividad Bronquial/inmunología , Inmunidad Innata , Interleucina-13/biosíntesis , Neumonía/inmunología , Administración Intranasal , Animales , Asma/genética , Asma/metabolismo , Hiperreactividad Bronquial/genética , Hiperreactividad Bronquial/metabolismo , Citocinas/administración & dosificación , Citocinas/genética , Citocinas/inmunología , Modelos Animales de Enfermedad , Ratones , Ratones Endogámicos BALB C , Ratones Transgénicos , Neumonía/genética , Neumonía/metabolismo
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