Airway Hyperresponsiveness through Synergy of gamma delta T Cells and NKT Cells

Mice sensitized and challenged with OVA were used to investigate the role of innate T cells in the development of allergic airway hyperresponsiveness (AHR). AHR, but not eosinophilic airway inflammation, was induced in T cell-deficient mice by small numbers of cotransferred gamma delta T cells and i...

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Veröffentlicht in:Journal of Immunology 2007-09, Vol.179 (5), p.2961-2968
Hauptverfasser: Jin, Niyun, Miyahara, Nobuaki, Roark, Christina L, French, Jena D, Aydintug, MKemal, Matsuda, Jennifer L, Gapin, Laurent, O'Brien, Rebecca L, Gelfand, Erwin W, Born, Willi K
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Sprache:eng
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Zusammenfassung:Mice sensitized and challenged with OVA were used to investigate the role of innate T cells in the development of allergic airway hyperresponsiveness (AHR). AHR, but not eosinophilic airway inflammation, was induced in T cell-deficient mice by small numbers of cotransferred gamma delta T cells and invariant NKT cells, whereas either cell type alone was not effective. Only V gamma 1 super(+)V delta 5 super(+) gamma delta T cells enhanced AHR. Surprisingly, OVA-specific alpha beta T cells were not required, revealing a pathway of AHR development mediated entirely by innate T cells. The data suggest that lymphocytic synergism, which is key to the Ag-specific adaptive immune response, is also intrinsic to T cell-dependent innate responses.
ISSN:0022-1767
1365-2567
DOI:10.4049/jimmunol.179.5.2961