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B and T Lymphocyte Attenuator Regulates T Cell Survival in the Lung
Author(s) -
Christine Deppong,
Jessica M. Degnan,
Theresa L. Murphy,
Kenneth M. Murphy,
Jonathan M. Green
Publication year - 2008
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.181.5.2973
Subject(s) - btla , immunology , attenuator (electronics) , receptor , lymphocyte , t lymphocyte , inflammation , t cell , medicine , biology , immune system , physics , attenuation , optics
The initiation, intensity, and duration of T cell-directed inflammatory responses are dependent upon the coordination of both activating and inhibitory signals mediated by specific receptors on the T lymphocyte. The recently described receptor, B and T lymphocyte attenuator (BTLA), has been demonstrated to have an important role in limiting the duration of inflammation in a murine model of allergic asthma. In this study, we have examined the role of BTLA on the proliferation, recruitment, and survival of T cells in response to inhaled allergen. We find that there is decreased cell death in T cells from BTLA-deficient mice, whereas proliferation and recruitment to the lungs are unchanged. Thus, the regulation of cell death through BTLA signaling is a key determinant of the inflammatory response in the lung.

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