DESCRIPTION (provided by applicant): West Nile virus (WNV) is a neurotropic flavivirus that is the leading cause of arboviral encephalitis in the United States. The need to study WNV pathogenesis and the host immune response to infection is imperative as there are no specific therapies or vaccines available for human use. The search for effective intervention strategies relies on a better basic science understanding of the pathogenesis of WNV. Inflammatory monocytes are critical mediators of the antiviral response against WNV and accumulate in the CNS during WNV encephalitis. In preliminary data, we show that efficient accumulation of monocytes in the CNS first requires the release of monocyte from the bone marrow, a step that is entirely dependent on chemokine receptor CCR2. In this application, we will evaluate the relative contribution of the CCR2 ligands, chemokines CCL2 and CCL7, in mediating this monocytosis during WNV infection (Aim 1), and evaluate the extent to which these ligands, given exogenously, can promote monocyte accumulation in the CNS and alter the outcome of infection (Aim 2). Since monocytes appear to play a protective role within the CNS, understanding the chemokines that regulate their release from the bone marrow, and the potential to exploit this step to modulate monocyte accumulation in the CNS, is an important goal with translational implications.
|Effective start/end date||17/01/14 → 16/01/16|
- National Institute of Allergy and Infectious Diseases: $36,792.00
- National Institute of Allergy and Infectious Diseases: $35,892.00
- National Institute of Allergy and Infectious Diseases: $36,336.00
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