The activation of pattern recognition receptors (PRRs) is a major regulatory checkpoint for the generation of adaptive immunity. Rig-I-like Receptors (RLRs) are a family of PRRs that recognize microbial RNA in the cytosol and induce proinflammatory cytokines and type I and type III interferons. RLRs are important mediators of innate immunity to multiple viral infections. However, the role of RLRs in the regulation of adaptive immunity is still poorly understood. The adaptive immune response to West Nile Virus (WNV) infection is severely dysregulated in the absence of MAVS (also called IPS-1), the essential signaling adaptor of RLRs. In this proposal, we will elucidate the cellular and molecular mechanisms of the RLR-dependent regulation of B cell responses to WNV. This study will provide fundamental conceptual insights that are necessary for the design of novel vaccines to WNV in particular and RNA viruses in general.

Public Health Relevance

(no more than 3 sentences) The immune system senses infections via specialized receptors that recognize components of the pathogen and orchestrate the ensuing immune response. This project will investigate how such receptors and their signals control the immune response to West-Nile Virus. This work will provide important new insights that are relevant for the design of novel vaccine strategies against West-Nile Virus.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
High Priority, Short Term Project Award (R56)
Project #
1R56AI130044-01A1
Application #
9615353
Study Section
Cellular and Molecular Immunology - A Study Section (CMIA)
Program Officer
Jiang, Chao
Project Start
2018-01-15
Project End
2018-12-31
Budget Start
2018-01-15
Budget End
2018-12-31
Support Year
1
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Arizona
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
806345617
City
Tucson
State
AZ
Country
United States
Zip Code
85721