Dendritic cell NLRC4 regulates influenza A virus–specific CD4+ T cell responses through FasL expression
Year: 2019
Type: article
Abstract: Influenza A virus (IAV)-specific T cell responses are important correlates of protection during primary and subsequent infections. Generation and maintenance of robust IAV-specific T cell responses relies on T cell interactions with dendritic cells (DCs). In this study, we explore the role of nucleotide-binding domain leucine-rich repeat containing receptor family member NLRC4 in modulating the DC phenotype during IAV infection. Nlrc4-/- mice had worsened survival and increased viral titers during infection, normal innate immune cell recruitment and IAV-specific CD8 T cell responses, but severely blunted IAV-specific CD4 T cell responses compared to wild-type mice. The defect in the pulmonary IAV-specific CD4 T cell response was not a result of defective priming or migration of these cells in Nlrc4-/- mice but was instead due to an increase in FasL+ DCs, resulting in IAV-specific CD4 T cell death. Together, our data support a novel role for NLRC4 in regulating the phenotype of lung DCs during a respiratory viral infection, and thereby influencing the magnitude of protective T cell responses.
DOI: 10.1172/jci124937
Language: English
Subfield: Epidemiology
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
Funders: Harry J. Lloyd Charitable Trust, Cedars-Sinai Medical Center, National Institutes of Health, Holden Comprehensive Cancer Center, University of Iowa, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, National Heart, Lung, and Blood Institute, National Institute of Allergy and Infectious Diseases
OpenAlex ID: W2943439696
