Ontology highlight
ABSTRACT: Background
Respiratory syncytial virus (RSV) is a poor inducer of antiviral interferon (IFN) responses which result in incomplete immunity and RSV disease. Several RSV proteins alter antiviral responses, including the non-structural proteins (NS1, NS2) and the major viral surface proteins, that is, fusion (F) and attachment (G) proteins. The G protein modifies the host immune response to infection linked in part through a CX3 C chemokine motif. Anti-G protein monoclonal antibodies (mAbs), that is, clones 3D3 and 2D10 that target the G protein CX3C chemokine motif can neutralize RSV and inhibit G protein-CX3CR1 mediated chemotaxis.Objectives
Determine how monoclonal antibodies against the RSV F and G proteins modify the type I and III IFN responses to RSV infection.Desig
SUBMITTER: Bergeron HC
PROVIDER: S-EPMC10017941 | biostudies-literature | 2023 Jan-Dec
REPOSITORIES: biostudies-literature