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Identification of Novel Respiratory Syncytial Virus CD4 + and CD8 + T Cell Epitopes in C57BL/6 Mice
Journal article   Open access   Peer reviewed

Identification of Novel Respiratory Syncytial Virus CD4 + and CD8 + T Cell Epitopes in C57BL/6 Mice

Megan E Schmidt and Steven M Varga
ImmunoHorizons, Vol.3(1), pp.1-12
01/14/2019
DOI: 10.4049/immunohorizons.1800056
PMCID: PMC7316092
PMID: 31356172
url
https://doi.org/10.4049/immunohorizons.1800056View
Published (Version of record) Open Access

Abstract

Respiratory syncytial virus (RSV) is the most common cause of lower respiratory tract infection and hospitalization in infants. It is well established that both CD4 and CD8 T cells are critical for mediating viral clearance but also contribute to the induction of immunopathology following RSV infection. C57BL/6 mice are often used to study T cell responses following RSV infection given the wide variety of genetically modified animals available. To date, few RSV-derived CD4 and CD8 T cell epitopes have been identified in C57BL/6 mice. Using an overlapping peptide library spanning the entire RSV proteome, intracellular cytokine staining for IFN-γ was performed to identify novel CD4 and CD8 T cell epitopes in C57BL/6 mice. We identified two novel CD4 T cell epitopes and three novel CD8 T cell epitopes located within multiple RSV proteins. Additionally, we characterized the newly described T cell epitopes by determining their TCR Vβ expression profiles and MHC restriction. Overall, the novel RSV-derived CD4 and CD8 T cell epitopes identified in C57BL/6 mice will aid in future studies of RSV-specific T cell responses.
Animals CD4-Positive T-Lymphocytes - immunology CD8-Positive T-Lymphocytes - immunology Cell Line, Tumor Epitopes, T-Lymphocyte - metabolism Female Histocompatibility Antigens Class I - immunology Interferon-gamma - metabolism Lung - pathology Mice Mice, Inbred C57BL Peptide Library Receptors, Antigen, T-Cell, alpha-beta - metabolism Respiratory Syncytial Virus Infections - pathology Respiratory Syncytial Virus, Human - metabolism Viral Proteins - metabolism

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