Bacterial lipopolysaccharide inhibits influenza virus infection of human macrophages and the consequent induction of CD8+ T cell immunity

Autor: Short, Kirsty R, Vissers, Marloes, de Kleijn, Stan, Zomer, Aldert L, Kedzierska, Katherine, Grant, Emma, Reading, Patrick C, Hermans, Peter W M, Ferwerda, Gerben, Diavatopoulos, Dimitri A, LS Klinisch Onderzoek Wagenaar
Přispěvatelé: LS Klinisch Onderzoek Wagenaar
Jazyk: angličtina
Rok vydání: 2014
Předmět:
Lipopolysaccharides
Antigen presentation
lnfectious Diseases and Global Health Radboud Institute for Molecular Life Sciences [Radboudumc 4]
Other Research Radboud Institute for Molecular Life Sciences [Radboudumc 0]
Biology
CD8-Positive T-Lymphocytes
Virus Replication
Virus
Microbiology
Madin Darby Canine Kidney Cells
03 medical and health sciences
Interferon-gamma
Immune system
Dogs
Antigen
Interferon
medicine
Immunology and Allergy
Cytotoxic T cell
Animals
Humans
Cells
Cultured

030304 developmental biology
Oligonucleotide Array Sequence Analysis
0303 health sciences
Antigen Presentation
Bacterial disease
030306 microbiology
Reverse Transcriptase Polymerase Chain Reaction
Tumor Necrosis Factor-alpha
Macrophages
Interferon-beta
Acquired immune system
Flow Cytometry
Coculture Techniques
3. Good health
Influenza A virus
Immunology
Host-Pathogen Interactions
Transcriptome
medicine.drug
HeLa Cells
Research Article
Zdroj: Journal of Innate Immunity, 6(2), 129. S. Karger AG
Journal of Innate Immunity, 6, 2, pp. 129-39
Journal of Innate Immunity, 6, 129-39
ISSN: 1662-811X
Popis: Contains fulltext : 127685.pdf (Publisher’s version ) (Open Access) It is well established that infection with influenza A virus (IAV) facilitates secondary bacterial disease. However, there is a growing body of evidence that the microbial context in which IAV infection occurs can affect both innate and adaptive responses to the virus. To date, these studies have been restricted to murine models of disease and the relevance of these findings in primary human cells remains to be elucidated. Here, we show that pre-stimulation of primary human monocyte-derived macrophages (MDMs) with the bacterial ligand lipopolysaccharide (LPS) reduces the ability of IAV to infect these cells. The inhibition of IAV infection was associated with a reduced transcription of viral RNA and the ability of LPS to induce an anti-viral/type I interferon response in human MDMs. We demonstrated that this reduced rate of viral infection is associated with a reduced ability to present a model antigen to autologous CD8+ T cells. Taken together, these data provide the first evidence that exposure to bacterial ligands like LPS can play an important role in modulating the immune response of primary human immune cells towards IAV infection, which may then have important consequences for the development of the host's adaptive immune response.
Databáze: OpenAIRE