Study of influenza A virus infection in human dendritic cells and epithelial cells.

Influenza A virus (IAV) is an important pathogen which primarily targets epithelial cells of the respiratory tract, but dendritic cells (DCs) residing in the epithelium are also susceptible. DCs play a crucial role in initiating specific adaptive immune response against IAV. In order to determine if...

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Main Author: Noor Faezzah Baharom.
Other Authors: School of Biological Sciences
Format: Final Year Project
Language:English
Published: 2012
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Online Access:http://hdl.handle.net/10356/48618
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-486182023-02-28T18:06:26Z Study of influenza A virus infection in human dendritic cells and epithelial cells. Noor Faezzah Baharom. School of Biological Sciences Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden. Anna Smed Sörensen DRNTU::Science::Biological sciences::Microbiology::Immunology DRNTU::Science::Biological sciences::Microbiology::Virology Influenza A virus (IAV) is an important pathogen which primarily targets epithelial cells of the respiratory tract, but dendritic cells (DCs) residing in the epithelium are also susceptible. DCs play a crucial role in initiating specific adaptive immune response against IAV. In order to determine if IAV replication proceeds differently in DCs and epithelial cells, the susceptibility of these two cell types to IAV, using monocyte-derived DCs (MDDCs) and A549 cell line respectively, was studied. As the maturation status of a DC is critical to its functional performance, the susceptibility of differentially stimulated MDDCs to IAV through activation of different toll-like receptors (TLRs) was also explored. MDDCs supported IAV infection at the expense of cell viability. MDDCs also responded to IAV infection by undergoing maturation. When analysed by flow cytometry, A549 cells exposed to the same dose of IAV were not well infected. Visualization of infection through immunofluorescence staining enabled detection of more infected A549 cells. Maturation of MDDCs via TLR3 and TLR4 partially protected the MDDCs from IAV infection, but not MDDCs matured via TLR7/8. The antiviral activity appears to be dependent on type I interferons (IFNs), as observed through upregulation of IFN-susceptible genes (ISG). Bachelor of Science in Biological Sciences 2012-04-27T07:06:07Z 2012-04-27T07:06:07Z 2011 2011 Final Year Project (FYP) http://hdl.handle.net/10356/48618 en Nanyang Technological University 36 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Science::Biological sciences::Microbiology::Immunology
DRNTU::Science::Biological sciences::Microbiology::Virology
spellingShingle DRNTU::Science::Biological sciences::Microbiology::Immunology
DRNTU::Science::Biological sciences::Microbiology::Virology
Noor Faezzah Baharom.
Study of influenza A virus infection in human dendritic cells and epithelial cells.
description Influenza A virus (IAV) is an important pathogen which primarily targets epithelial cells of the respiratory tract, but dendritic cells (DCs) residing in the epithelium are also susceptible. DCs play a crucial role in initiating specific adaptive immune response against IAV. In order to determine if IAV replication proceeds differently in DCs and epithelial cells, the susceptibility of these two cell types to IAV, using monocyte-derived DCs (MDDCs) and A549 cell line respectively, was studied. As the maturation status of a DC is critical to its functional performance, the susceptibility of differentially stimulated MDDCs to IAV through activation of different toll-like receptors (TLRs) was also explored. MDDCs supported IAV infection at the expense of cell viability. MDDCs also responded to IAV infection by undergoing maturation. When analysed by flow cytometry, A549 cells exposed to the same dose of IAV were not well infected. Visualization of infection through immunofluorescence staining enabled detection of more infected A549 cells. Maturation of MDDCs via TLR3 and TLR4 partially protected the MDDCs from IAV infection, but not MDDCs matured via TLR7/8. The antiviral activity appears to be dependent on type I interferons (IFNs), as observed through upregulation of IFN-susceptible genes (ISG).
author2 School of Biological Sciences
author_facet School of Biological Sciences
Noor Faezzah Baharom.
format Final Year Project
author Noor Faezzah Baharom.
author_sort Noor Faezzah Baharom.
title Study of influenza A virus infection in human dendritic cells and epithelial cells.
title_short Study of influenza A virus infection in human dendritic cells and epithelial cells.
title_full Study of influenza A virus infection in human dendritic cells and epithelial cells.
title_fullStr Study of influenza A virus infection in human dendritic cells and epithelial cells.
title_full_unstemmed Study of influenza A virus infection in human dendritic cells and epithelial cells.
title_sort study of influenza a virus infection in human dendritic cells and epithelial cells.
publishDate 2012
url http://hdl.handle.net/10356/48618
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