{"id":{"repo_id":"cambridge","oai_identifier":"oai:www.repository.cam.ac.uk:1810/366379"},"canonical_url":"https://search.dev.ndltd.org/etd/cambridge/oai:www.repository.cam.ac.uk:1810/366379","repository":{"repo_id":"cambridge","name":"Cambridge University","base_url":"https://api.repository.cam.ac.uk/server/oai/request"},"display":{"title":"The role of natural killer cells in control of varicella zoster virus infection","abstract":"Varicella zoster virus (VZV) is a globally important virus with significant health and economic impacts. Although primary VZV infection is often perceived as a mild childhood illness, VZV infection is lifelong and reactivation of the latent virus in the elderly and immunocompromised population carries significant associated morbidity. Understanding precisely how the body responds to this virus is an important first step in tackling these challenges. As with other components of the innate response, Natural Killer (NK) cells respond directly to VZV infection, and VZV is likely to use evasion strategies to modulate the immune response. This thesis explores the details of this interplay between NK cells and VZV. First, I address the hypothesis that NK cell receptor expression in VZV seropositive patients is different to NK receptor expression in seronegative subjects. By comparing the expression of NK cell receptors in vivo in three cohorts of patients (seronegative, acutely infected, and recovered seropositive) I examine how these findings provide evidence to characterise the NK cell response to VZV, and to provide insight into viral mechanisms to evade detection by NK cells. Secondly, to address the hypothesis that specific ligand-receptor interactions between NK cells and infected cells responsible for control of VZV replication I examine changes in surface expression of NK cell ligands on infected cells in an vitro model of VZV infection using monocyte-derived dendritic cells (MDDC). Finally, using proteomic analysis, I explore changes in expression of proteins in in vitro infection in both monocyte-derived dendritic cells and an immortalised human keratinocytes cell line.","abstract_html":"Varicella zoster virus (VZV) is a globally important virus with significant health and economic impacts. Although primary VZV infection is often perceived as a mild childhood illness, VZV infection is lifelong and reactivation of the latent virus in the elderly and immunocompromised population carries significant associated morbidity. Understanding precisely how the body responds to this virus is an important first step in tackling these challenges. As with other components of the innate response, Natural Killer (NK) cells respond directly to VZV infection, and VZV is likely to use evasion strategies to modulate the immune response. This thesis explores the details of this interplay between NK cells and VZV. First, I address the hypothesis that NK cell receptor expression in VZV seropositive patients is different to NK receptor expression in seronegative subjects. By comparing the expression of NK cell receptors in vivo in three cohorts of patients (seronegative, acutely infected, and recovered seropositive) I examine how these findings provide evidence to characterise the NK cell response to VZV, and to provide insight into viral mechanisms to evade detection by NK cells. Secondly, to address the hypothesis that specific ligand-receptor interactions between NK cells and infected cells responsible for control of VZV replication I examine changes in surface expression of NK cell ligands on infected cells in an vitro model of VZV infection using monocyte-derived dendritic cells (MDDC). Finally, using proteomic analysis, I explore changes in expression of proteins in in vitro infection in both monocyte-derived dendritic cells and an immortalised human keratinocytes cell line.","abstract_has_math":false,"creators":["Allen, Caroline Patricia"],"institution":"University of Cambridge","degree_name":"Doctor of Medicine (MD)","degree_level":"Doctoral","degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":["Ogg, Graham"],"committee_chairs":[],"committee_members":[],"year":2022,"date_issued":"2022-12","date_published":"2022-12","updated_at":"2026-07-24T01:33:28Z","subjects":["Varicella zoster virus (VZV)","Natural Killer (NK) cells","Infection","Immunity","Ligands"],"languages":[],"rights":[],"rights_urls":["https://www.repository.cam.ac.uk/bitstreams/5835641c-09cc-4c9b-9f97-847239418a21/download","https://creativecommons.org/licenses/by-nc-sa/4.0/"],"identifier_entries":[]},"links":{"outbound_url":"https://doi.org/10.17863/CAM.107340","outbound_label":"DOI","outbound_source":"dc:identifier.doi"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Ogg, Graham"]},{"key":"dc:contributor.sponsor","label":"Sponsor","values":["Oxford Health Services Research Fellowship 2012 British Infection Association Research Fellowship 2014"]},{"key":"dc:creator","label":"Author","values":["Allen, Caroline Patricia"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.issued","label":"Date","values":["2022-12"]},{"key":"dc:publisher.institution","label":"Dc Publisher Institution","values":["University of Cambridge"]},{"key":"dc:relation.isreferencedby.uri","label":"Dc Relation Isreferencedby URI","values":["https://www.repository.cam.ac.uk/handle/1810/366379"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]},{"key":"dc:type.qualificationlevel","label":"Dc Type Qualificationlevel","values":["Doctoral"]},{"key":"dc:type.qualificationname","label":"Dc Type Qualificationname","values":["Doctor of Medicine (MD)"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Varicella zoster virus (VZV)","Natural Killer (NK) cells","Infection","Immunity","Ligands"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:rights","label":"Dc Rights","values":["https://www.repository.cam.ac.uk/bitstreams/5835641c-09cc-4c9b-9f97-847239418a21/download","https://creativecommons.org/licenses/by-nc-sa/4.0/"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.doi","label":"DOI","values":["https://doi.org/10.17863/CAM.107340"]},{"key":"dc:identifier.uri","label":"Identifier URI","values":["https://www.repository.cam.ac.uk/bitstreams/28b5f0f6-213e-4d19-9fbb-4ae073934a82/download"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Varicella zoster virus (VZV) is a globally important virus with significant health and economic impacts. 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By comparing the expression of NK cell receptors in vivo in three cohorts of patients (seronegative, acutely infected, and recovered seropositive) I examine how these findings provide evidence to characterise the NK cell response to VZV, and to provide insight into viral mechanisms to evade detection by NK cells. Secondly, to address the hypothesis that specific ligand-receptor interactions between NK cells and infected cells responsible for control of VZV replication I examine changes in surface expression of NK cell ligands on infected cells in an vitro model of VZV infection using monocyte-derived dendritic cells (MDDC). 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By comparing the expression of NK cell receptors in vivo in three cohorts of patients (seronegative, acutely infected, and recovered seropositive) I examine how these findings provide evidence to characterise the NK cell response to VZV, and to provide insight into viral mechanisms to evade detection by NK cells. Secondly, to address the hypothesis that specific ligand-receptor interactions between NK cells and infected cells responsible for control of VZV replication I examine changes in surface expression of NK cell ligands on infected cells in an vitro model of VZV infection using monocyte-derived dendritic cells (MDDC). 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