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dc.contributor.advisorEvans, David
dc.contributor.advisorSandstorm, Kjell
dc.contributor.authorAlam, Fiza
dc.date.accessioned2024-02-22T17:35:36Z
dc.date.available2024-02-22T17:35:36Z
dc.date.issued2023
dc.identifier.urihttp://digital.library.wisc.edu/1793/84965
dc.description.abstractNatural killer (NK) cells are an important part of the immune response and play a vital role in the defense against viral pathogens. NK cell function is characterized by its ability to regulate cytotoxicity and modulate adaptive immunity. NK cell responses are regulated by interaction between highly polymorphic killer-cell immunoglobulin-like receptors (KIR) and major histocompatibility complex (MHC) class I ligands. Non-human primates are a vital model for infectious diseases and NK cell research. However, this research is limited by a lack of defined ligands. In this project, I tested the ligand binding of polymorphic KIR alleles against a panel of Mamu-A and Mamu-B ligands using JNL assays. This will give insight into defining functional differences between allotypes and what may cause these differences.en_US
dc.language.isoenen_US
dc.rightsThe author hereby grants to University of Wisconsin-Madison the permission to reproduce and to distribute publicly paper and electronic copies of this thesis document in whole or in part in any medium now known or hereafter created.en_US
dc.titleInvestigating the Binding Specificity of Polymorphic KIR Alleles with Potential Ligandsen_US
dc.typeThesisen_US


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