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dc.contributorWoodard, Craig
dc.contributorHsu, Lilian
dc.contributor.advisorStranford, Sharon
dc.contributor.authorSceats, Lindsay
dc.date.accessioned2011-05-11T13:00:57Z
dc.date.available2011-05-11T13:00:57Z
dc.date.issued2011-05-11
dc.identifier.urihttp://hdl.handle.net/10166/847
dc.description.abstractMurine acquired immunodeficiency syndrome (MAIDS) is a model of immunodeficiency useful for studying human AIDS. Murine leukemia virus (MuLV) produces a fatal disease course in some strains of mice with symptoms mimicking AIDS. BALB/c mice exhibit natural MAIDS resistance and suppress viral replication, while C57BL/6 mice cannot control viral replication and develop MAIDS. Identifying genes and proteins differentially expressed between strains may aid in defining a ‘successful’ immune response against MuLV. Candidate molecules for study include natural immunosuppressors that protect against strong, unnecessary immune responses. Overexpression of immunosuppressors may turn down immune responses necessary for eliminating viruses. Two natural immunosuppressors are indoleamine 2,3-dioxygenase (IDO) and interleukin-10 (IL-10). Immune activators including Type I (α/β) interferons may also be differentially expressed. This study compared the balance in immunosuppressive (IDO and IL-10) versus immune activating (IFN-α/β) molecules between BALB/c and C57BL/6 mice to elucidate relative levels of natural immunosuppression in MAIDS. Techniques used included RNA-based and protein-based assays. No significant differences were seen between strains in IFN-α/β expression, either at the mRNA or protein level. In contrast, results showed significant upregulation of IDO and IL-10 by disease-susceptible mice in the first week of infection. Immunosuppressor upregulation in MAIDS-susceptible mice may prevent effective T cell responses, predisposing susceptible mice towards developing MAIDS. Further study may delineate potential roles for IDO and IL-10 in human development of AIDS.en_US
dc.description.sponsorshipBiological Sciencesen_US
dc.language.isoen_USen_US
dc.subjectImmunologyen_US
dc.titleImmunomodulation in the Murine AIDS Modelen_US
dc.typeThesisen_US
dc.date.gradyear2011en_US
mhc.institutionMount Holyoke College
mhc.degreeUndergraduateen_US
dc.rights.restrictedpublic


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