Show simple item record

dc.contributor.authorKrige, Lindel
dc.date.accessioned2014-03-04T18:28:29Z
dc.date.available2014-03-04T18:28:29Z
dc.date.issued2010-05
dc.identifier.otherkrige_lindel_201005_bs
dc.identifier.urihttp://purl.galileo.usg.edu/uga_etd/krige_lindel_201005_bs
dc.identifier.urihttp://hdl.handle.net/10724/26379
dc.description.abstractPregnant women and children are most vulnerable to malarial infection. Malaria in pregnancy leads to intrauterine growth restriction and preterm deliveries, resulting in low birth weight babies. The underlying mechanisms that lead to these poor birth outcomes are not well understood, but it is known that severe inflammation in the placenta together with excessive fibrin deposition are common features of placental malaria, and correlate with low birth weight. These inflammation and coagulation processes in the placenta occur as an immunological response to the malaria infection. This study addresses the hypothesis that local malaria-induced inflammatory responses induce placental coagulopathy, which is turn leads to significant compromise in placental function, and therefore, fetal distress. This study will mainly focus on the role of coagulation and immunological factors in the disease response process of mice. Murine placental malaria has proven to be an effective model for P. falciparum infection in humans. Mouse RNA has been isolated, and primers for each coagulation factor have been developed. Using these primers and isolated RNA, the next step will be to conduct real time PCR to determine possible upregulation of the coagulation factors. Further research possibilities include determining whether fetal or maternal cells initiate this immunological response leading to inflammation and coagulation in the placenta. Identifying the role of coagulation factors involved in the immunological response to placental malaria will provide further understanding on malarial pathogenesis and ways to prevent fetal growth restriction.
dc.languageeng
dc.publisheruga
dc.rightspublic
dc.subjectPlacental Malaria
dc.subjectCoagulation
dc.subjectMouse Model
dc.subjectTissue Factor
dc.subjectTissue Factor Pathway Inhibitor
dc.subjectPlasminogen Activator Inhibitor
dc.subjectThrombomodulin
dc.subjectProtease Activated Receptors
dc.titleCoagulation factors involved in the pathology of placental malaria
dc.typeHonors
dc.description.degreeBS
dc.description.departmentInfectious Diseases
dc.description.majorBiology
dc.description.advisorJulie Moore
dc.description.committeeJulie Moore
dc.description.committeeDavid Peterson


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record