EPIDEMIOLOGY OF HPV-RELATED SCSC IN TRANSPLANT PATIENTS
EPIDEMIOLOGY OF HPV-RELATED SCSC IN TRANSPLANT PATIENTS
批准号:
8307527
负责人:
MARGARET M MADELEINE
金额:
$43.17万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-07-01 至 2013-06-30
关键词:
AddressAffectAgingAnogenital cancerAntibodiesAntibody FormationAreaBiological AssayBiologyBloodCardiacCellular ImmunityCervicalClinical TrialsCollaborationsDNA FingerprintingDataDatabasesDoctor of PhilosophyDoseEpidemiologyEtiologyEye ColorEyebrow structureFutureGenital systemHairHuman Papilloma Virus VaccineHuman PapillomavirusHuman papilloma virus infectionImmunocompetentImmunosuppressionImmunosuppressive AgentsIncidenceInterviewKidneyKineticsLaboratoriesLifeLinkLongitudinal StudiesMalignant NeoplasmsMalignant Squamous Cell NeoplasmMalignant neoplasm of cervix uteriMeasuresModelingMolecular BiologyMolecular EpidemiologyMorbidity - disease rateNeoplasmsNested Case-Control StudyOrgan TransplantationPathway interactionsPatientsPersonsPharmaceutical PreparationsPlayPopulationPrevalencePreventionPrincipal InvestigatorPublicationsQuality of lifeRecording of previous eventsResearch DesignResourcesRiskRisk FactorsRoleSamplingSerologic testsSerumSignal TransductionSkinSkin CancerSquamous CellSquamous Cell NeoplasmsSteroidsSun ExposureTechniquesTestingTherapeutic immunosuppressionTimeTransplant RecipientsTransplantationVaccinesViralVisitWorkage groupclinical epidemiologyclinically significantcohorteconomic costexperiencehigh riskinsightinterdisciplinary collaborationmembermortalitypopulation basedpreventprogramsprophylacticprospectivesample collectionsound
中文摘要
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英文摘要
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The observation that HPV-related cancers may be linked to immunosuppression has led us to focus this
competitive renewal on a population that is receiving strong immunosuppressive drugs for extended periods
of time, i.e., renal and cardiac organ transplant patients (OTR). These patients experience a high incidence
of what may be an HPV-associated cancer, squamous cell skin cancer (SCSC). We posit that transplant
populations are the best model to study the effect of immunosuppression on HPV infection and the
association between HPV and SCSC because transplant patients are now living longer with theirtransplants,
the prevalence of SCSC sharply increases with time since transplant, these patients often have multiple and
aggressive SCSC tumors, and SCSC will ultimately affect the majority of transplant patients. In this project
we propose two complementary but separate population-based studies to investigate the role of HPV in renal
and cardiac OTR. The first study we propose is a nested case-control study that will be able to assess 1) if
there are high-risk genus beta HPV types that are associated with an increased risk of SCSC; 2) whether
pre-transplant HPV antibodies predict SCSC; and 3) if patient risk factor data (including history of sun
exposure, skin type, eye color, medication use, and other exposures) gathered in an in-person interview and
integrated with measures of genus beta HPV types together predict which patients are at increased risk of
SCSC. The second study is a longitudinal study designed to explore the kinetics of HPV infection with
repeated sample collection over a 2-year period, starting with a pre-transplant sample. All patients
transplanted in 2008 and 2009 who are residents of the local area will be invited to participate. In this
longitudinal study we will assess 1) whether the number of HPV DNA types, antibody response, or viral
persistence increases with time since transplant and 2) the effect of changes in levels of cell-mediated
immunity on HPV infection status (as measured by various markers of HPV) over time. Our HPV Program
Project group has a long track record of interdisciplinary collaboration, and we plan to develop a new
direction for our work that employs recently developed laboratory techniques that are specific to studying
genus beta HPV types.. Our studies may contribute to a more complete understanding of the role of genus
beta HPV types in SCSC and the role immunosuppression plays in HPV activation. If a strong link between
specific HPV types and SCSC can be verified, there may be evidence to suggest clinical trials of HPV
vaccines to modify the risk of SCSC in OTR.
Lay Summary: This study will examine the risk of squamous cell skin cancer and its relationship to human
papillomavirus in a high-risk group. If a clear association can be shown in this study and others like it, future
work could explore prevention and treatment of this type of skin cancer in different populations.
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Clinical Trials Program
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批准号:10020373
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项目类别:
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资助金额:$53.27万
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财政年份:2019
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负责人:MARGARET M MADELEINE
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依托单位:
Clinical Trials Program
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批准号:10224783
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项目类别:
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资助金额:$19.96万
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财政年份:2019
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依托单位:
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项目类别:
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财政年份:2019
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依托单位:
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批准号:10470116
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项目类别:
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资助金额:$5.64万
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依托单位:
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批准号:10689735
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负责人:MARGARET M MADELEINE
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依托单位:
Clinical Trials Program
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批准号:10601389
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项目类别:
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资助金额:$25.72万
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财政年份:2019
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依托单位:
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批准号:10470114
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项目类别:
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资助金额:$5.04万
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财政年份:2019
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负责人:MARGARET M MADELEINE
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依托单位:
Clinical Trials Program
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批准号:10689736
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项目类别:
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资助金额:$40.16万
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财政年份:2019
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负责人:MARGARET M MADELEINE
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依托单位:
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批准号:10601388
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项目类别:
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资助金额:$20.96万
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财政年份:2019
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负责人:MARGARET M MADELEINE
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依托单位:
Therapeutic use of HPV L1 Vaccine in Anogenital Neoplasia: VIVA Trial
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批准号:9220396
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项目类别:
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资助金额:$76.78万
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财政年份:2017
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负责人:MARGARET M MADELEINE
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依托单位:
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项目类别:
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财政年份:2017
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负责人:MARGARET M MADELEINE
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依托单位:
Therapeutic use of HPV L1 Vaccine in Anogenital Neoplasia: VIVA Trial
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批准号:10230257
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项目类别:
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资助金额:$25.14万
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财政年份:2017
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负责人:MARGARET M MADELEINE
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依托单位:
Therapeutic use of HPV L1 Vaccine in Anogenital Neoplasia: VIVA Trial
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批准号:10113554
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项目类别:
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资助金额:$22.72万
-
财政年份:2017
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负责人:MARGARET M MADELEINE
-
依托单位:
Therapeutic use of HPV L1 Vaccine in Anogenital Neoplasia: VIVA Trial
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批准号:10359814
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项目类别:
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财政年份:2017
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依托单位:
Post GWA Analysis of Inflammation Pathways in Barrett's and Esophageal Cancer
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项目类别:
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财政年份:2014
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负责人:MARGARET M MADELEINE
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依托单位:
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财政年份:2011
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负责人:MARGARET M MADELEINE
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财政年份:2007
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Inflammation Pathways in Breast Cancer
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财政年份:2007
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依托单位:
海外基金