KS is a vascular tumor caused by infection with KSHV. The oropharynx plays a central role in KSHV infection. KSHV transmission occurs through saliva which, in sub-Saharan Africa, occurs at high rates beginning in eariy childhood. KSHV replication Is detected most frequently in the oral cavity, and oral viral replication is strongly associated with viremia. Therefore, understanding the biology and pathogenesis of oral KSHV infection appears critical to devising strategies to interrupt transmission and prevent spread throughout the host. This Clinical Core will enroll cohorts and collect biological specimens to support the Program Project, """"""""Oral pathogenesis and host interactions of Kaposi sarcoma-associated herpesvirus (KSHV) infection"""""""" (PI Dr. Timothy Rose). The goal of the Clinical Core is to foster innovative translational research on KSHV infection, replication, pathogenesis and immunity through the collection of uniquely valuable biological specimens from KSHV-infected people in an area hyperendemic for KS. Cohorts will be enrolled at the Uganda Cancer Institute (UCI) in Kampala, Uganda through our outstanding collaborative research group, the Uganda Program on Cancer and Infectious Disease (UPCID). The Clinical Core will be responsible for the enrollment, evaluation, and follow-up of clinical cohorts at the UCI, and for obtaining and managing laboratory specimens for all four projects of this RFA.
Aim 1 of the Clinical Core is to recruit, screen, and enroll KSHV-infected children and adults into research protocols in Kampala, Uganda. Study participants will be enrolled into studies by experienced UPCID research staff. Follow-up of participants will be performed in accordance with the ethical conduct of human subjects research, using proven methods to maximize adherence to study procedures.
Aim 2 is to collect, process, and ship clinical specimens suitable for the study of;(1) KSHV infection of oral epithelial and lymphoid cells using oral tissue collected from routine tonsillectomies;(2) expression of phenotypic markers of angiogenesis and lymphatic differentiation in oral and cutaneous KS tumor biopsies;and (3) immune correlates of the control of KSHV infection using saliva and blood specimens collected from HIV-infected and uninfected subiects followed at the UCI.

Public Health Relevance

KS is the most common malignancy among HIV-infected people worldwide. Most of the population in Uganda and other areas of sub-Saharan Africa are infected with KSHV. In these regions, where HIV infection is also highly prevalent, KS ranks among the most common cancers of adults and children in the general population.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Program Projects (P01)
Project #
1P01DE021954-01
Application #
8142472
Study Section
Special Emphasis Panel (ZDE1-MH (03))
Project Start
Project End
Budget Start
2011-06-07
Budget End
2012-04-30
Support Year
1
Fiscal Year
2011
Total Cost
$176,932
Indirect Cost
Name
Seattle Children's Hospital
Department
Type
DUNS #
048682157
City
Seattle
State
WA
Country
United States
Zip Code
98105
Ikoma, Minako; Gantt, Soren; Casper, Corey et al. (2018) KSHV oral shedding and plasma viremia result in significant changes in the extracellular tumorigenic miRNA expression profile in individuals infected with the malaria parasite. PLoS One 13:e0192659
Garrigues, H Jacques; Howard, Kellie; Barcy, Serge et al. (2017) Full-Length Isoforms of Kaposi's Sarcoma-Associated Herpesvirus Latency-Associated Nuclear Antigen Accumulate in the Cytoplasm of Cells Undergoing the Lytic Cycle of Replication. J Virol 91:
Bruce, A Gregory; Barcy, Serge; DiMaio, Terri et al. (2017) Quantitative Analysis of the KSHV Transcriptome Following Primary Infection of Blood and Lymphatic Endothelial Cells. Pathogens 6:
Sychev, Zoi E; Hu, Alex; DiMaio, Terri A et al. (2017) Integrated systems biology analysis of KSHV latent infection reveals viral induction and reliance on peroxisome mediated lipid metabolism. PLoS Pathog 13:e1006256
Sanchez, Erica L; Pulliam, Thomas H; Dimaio, Terri A et al. (2017) Glycolysis, Glutaminolysis, and Fatty Acid Synthesis Are Required for Distinct Stages of Kaposi's Sarcoma-Associated Herpesvirus Lytic Replication. J Virol 91:
DiMaio, Terri A; Wentz, Breanna L; Lagunoff, Michael (2016) Isolation and characterization of circulating lymphatic endothelial colony forming cells. Exp Cell Res 340:159-69
Bruce, A Gregory; Horst, Jeremy A; Rose, Timothy M (2016) Conservation of the glycoprotein B homologs of the Kaposi?s sarcoma-associated herpesvirus (KSHV/HHV8) and old world primate rhadinoviruses of chimpanzees and macaques. Virology 494:29-46
Lagunoff, Michael (2016) Activation of cellular metabolism during latent Kaposi's Sarcoma herpesvirus infection. Curr Opin Virol 19:45-9
Sanchez, Erica L; Carroll, Patrick A; Thalhofer, Angel B et al. (2015) Latent KSHV Infected Endothelial Cells Are Glutamine Addicted and Require Glutaminolysis for Survival. PLoS Pathog 11:e1005052
Sanchez, Erica L; Lagunoff, Michael (2015) Viral activation of cellular metabolism. Virology 479-480:609-18

Showing the most recent 10 out of 29 publications