Scott W. Wong, Ph.D.
- Professor, VGTI-Vaccine and Gene Therapy Institute
- Molecular Microbiology and Immunology Graduate Program, School of Medicine
- Program in Molecular and Cellular Biosciences, School of Medicine
Biography
Dr. Wong received his Ph.D. from Stanford University School of Medicine in 1987 studying eukaryotic DNA replication. Upon completing his degree he performed post-doctoral research at Stanford University and later at Harvard Medical School, where he focused on human herpesvirus replication and pathogenesis. He came to the Oregon Regional Primate Research Center in 1991 as an Assistant Scientist in the Division of Pathobiology and Immunology, and is now a Senior Scientist and interim Division Chief. Dr. Wong’s primary appointment is in the Vaccine and Gene Therapy Institute, where he is a Senior Scientist and a Professor of Molecular Microbiology and Immunology in the OHSU School of Medicine.
Understanding how viruses cause disease is important to the development of effective antiviral therapies and potential vaccines.
The long-term goal of the Wong laboratory is to understand how viruses cause disease. This is important in developing effective antiviral therapies and potential vaccines. The Wong lab is currently investigating two types of viruses: orthopoxviruses, which induce disease similar to smallpox; and herpesviruses, which can induce severe disease in individuals. Some of these viruses are very specific for their natural hosts, a factor that complicates the ability to study the mechanisms of the human viruses in an animal model. An alternative approach is to utilize animal models that harbor viruses that are closely related to the human virus. One animal model that has proven to be invaluable in understanding the mechanisms of infectious disease and for vaccine development is the nonhuman primate.
By employing molecular, genetic and virological techniques, members of Dr. Wong’s laboratory examine how these nonhuman primate viruses infect and replicate in cell culture and eventually how they cause illnesses in vivo. They have shown that experimental inoculation of normal monkeys with orthopoxviruses causes disease that is virtually identical to smallpox and have identified novel viral proteins utilizing proteomic analysis that may facilitate disease. Additionally, experimental infection of immunocompromised monkeys with simian herpesviruses results in disease manifestations that closely resemble those observed in humans infected with the human immunodeficiency virus (HIV). Utilizing these techniques they are identifying the viral determinants that contribute to disease and are devising novel recombinant molecules to help prevent viral pathogenesis.
Education and training
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Degrees
- Ph.D., 1987, Stanford University School of Medicine
Areas of interest
- HIV pathogenesis and vaccine development
Publications
Selected publications
- Skalsky RL, Barr SA, Jeffery AJ, Blair T, Estep R, Wong SW. Japanese Macaque Rhadinovirus Encodes a Viral MicroRNA Mimic of the miR-17 Family. JVirol. 2016 Sep 29;90(20):9350-63. doi: 10.1128/JVI.01123-16. PMID: 27512057, PMCID: PMC5044857
- Blair TC, Manoharan M, Rawlings-Rhea SD, Tagge I, Kohama SG,Hollister-Smith J, Ferguson B, Woltjer RL, Frederick MC, Pollaro J, Rooney WD,Sherman LS, Bourdette DN, Wong SW. Immunopathology of Japanese macaque encephalomyelitis is similar to multiple sclerosis. J Neuroimmunol. 2016 Feb15;291:1-10. doi: 10.1016/j.jneuroim.2015.11.026. PMID: 26857488, PMCID: PMC4748211
- Morin G, Robinson BA, Rogers KS, Wong SW.;A Rhesus Rhadinovirus Viral Interferon (IFN) Regulatory Factor Is Virion Associated and Inhibits the Early IFN Antiviral Response. J Virol. 2015 Aug;89(15):7707-21.doi: 10.1128/JVI.01175-15. PMID: 25972548, PMCID: PMC4505633
Publications
Generation of chimeric forms of rhesus macaque rhadinovirus expressing KSHV envelope glycoproteins gH and gL for utilization in an NHP model of infection
Journal of virologyKaposi’s sarcoma-associated herpesvirus (KSHV) gB dictates a low-pH endocytotic entry pathway as revealed by a dual-fluorescent virus system and a rhesus monkey rhadinovirus expressing KSHV gB
PLoS pathogensMultivalent MVA-vectored vaccine elicits EBV neutralizing antibodies in rhesus macaques that reduce EBV infection in humanized mice
Frontiers in immunologyRapamycin limits CD4+ T cell proliferation in simian immunodeficiency virus-infected rhesus macaques on antiretroviral therapy
Journal of Clinical InvestigationMembrane-associated and secreted forms of the rhesus macaque rhadinovirus-encoded CD200 homologue and cellular CD200 demonstrate differential effects on rhesus macaque CD200 receptor signaling and regulation of myeloid cell activation
Journal of virologyMRI characteristics of Japanese macaque encephalomyelitis
Journal of NeuroimagingMyelin-specific T cells in animals with Japanese macaque encephalomyelitis
Annals of Clinical and Translational NeurologyMolecular analysis of lymphoid tissue from rhesus macaque rhadinovirus-infected monkeys identifies alterations in host genes associated with oncogenesis
PloS oneRhesus macaque rhadinovirus encodes a viral interferon regulatory factor to disrupt promyelocytic leukemia nuclear bodies and antagonize type I interferon signaling
Journal of virologyRole of IL-15 signaling in the pathogenesis of simian immunodeficiency virus infection in rhesus macaques
Journal of ImmunologyGammaherpesvirus infection and malignant disease in rhesus macaques experimentally infected with SIV or SHIV
PLoS pathogensImmunopathology of Japanese macaque encephalomyelitis is similar to multiple sclerosis
Journal of NeuroimmunologyJapanese macaque rhadinovirus encodes a viral microRNA mimic of the miR-17 family
Journal of virologyA rhesus rhadinovirus viral interferon (IFN) regulatory factor is virion associated and inhibits the early IFN antiviral response
Journal of virologyA simian hemorrhagic fever virus isolate from persistently infected baboons efficiently induces hemorrhagic fever disease in Japanese macaques
VirologyBoHV-4-based vector single heterologous antigen delivery protects STAT1(-/-) mice from monkeypoxvirus lethal challenge
PLoS neglected tropical diseasesT Cell Inactivation by Poxviral B22 Family Proteins Increases Viral Virulence
PLoS pathogensThe rhesus rhadinovirus CD200 homologue affects immune responses and viral loads during in vivo infection
Journal of virologyGenomic characterization of japanese macaque rhadinovirus, a novel herpesvirus isolated from a nonhuman primate with a spontaneous inflammatory demyelinating disease
Journal of virologyNeisseria infection of rhesus macaques as a model to study colonization, transmission, persistence, and horizontal gene transfer
Proceedings of the National Academy of Sciences of the United States of AmericaViral interferon regulatory factors are critical for delay of the host immune response against rhesus macaque rhadinovirus infection
Journal of virologyViral interferon regulatory factors decrease the induction of type I and type II interferon during rhesus macaque rhadinovirus infection
Journal of virology