This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Since the life span of the world population is increasing, health complications as a result of immune senescence will undoubtedly increase as well. Amongst these complications is herpes zoster (shingles) caused by the reactivation of Varicella Zoster Virus. The currently approved zoster vaccine (ZosterVax from Merck) reduces the incidence of herpes zoster by 50%. Therefore, 50% of this population remains susceptible to zoster and its ensuing neurological complications. Studies to improve the efficacy and safety of this vaccine require an improved understanding of the immune response to VZV during different stages of the disease. However, these studies are complicated since an experimental animal model that can recapitulate both the acute (varicella, chickenpox) and reactivation (zoster) forms of the disease is currently not available. An alternative is to utilize a nonhuman primate (NHP) model that is susceptible to infection by the closely related virus Simian varicella virus (SVV). Indeed, considerable clinical and molecular similarities between SVV and VZV indicate that SVV infection of NHP has considerable potential as an animal model. We have recently shown that infection of rhesus macaques with SVV recapitulates the hallmarks of VZV infection in humans including: the development of varicella rash, humoral and cellular immunity, resolution of acute viremia and the establishment of latency in sensory ganglia. This novel model will allow a deeper understanding of the immune deficiencies that underlie VZV reactivation in elderly subjects, which in turn will facilitate the design of efficacious vaccines to boost specific aspects of VZV immune surveillance.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
5P51RR000163-51
Application #
8173218
Study Section
Special Emphasis Panel (ZRR1-CM-8 (01))
Project Start
2010-05-01
Project End
2011-04-30
Budget Start
2010-05-01
Budget End
2011-04-30
Support Year
51
Fiscal Year
2010
Total Cost
$47,603
Indirect Cost
Name
Oregon Health and Science University
Department
Type
Schools of Medicine
DUNS #
096997515
City
Portland
State
OR
Country
United States
Zip Code
97239
Okoye, Afam A; Hansen, Scott G; Vaidya, Mukta et al. (2018) Early antiretroviral therapy limits SIV reservoir establishment to delay or prevent post-treatment viral rebound. Nat Med 24:1430-1440
Jensen, Jeffrey T; Hanna, Carol; Mishler, Emily et al. (2018) Effect of menstrual cycle phase and hormonal treatments on evaluation of tubal patency in baboons. J Med Primatol 47:40-45
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Moccetti, Federico; Brown, Eran; Xie, Aris et al. (2018) Myocardial Infarction Produces Sustained Proinflammatory Endothelial Activation in Remote Arteries. J Am Coll Cardiol 72:1015-1026
Blue, Steven W; Winchell, Andrea J; Kaucher, Amy V et al. (2018) Simultaneous quantitation of multiple contraceptive hormones in human serum by LC-MS/MS. Contraception 97:363-369
Jeon, Sookyoung; Li, Qiyao; Rubakhin, Stanislav S et al. (2018) 13C-lutein is differentially distributed in tissues of an adult female rhesus macaque following a single oral administration: a pilot study. Nutr Res :
Slayden, Ov Daniel; Friason, Francis Kathryn E; Bond, Kise Rosen et al. (2018) Hormonal regulation of oviductal glycoprotein 1 (OVGP1; MUC9) in the rhesus macaque cervix. J Med Primatol 47:362-370
Dissen, G A; Adachi, K; Lomniczi, A et al. (2017) Engineering a gene silencing viral construct that targets the cat hypothalamus to induce permanent sterility: An update. Reprod Domest Anim 52 Suppl 2:354-358

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