The studies done in this Project will carefully interdigitate the findings of Projects 1 and 2 into appropriate animal model systems to test candidate vaccine strains. The objectives are as follows: First, genetically engineered mutants from Project 1 will be tested initially in mice and subsequently in guinea pigs to determine their capacity to replicate in the CNS, peripheral tissue, to establish latency, to cause recurrent lesions in guinea pigs, to reactivate upon explantation from ganglia, and to protect these animal species from challenge with virulent viruses. These studies will aid in the design of prototype vaccines strains based on the results of studies in Projects 1 and 3. Second, once candidate vaccine strains become identified, extensive challenge studies in mice and guinea pigs will be done utilizing different routes of immunization and challenge. Successful challenge will be further correlated with systemic and mucosal immune responses. Third, attempts to enhance systemic and mucosal immunity by novel and careful employment of interleukins in feasibility experiments will be initiated. These experiments will utilize IL-4, IL-5, and/or IL-6 before immunization to determine its effects on immune response. If immunity can be enhanced without evidence of adverse effects, an attempt will be made to evaluate recombinant viruses carrying IL genes under various promoters. The knowledge gained from these studies will provide a basis for more detailed animal safety and immunogenicity studies in anticipation of human trials.

Project Start
Project End
Budget Start
Budget End
Support Year
9
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Chicago
Department
Type
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
Hellums, Elizabeth K; Markert, James M; Parker, Jacqueline N et al. (2005) Increased efficacy of an interleukin-12-secreting herpes simplex virus in a syngeneic intracranial murine glioma model. Neuro Oncol 7:213-24
Whitley, Richard J (2003) Smallpox: a potential agent of bioterrorism. Antiviral Res 57:7-12
Whitley, Richard J; Roizman, Bernard (2002) Herpes simplex viruses: is a vaccine tenable? J Clin Invest 110:145-51
Whitley, Richard J; Gnann, John W (2002) Viral encephalitis: familiar infections and emerging pathogens. Lancet 359:507-13
Markert, J M; Parker, J N; Gillespie, G Y et al. (2001) Genetically engineered human herpes simplex virus in the treatment of brain tumours. Herpes 8:17-22
Parker, J N; Gillespie, G Y; Love, C E et al. (2000) Engineered herpes simplex virus expressing IL-12 in the treatment of experimental murine brain tumors. Proc Natl Acad Sci U S A 97:2208-13
Markert, J M; Gillespie, G Y; Weichselbaum, R R et al. (2000) Genetically engineered HSV in the treatment of glioma: a review. Rev Med Virol 10:17-30
Tran, L C; Kissner, J M; Westerman, L E et al. (2000) A herpes simplex virus 1 recombinant lacking the glycoprotein G coding sequences is defective in entry through apical surfaces of polarized epithelial cells in culture and in vivo. Proc Natl Acad Sci U S A 97:1818-22
Whitley, R J; Kimberlin, D W; Roizman, B (1998) Herpes simplex viruses. Clin Infect Dis 26:541-53;quiz 554-5
Kimberlin, D W; Whitley, R J (1998) Human herpesvirus-6: neurologic implications of a newly-described viral pathogen. J Neurovirol 4:474-85

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