The general goal of this program is to use herpesvirus recombinants as vectors for the expression of SIV proteins to provide safe, effective vaccines against AIDS viruses. Our hypothesis is that herpesviruses can be genetically modified to provide safe viral vectors for AIDS vaccines that possess some of the some biological properties as AIDS viruses First, herpes viruses can persist in the host and periodically reactive, providing periodic responses in mouse model systems. Even replication-defective herpes strains seem to induce durable immune responses in mouse model systems. Second, herpes viruses activate a strong cellular immune response without the risk of killing T cells. Thus, our hope is that the herpesvirus recombinant vectors can induce a robust cellular response against AIDS virus antigens that is continually activated and eliminate any HIV or SIV infected cell soon after infection. The goal of the first project, entitled """"""""Herpes Simplex Virus as an AIDS Vaccine Vector,"""""""" is to use herpes simplex virus type 2 as a vaccine vector to express SIV env and gag proteins using replication-defective and replication competent strains of HSV-2 and rev-independent SIV gag and env genes. The goal of the second project, entitled """"""""Construction of Rhesus Rhadinovirus Vaccine Vectors,"""""""" is to construct and analyze replication-competent strains of rhesus monkey rhadinovirus (RRV) that express SIV antigens at high levels. The goal of the third project, entitled """"""""Herpesvirus Vectors as Vaccines in Rhesus Monkeys,"""""""" is to utilize the recombinants constructed in Projects 1 and 2 for vaccine/challenge experiments in rhesus monkeys. Humoral and cellular immune response against SIV and herpesviral antigens will be measured. projection against various forms of SIV challenge will be measured. Through these studies we hope to construct prototype vaccines against SIV which can be translated into vaccines against HIV. The common approaches for construction of recombinant vectors in herpesviruses and the ability to compare recombinants in a common rhesus monkey model provide unifying themes for this program.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
5P01AI046006-03
Application #
6374264
Study Section
Special Emphasis Panel (ZAI1-KWR-A (M1))
Program Officer
Pensiero, Michael N
Project Start
1999-09-15
Project End
2004-08-31
Budget Start
2001-09-01
Budget End
2002-08-31
Support Year
3
Fiscal Year
2001
Total Cost
$1,057,488
Indirect Cost
Name
Harvard University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
082359691
City
Boston
State
MA
Country
United States
Zip Code
02115
Meythaler, Mareike; Wang, Zichun; Martinot, Amanda et al. (2011) Early induction of polyfunctional simian immunodeficiency virus (SIV)-specific T lymphocytes and rapid disappearance of SIV from lymph nodes of sooty mangabeys during primary infection. J Immunol 186:5151-61
Reszka, Natalia; Zhou, Changhong; Song, Byeongwoon et al. (2010) Simian TRIM5alpha proteins reduce replication of herpes simplex virus. Virology 398:243-50
Meythaler, Mareike; Martinot, Amanda; Wang, Zichun et al. (2009) Differential CD4+ T-lymphocyte apoptosis and bystander T-cell activation in rhesus macaques and sooty mangabeys during acute simian immunodeficiency virus infection. J Virol 83:572-83
Liu, Xueqiao; Broberg, Eeva; Watanabe, Daisuke et al. (2009) Genetic engineering of a modified herpes simplex virus 1 vaccine vector. Vaccine 27:2760-7
Cliffe, Anna R; Garber, David A; Knipe, David M (2009) Transcription of the herpes simplex virus latency-associated transcript promotes the formation of facultative heterochromatin on lytic promoters. J Virol 83:8182-90
Brockman, Mark A; Knipe, David M (2008) Herpes simplex virus as a tool to define the role of complement in the immune response to peripheral infection. Vaccine 26 Suppl 8:I94-9
Cliffe, Anna R; Knipe, David M (2008) Herpes simplex virus ICP0 promotes both histone removal and acetylation on viral DNA during lytic infection. J Virol 82:12030-8
Meythaler, Mareike; Pryputniewicz, Sarah; Kaur, Amitinder (2008) Kinetics of T lymphocyte apoptosis and the cellular immune response in SIVmac239-infected rhesus macaques. J Med Primatol 37 Suppl 2:33-45
Watanabe, Daisuke; Brockman, Mark A; Ndung'u, Thumbi et al. (2007) Properties of a herpes simplex virus multiple immediate-early gene-deleted recombinant as a vaccine vector. Virology 357:186-98
Kaur, Amitinder; Sanford, Hannah B; Garry, Deirdre et al. (2007) Ability of herpes simplex virus vectors to boost immune responses to DNA vectors and to protect against challenge by simian immunodeficiency virus. Virology 357:199-214

Showing the most recent 10 out of 13 publications