The overall objective for Project 1 is to enhance the immunogenicity and efficacy ofrAAV/HIV vaccines.We have shown that a single dose of a first generation SIV vaccine based on rAAV serotype 2 (rAAV2) vectors is highly immunogenic in rhesus macaques. These same vaccines significantly reduced viral burden in macaques after challenge with pathogenic SIV. More recently, we have shown that another serotype (rAAV1) is 1 - 2 orders of magnitude better at gene delivery to muscle than rAAV2. These observations suggest that: (i) the current first generation vaccine is probably sub-optimal; (ii) alternate serotype vectors might allow for dramatic increases in transduction (and immunogenicity); and, (iii) alternate serotype vectors offer the possibility of 'prime-boost' regimens where the induction of vector cross-neutralizing antibodies is avoided.
In Specific Aim 1, we will extend these observations by testing prime-boost regimens using alternate serotypes (rAAV1 and rAAV5) that are more efficient than rAAV2 at gene transfer and are genetically distinct in the capsid gene (no cross-reacting antibodies). We will also examine the effects of pre-existing immunity to AAV on the immunogenicity of rAAWSIV (and HIV) vaccines in macaques, in addition to vector enhancements, we have tested 'non-traditional' molecular adjuvants to augment immune responses engendered by rAAV vaccines and have identified promising candidates.
In Specific Aim 2, we will advance these candidates into immunogenicity trials in macaques.Building on the data from this Project, we will design and test a second generation vaccine in immunogenicity and challenge experiments in macaques. A final challenge trial will be combined with a trial proposed in Project 4 wherein the second generation rAAV vaccine will be combined with an rAAV vector that directs the expression of antibody genes that neutralize primary isolates of HIV- 1.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
2P01AI056354-02
Application #
6852995
Study Section
Special Emphasis Panel (ZAI1-CL-A (M4))
Project Start
2004-09-29
Project End
2006-08-31
Budget Start
2004-09-30
Budget End
2005-08-31
Support Year
2
Fiscal Year
2004
Total Cost
$703,121
Indirect Cost
Name
Nationwide Children's Hospital
Department
Type
DUNS #
147212963
City
Columbus
State
OH
Country
United States
Zip Code
43205
Clark, K Reed; Walsh, Scott T R (2009) Crystal structure of a 3B3 variant--a broadly neutralizing HIV-1 scFv antibody. Protein Sci 18:2429-41
Chen, Chun-Liang; Jensen, Ryan L; Schnepp, Bruce C et al. (2005) Molecular characterization of adeno-associated viruses infecting children. J Virol 79:14781-92
Johnson, Philip R; Schnepp, Bruce C; Connell, Mary J et al. (2005) Novel adeno-associated virus vector vaccine restricts replication of simian immunodeficiency virus in macaques. J Virol 79:955-65