A novel DC-targeting non-integrating lentivector vaccine for HIV infection

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$600,000.00
Award Year:
2010
Program:
SBIR
Phase:
Phase I
Contract:
1R43AI087444-01
Award Id:
95757
Agency Tracking Number:
AI087444
Solicitation Year:
n/a
Solicitation Topic Code:
NIAID
Solicitation Number:
n/a
Small Business Information
1124 COLUMBIA ST SUITE 719, SEATTLE, WA, -
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
831016907
Principal Investigator:
SCOTT ROBBINS
(206) 453-5252
SROBBINS@TRIABIO.COM
Business Contact:
CHRISTOPHER CLEGG
() -
cclegg@triabio.com
Research Institution:
n/a
Abstract
DESCRIPTION (provided by applicant): Despite two decades of persistent research on prophylactic and therapeutic immunization against HIV, an effective vaccine-based solution to the HIV pandemic has remained elusive. However, the last few years have provide d important insights into the type of immune response that would be required for an effective HIV vaccine. For instance, in studies of natural HIV infection, T cell responses to the Gag protein are associated with lower viral load, and nonhuman primates (N HP) that mount robust Gag-specific T cell responses after immunization are more likely to survive after challenge with SIV. Immune Design Corp (IDC) is developing a vaccine platform around a novel DC-targeting non-integrating lentivector (DC-NILV). Using t his delivery system, one can efficiently express antigens in DCs and elicit unprecedented CD8 T cell immune responses after a single administration. The ultimate goal of this project proposal is to establish a foundation for a DC-NILV-based HIV vaccine by developing and testing a DC-NILV SIV vaccine analogue for use in future NHP-SIV challenge studies. To accomplish this goal, we have chosen SIVMAC251-Gag and -Nef antigens encoded and delivered by our DC-NILV platform as vaccine candidates. To initiate this work, we will first develop a mid-scale DC-NILV production process based on the small-scale process currently in place, while establishing product release assays to assess vector quality and safety. Once these processes are established, we will optimize v accine delivery for maximal immunogenicity in mice using assays that measure CD8 and CD4 T cell responses against SIV-Gag and -Nef. Finally, we will test the immunogenicity of SIV-Gag and -Nef when delivered via our vaccine platform in rhesus monkeys. Duri ng the course of the study, significant emphasis will be placed on the magnitude, breadth, and polyfunctionality of the ensuing immune responses as these characteristics are currently perceived to be the best correlates for long-term protective T cell-medi ated immunity. The overall success of the study will primarily be measured using the following criteria: 1) The delivery of SIV antigens via DC-NILV provides and effective mechanism to generate CD8 T cell responses in NHP; 2) There is value in homologous D C-NILV prime-boost vaccine regimens for the generation of protective T cell-mediated immunity; and 3) The inclusion of multiple antigens within a single DC-NILV is able to expand the diversity of the ensuing immune response without compromising the respons e against individual protein antigens. PUBLIC HEALTH RELEVANCE: There is an unmet medical need for an effective vaccine against HIV as previous attempts have failed, most likely due to their inability to induce protective T cell responses. We are de veloping a novel vaccine vector that leads to robust T cell activation by delivering antigens directly to dendritic cells, the key cell type for initiation of adaptive immunity and memory. This vaccine vector has the potential to have great protective effi cacy against HIV infection in humans.

* information listed above is at the time of submission.

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