SBIR/STTR Research Award

Covalent Vaccine for HIV

Award identifier bee3dd436c9ceed0afcc2643a7b3fe4fb497e338d739953be46f8591c5604a8fAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$600,000

Program and phase

STTR · Phase I

Award year

2011

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
COVALENT BIOSCIENCE INCORPORATED
Proposal award date
Not reported
Contract end date
Not reported
UEI
XV4BBLLMGSY9
Solicitation number
PA10-124
Topic code
NIAID

Research abstract

DESCRIPTION (provided by applicant): We propose a Phase I STTR study to develop a novel human immunodeficiency virus (HIV) vaccine strategy with the potential of world-wide efficacy. The HIV/AIDS pandemic remains a major global burden. No test vaccine based on traditional scientific principles has induced sufficiently protective immunity to HIV. Induction of neutralizing antibodies (Abs), the cornerstone of vaccination against microbes, has been thwarted by: (a) mutability of the immunodominant viral epitopes, and (b) poor adaptive immunological response to conserved epitopes important in virus-host cell interactions. CD4 binding by the HIV envelope glycoprotein gp120 is an obligatory step in the HIV life cycle. gp120 residues 421-433 constitute the mostly-conserved core of the CD4 binding site (CD4BScore). Except for rare survivors of prolonged HIV infection, the immune system does not support the production of anti-CD4BScore Abs. The proposed Phase I project focuses on electrophilic immunogens (E-immunogens) derived from the novel chemical engineering strategy termed Covalent Vaccination concept. E-immunogens hold the potential of inducing the synthesis of protective Abs that is beyond the scope of the physiological immune response. We will carry out the following developmental studies: (i) Characterize and compare the protective anti-HIV properties of rabbit and mouse antibodies raised by immunization with electrophilic derivatives of purified gp120 and synthetic 416-433 peptide; (ii) Maximize the antibody response to the lead E-immunogen using alternate adjuvants. Proving preclinical proof-of-principle for covalent vaccination as an effective approach in the present project is an important step in translating this approach for HIV vaccination.PUBLIC HEALTH RELEVANCE: This project is directed toward developing a novel vaccine strategy for HIV infection. If the strategy is proven valid, the project holds the potential of contributing a candidate HIV vaccine suitable for advanced preclinical studies and commercial development.

Technology keywords

Not reported

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Agency intelligence

Department of Health and Human Services

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