SBIR/STTR Research Award

Therapeutic Antibodies for Rabies

Award identifier 4458723e6ee31a64534353484f00ebb6fb74d37f88b9f2999758e9b9d005587eAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$599,752

Program and phase

SBIR · 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
TRELLIS BIOSCIENCE, INC.
Proposal award date
Not reported
Contract end date
Not reported
UEI
LFEJER34NQU6
Solicitation number
PA10-123
Topic code
NIAID

Research abstract

DESCRIPTION (provided by applicant): Trellis Bioscience has developed its patented CellSpot technology into a robust platform for characterizing the secreted antibody from single human lymphocytes with regard to specificity and affinity against multiple antigens. For example, the platform was used to isolate a rare, high quality human antibody to Respiratory Syncytial Virus (RSV) that is now being prepared for human clinical testing by Trellis' licensee, MedImmune. In this project, we propose to use CellSpot to isolate therapeutic antibodies to combat rabies virus (RV) infections. Blood lymphocytes from adults who have been vaccinated against RV will be layered onto an antibody capture surface. After 5 hours of incubation, each cell's secreted antibody forms a footprint in the vicinity of the cell (~150 lt m diameter). These footprints will then be incubated with fluorescent beads conjugated to the antigen target, which in this project will be the G protein of RV. The G protein is the same antigen used inrabies vaccines and has been shown to elicit protective antibodies. There are differences between G proteins of different strains, and there are both homologous, conserved regions and heterologous, variable regions on the G proteins of different RV strains. The most useful monoclonal antibodies are those which react against the broadest set of variant G proteins. Therefore, the antibody footprints will be screened with a panel of distinguishable fluorescent beads conjugated to the G-antigens from differentstrains. Spots that contain antibody to multiple G proteins will be detected under automated microscopic examination and the responsible cells will be isolated, followed by cDNA cloning of the antibody for further characterization following transfection into an expression system. These antibodies will be screened for physiological activity both by an in vitro neutralization assay and by an in vivo animal infection model to measure direct protection from infection. In Phase I of this project, we anticipate isolating ~15 human antibodies to the G protein, of which at least one will be shown to be protective in the animal model, confirming utility by a monoclonal comparable to that provided by immune gamma globulin, the current standard of care. Based on success in this Phase I objective, we will submit a Phase II application to advance the development of this antibody to clinical trial with a particular focus on reducing the cost of manufacturing to be competitive with immune gamma globulin. The overall objective of this project is a therapeutic antibody to RV which is well tolerated and highly effective in protecting against a broad range of RV strains. PUBLIC HEALTH RELEVANCE: This project will use an innovative microscopic cell analysis technology to screen human lymphocytes for cells producing antibodies to the rabies virus G protein. The antibodies selected will have the ability to protect animals and, ultimately humans, during rabies infection and will be developed as new therapeutic agents for thisdisease.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

17 SBIR/STTR records share this UEI (2011–2024). Reported award amounts total $29,248,021. Reported amounts are not federal obligations.

Phases: Phase II, Phase I, Phase II – Direct to Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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