SBIR/STTR Research Award

Human gene knock-in mice and anti-cancer antibodies

Award identifier 93d6b336389b844680edf71d8d41681044521fb6f9c2bdc37c095953c5f49445Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$164,643

Program and phase

STTR · Phase I

Award year

2001

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
ONCOIMMUNE, LTD
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
Not reported
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): Pre-clinical studies in experimental animals have yielded a large array of antibodies capable of inducing anti-tumor immunity in animal models. However, in most cases, progress has been slow in translating the principles learned in animal models into therapy of human cancer. A common obstacle to successful clinical translation is that biological properties of the antibodies specific for given human target molecules cannot be pre-screened in vivo prior to clinical trials. Here we propose to use costimulatory molecule CTLA-4 as a model target to develop a paradigm for screening anti-cancer antibodies for clinical trials. Recent studies have demonstrated that anti-CTLA4 mAbs induce T cell immunity against a variety of cancers in experimental animals. We will use mice with a knock-in ofhuman (hu) CTLA4 gene about to screen for anti-huCTLA4 antibodies that can induce anti-tumor immunity in mice. Those anti-CTLA4 mAbs that induce cancer rejection will be modified for clinical trials in the phase II application. Moreover, our proposed studies may provide a paradigm for the development of antibodies specific for human target molecules with a potential for clinical application. PROPOSED COMMERCIAL APPLICATION: The antibodies screened in the CTLA4 knock-in mice will be capable of inducing immunity by engaging human CTLA4 molecules. Given the success that several laboratories have had in the mouse, it is likely that anti-human CTLA4 mAb may induce immunity to multiple lineages of cancer. Moreover, the CTLA4 knock-mice will provide a valuable tool for the production of therapeutic anti-human CTLA4 monoclonal antibodies.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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