Cocaine abuse continues to be a pressing health and sociological problem confronting many developed nations. In America, thousands of new users are added each day and each year a large proportion die from overdose or other toxic influences. The effects on the unborn can be especially tragic. Significantly, abuse is detrimental not only to the well-being of the individual, but also effects others and degrades the infrastructure of society. The biochemistry of the action of cocaine is complex having perhaps the most unique and powerful reinforcing properties of any drug. While a number of pharmaceuticals have been evaluated, none have proven to be adequate. Hence, there remains no concrete medical solution to the cocaine problem and it has become obvious that alternative avenues must be explored. One such approach invokes immunological strategies for the direct treatment of cocaine abuse and addiction in preventative or rehabilitative contexts. In this way, social programs would be bolstered by an objective scientific foundation. We recently demonstrated the efficacy of an immunological strategy in rat behavioral paradigms using an anticocaine vaccine and a cocaine-binding monoclonal antibody (mAb). This proposal delineates the methodology necessary to 1) complete the current passive immunization aspect of our program by obtaining human and/or humanized anticocaine mAbs for eventual clinical application, and 2) implement catalytic anticocaine mAbs as an additional potent passive immunization protocol. With regard to the latter, we have preliminary data on catalytic mAbs that degrade cocaine and have new hapten designs and strategies for acquiring catalysts with the activity necessary to address cocaine addiction. Significantly, antibodies will be available from murine immunization and from combinatorial antibody libraries that would directly provide human mAbs. All mAbs would enter into our well-established rat models for the human condition. The work described herein provides the culmination in what will be a complete program for the immunopharmacotherapy of cocaine abuse.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA008590-10
Application #
6637117
Study Section
Human Development Research Subcommittee (NIDA)
Program Officer
Shih, Ming L
Project Start
1994-01-01
Project End
2005-07-31
Budget Start
2003-08-01
Budget End
2005-07-31
Support Year
10
Fiscal Year
2003
Total Cost
$370,400
Indirect Cost
Name
Scripps Research Institute
Department
Type
DUNS #
781613492
City
La Jolla
State
CA
Country
United States
Zip Code
92037
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Bremer, Paul T; Janda, Kim D (2017) Conjugate Vaccine Immunotherapy for Substance Use Disorder. Pharmacol Rev 69:298-315
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Wenthur, Cody J; Cai, Xiaoqing; Ellis, Beverly A et al. (2017) Augmenting the efficacy of anti-cocaine catalytic antibodies through chimeric hapten design and combinatorial vaccination. Bioorg Med Chem Lett 27:3666-3668
Kimishima, Atsushi; Wenthur, Cody J; Eubanks, Lisa M et al. (2016) Cocaine Vaccine Development: Evaluation of Carrier and Adjuvant Combinations That Activate Multiple Toll-Like Receptors. Mol Pharm 13:3884-3890
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Lockner, Jonathan W; Eubanks, Lisa M; Choi, Jennifer L et al. (2015) Flagellin as carrier and adjuvant in cocaine vaccine development. Mol Pharm 12:653-62
Collins, K C; Schlosburg, J E; Lockner, J W et al. (2014) Lipid tucaresol as an adjuvant for methamphetamine vaccine development. Chem Commun (Camb) 50:4079-81
Collins, Karen C; Janda, Kim D (2014) Investigating hapten clustering as a strategy to enhance vaccines against drugs of abuse. Bioconjug Chem 25:593-600

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