The long-term objective of this project is to develop antibody-based medications for the treatment of medical problems caused by abuse of methamphetamine ((+)METH)), amphetamine and ecstasy. Abuse of these chemicals can lead to disruption of families, psychosis, cardiovascular problems, and death. It is envisioned that these new medications could be used for treating a range of medical problems associated with synthetic stimulant abuse (e.g., drug overdose, addiction). Although medicines are sorely needed, these drugs and their active metabolites present a challenging problem for the development of effective medications. The experiments in this proposal are designed to address these problems by discovering anti-drug monoclonal antibodies (mAb, both mouse and human) that recognize and neutralize the in vivo effects of these dangerous chemicals. The selection criteria for the mAb medications will include high affinity drug binding, refined specificity for METH-like drugs and metabolites, and in vivo testing for their ability to prevent brain penetration of these chemicals. In complementary studies, the best mAb prototypes will be used to generate single chain antibodies (scFv) by linking the heavy and light chain variable region sequences through a spacer group. Research with these smaller binding proteins will include two separate areas. First, in vitro protein translation techniques will be used to screen for scFv with improved affinity and specificity. Second, the scFv will be chemically modified with poly(ethylene glycol) to allow control of the pharmacokinetic properties. Since scFv are much smaller than intact mAb and are engineered as a single gene product, they could eventually lead to less expensive medications. Through careful design of METH-like haptens, generation of mouse and human mAb, and advanced molecular engineering technology, this research program will produce novel protein-based medications with optimal immunological and pharmacological properties. Because all of these medications can neutralize drug effects without entering the brain, they offer an innovative and unique approach to treating medical problems resulting from stimulant abuse.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA011560-07
Application #
6895100
Study Section
Special Emphasis Panel (ZDA1-RXL-E (10))
Program Officer
Chiang, Nora
Project Start
1998-01-05
Project End
2009-03-31
Budget Start
2005-04-01
Budget End
2006-03-31
Support Year
7
Fiscal Year
2005
Total Cost
$518,803
Indirect Cost
Name
University of Arkansas for Medical Sciences
Department
Pharmacology
Type
Schools of Medicine
DUNS #
122452563
City
Little Rock
State
AR
Country
United States
Zip Code
72205
Hambuchen, Michael D; Rüedi-Bettschen, Daniela; Gunnell, Melinda G et al. (2016) Chronic treatment of (+)-methamphetamine-induced locomotor effects in rats using one or a combination of two high affinity anti-methamphetamine monoclonal antibodies. Hum Vaccin Immunother 12:2240-8
Hambuchen, Michael D; Carroll, F Ivy; Rüedi-Bettschen, Daniela et al. (2015) Combining Active Immunization with Monoclonal Antibody Therapy To Facilitate Early Initiation of a Long-Acting Anti-Methamphetamine Antibody Response. J Med Chem 58:4665-77
Milesi-Hallé, Alessandra; Hambuchen, Michael D; McMillan, Donald E et al. (2015) The pharmacokinetics of methamphetamine self-administration in male and female rats. Drug Alcohol Depend 150:164-9
Peterson, Eric C; Gentry, W Brooks; Owens, S Michael (2014) Customizing monoclonal antibodies for the treatment of methamphetamine abuse: current and future applications. Adv Pharmacol 69:107-27
White, Sarah J; Hendrickson, Howard P; Atchley, William T et al. (2014) Treatment with a monoclonal antibody against methamphetamine and amphetamine reduces maternal and fetal rat brain concentrations in late pregnancy. Drug Metab Dispos 42:1285-91
Laurenzana, Elizabeth M; Stevens, Misty W; Frank, John C et al. (2014) Pharmacological effects of two anti-methamphetamine monoclonal antibodies. Supporting data for lead candidate selection for clinical development. Hum Vaccin Immunother 10:2638-47
Hambuchen, Michael D; Rüedi-Bettschen, Daniela; Williams, D Keith et al. (2014) Treatment of rats with an anti-(+)-methamphetamine monoclonal antibody shortens the duration of action of repeated (+)-methamphetamine challenges over a one month period. Vaccine 32:6213-9
Owens, S Michael; Atchley, William T; Hambuchen, Michael D et al. (2011) Monoclonal antibodies as pharmacokinetic antagonists for the treatment of (+)-methamphetamine addiction. CNS Neurol Disord Drug Targets 10:892-8
Hubbard, Jonathan J; Laurenzana, Elizabeth M; Williams, D Keith et al. (2011) The fate and function of therapeutic antiaddiction monoclonal antibodies across the reproductive cycle of rats. J Pharmacol Exp Ther 336:414-22
Carroll, F Ivy; Blough, Bruce E; Pidaparthi, Ramakrishna R et al. (2011) Synthesis of mercapto-(+)-methamphetamine haptens and their use for obtaining improved epitope density on (+)-methamphetamine conjugate vaccines. J Med Chem 54:5221-8

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