Biologics to treat substance use disorders: Current status and new directions

被引:38
|
作者
Pravetoni, Marco [1 ,2 ,3 ]
机构
[1] Minneapolis Med Res Fdn Inc, 701 Pk Ave,S9-920, Minneapolis, MN 55415 USA
[2] Univ Minnesota, Sch Med, Dept Med, Ctr Immunol, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Sch Med, Dept Pharmacol, Ctr Immunol, Minneapolis, MN 55455 USA
关键词
antibodies; adjuvants; biologics; B cell; drug addiction; drug development; delivery; materials; nanoparticles; screening; T cell; vaccines; NICOTINE-SPECIFIC ANTIBODIES; COCAINE MONOCLONAL-ANTIBODY; MORPHINE CONJUGATE VACCINE; INDUCED LOCOMOTOR-ACTIVITY; CD4(+) T-CELLS; MEMORY B-CELLS; SMOKING-CESSATION; MUTATED BUTYRYLCHOLINESTERASE; ADMINISTERED COCAINE; PASSIVE-IMMUNIZATION;
D O I
10.1080/21645515.2016.1212785
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Biologics (vaccines, monoclonal antibodies (mAb), and genetically modified enzymes) offer a promising class of therapeutics to treat substance use disorders (SUD) involving abuse of opioids and stimulants such as nicotine, cocaine, and methamphetamine. In contrast to small molecule medications targeting brain receptors, biologics for SUD are larger molecules that do not cross the blood-brain barrier (BBB), but target its central nervous the drug itself, preventing its distribution to the brain and blunting effects on the system (CNS). Active and passive immunization approaches rely on antibodies (Ab) that bind drugs of abuse in serum and block their distribution to the brain, preventing the rewarding effects of drugs and addiction-related behaviors. Alternatives to vaccines and anti-drug mAb are genetically engineered human or bacterial enzymes that metabolize drugs of abuse, lowering the concentration of free active drug. Pre-clinical and clinical data support development of effective biologics for SUD.
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页码:3005 / 3019
页数:15
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