Development of monoclonal antibodies directed against cocaine and cocaethylene:: Potential new tools for immunotherapy

被引:7
作者
Danger, Y
Devys, A
Gadjou, C
Galons, H
Blanchard, D
Folléa, G
机构
[1] Etab Francais Sang, Biotechnol Lab, Nantes, France
[2] Univ Paris 05, Lab Chim Organ 2, Paris, France
来源
HYBRIDOMA AND HYBRIDOMICS | 2004年 / 23卷 / 04期
关键词
D O I
10.1089/1536859041651286
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cocaine abuse is a major health problem, with the number of overdose-related incidents on a constant increase. Monoclonal antibodies against cocaine and its major toxic metabolite cocaethylene, have been developed for immunotherapeutical neutralization in vivo. A series of monoclonal antibodies with high affinity for cocaethylene and cocaine were obtained. Clones DASm244-4D8A4A4 (4D8) and DASm244-5B3C3C6 (5B3) were selected and fully characterized. The antibodies secreted exhibited 1.40x10(8) and 3.69x10(7) M-1 affinity constants for [H-3]-cocaine and cocaethylene, respectively. In addition to cocaine, they bound to cocaethylene and did not recognize non-toxic cocaine metabolites. They did not bind to blood cells, indicating that they may be potential tools for cocaine neutralization in vivo in cases of overdose.
引用
收藏
页码:212 / 218
页数:7
相关论文
共 29 条
[1]  
Bosron W F, 1997, NIDA Res Monogr, V173, P27
[2]  
Brzezinski MR, 1997, DRUG METAB DISPOS, V25, P1089
[3]  
Bunny EB, 2001, J PHARMACOL EXP THER, V297, P696
[4]   Cocaine vaccines: Antibody protection against relapse in a rat model [J].
Carrera, MRA ;
Ashley, JA ;
Zhou, B ;
Wirsching, P ;
Koob, GF ;
Janda, KD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (11) :6202-6206
[5]   Venoms, antivenoms and immunotherapy [J].
Chippaux, JP ;
Goyffon, M .
TOXICON, 1998, 36 (06) :823-846
[6]  
ERLANGER BF, 1959, J BIOL CHEM, V234, P1090
[7]   A single dose of monoclonal anti-phencyclidine IgG offers long-term reductions in phencyclidine behavioral effects in rats [J].
Hardin, JS ;
Wessinger, WD ;
Wenger, GR ;
Proksch, JW ;
Laurenzana, EM ;
Owens, SM .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 302 (01) :119-126
[8]  
Hardin JS, 1998, J PHARMACOL EXP THER, V285, P1113
[9]   Metabolic consequences of drug misuse [J].
Henry, JA .
BRITISH JOURNAL OF ANAESTHESIA, 2000, 85 (01) :136-142
[10]   Evidence for opponent-process actions of intravenous cocaine and cocaethylene [J].
Knackstedt, LA ;
Samimi, MM ;
Ettenberg, A .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2002, 72 (04) :931-936