Abciximab: A new antiaggregant used in angioplasty

被引:21
作者
Genetta, TB
Mauro, VF
机构
[1] UNIV TOLEDO, COLL PHARM, TOLEDO, OH 43606 USA
[2] MED COLL OHIO, DEPT MED, TOLEDO, OH 43699 USA
[3] BALTIMORE VET AFFAIRS MED CTR, SERV PHARM, BALTIMORE, MD USA
关键词
D O I
10.1177/106002809603000309
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: TO review the scientific literature on the pharmacology and clinical uses of abciximab. DATA SOURCES: MEDLINE, Index Medicus and bibliographic literature searches of English-language articles pertaining to abciximab, 7E3, m7E3, and c7E3 were performed. Eli Lilly also provided unpublished results of the Evaluation of 7E3 for the Prevention of Ischemic Complications trial. DATA SELECTION: The selection of data presented focused on controlled trials using abciximab at doses currently approved by the Food and Drug Administration. DATA SYNTHESIS: Abciximab is a humanized chimeric Fab fragment of 7E3. 7E3 is a murine antibody directed against the integrin glycoprotein IIb/IIIa receptor (GPIIb/IIIa) located on platelets. These receptors play an integral part in platelet aggregation by allowing fibrinogen to bind to them and interconnect platelets. When administered intravenously, abciximab binds to GPIIb/IIIa and hinders platelet aggregation. Bleeding times and activated clotting times are increased and the platelets' response to adenosine diphosphate is reduced with the use of abciximab. Clinical trials have indicated that abciximab can reduce the incidence of abrupt closure and restenosis associated with percutaneous transluminal coronary angioplasty (PTCA) performed in high-risk patients. Clinical trials also suggest that abciximab may have a role in the treatment of unstable angina and the acute therapy of myocardial infarctions. Complications associated with abciximab include bleeding and thrombocytopenia. The thrombocytopenia is likely related to immunologic mechanisms. Zn addition, the production of antimurine antibodies has been demonstrated with abciximab use. Abciximab is currently approved for the prevention of abrupt coronary closure associated with PTCA in patients at high risk for this event. CONCLUSIONS: Abciximab is effective in preventing platelet aggregation and has been proven to be of clinical benefit in selected high-risk patients receiving PTCA.
引用
收藏
页码:251 / 257
页数:7
相关论文
共 28 条
[1]  
AGUIRRE F, 1993, CIRCULATION, V88, P252
[2]   THE USE OF ANTIBODIES IN CLINICAL CARDIOLOGY [J].
AZRIN, MA .
AMERICAN HEART JOURNAL, 1992, 124 (03) :753-768
[3]  
BENNETT JS, 1992, HOSP PRACT, V27, P124
[4]  
BHATTACHARYA S, 1991, CLIN RES, V39, pA196
[5]   EFFECTS OF PROFOUND PLATELET INHIBITION WITH C7E3 BEFORE CORONARY ANGIOPLASTY ON COMPLICATIONS OF CORONARY-BYPASS SURVEY [J].
BOEHRER, JD ;
KEREIAKES, DJ ;
NAVETTA, FI ;
CALIFF, RM ;
TOPOL, EJ .
AMERICAN JOURNAL OF CARDIOLOGY, 1994, 74 (11) :1166-1170
[6]  
BREZINA K, 1994, J INVASIVE CARDIOL, V6, pA38
[7]   USE OF A MONOCLONAL-ANTIBODY DIRECTED AGAINST THE PLATELET GLYCOPROTEIN IIB/IIIA RECEPTOR IN HIGH-RISK CORONARY ANGIOPLASTY [J].
CALIFF, RM ;
SHADOFF, N ;
VALETT, N ;
BATES, E ;
GALEANA, A ;
KNOPF, W ;
SHAFTEL, J ;
BENDER, MJ ;
AVERSANO, T ;
RAQUENO, J ;
GURBEL, P ;
COWFER, J ;
COHEN, M ;
CROSS, P ;
BITTL, J ;
EDDINGS, K ;
TAYLOR, M ;
DEROSA, K ;
HATTEL, L ;
COOPER, L ;
ESHELMAN, B ;
FINTEL, D ;
NIEMYSKI, P ;
KLEIN, L ;
KENNEDY, H ;
THORNTON, T ;
KEREIAKES, D ;
MARTIN, L ;
ANDERSON, L ;
HIGBY, N ;
ELLIS, S ;
BREZINA, K ;
GEORGE, B ;
CHAPEKIS, A ;
SMITH, D ;
ANWAR, A ;
GERBER, TL ;
PRITCHARD, GL ;
MYLER, R ;
SHAW, R ;
MURPHY, M ;
WARD, K ;
MADIGAN, NP ;
BLANKENSHIP, J ;
HALBERT, M ;
FLANAGAN, C ;
TANNENBAUM, M ;
POLICH, M ;
STEVENSON, C ;
TCHENG, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (14) :956-961
[8]   FLOW CYTOMETRIC OBSERVATIONS ON THE IN-VIVO USE OF FAB FRAGMENTS OF A CHIMERIC MONOCLONAL-ANTIBODY TO PLATELET GLYCOPROTEIN IIB-IIIA [J].
CHRISTOPOULOS, C ;
MACKIE, I ;
LAHIRI, A ;
MACHIN, S .
BLOOD COAGULATION & FIBRINOLYSIS, 1993, 4 (05) :729-737
[9]  
CHRISTOPOULOS C, 1994, CLIN EXP IMMUNOL, V98, P6
[10]   A NEW MURINE MONOCLONAL-ANTIBODY REPORTS AN ACTIVATION-DEPENDENT CHANGE IN THE CONFORMATION AND OR MICROENVIRONMENT OF THE PLATELET GLYCOPROTEIN IIB/IIIA COMPLEX [J].
COLLER, BS .
JOURNAL OF CLINICAL INVESTIGATION, 1985, 76 (01) :101-108