Efalizumab: An overview

被引:57
作者
Leonardi, CL [1 ]
机构
[1] St Louis Univ, Sch Med, Dept Dermatol, St Louis, MO 63110 USA
关键词
D O I
10.1016/S0190-9622(03)01141-1
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Efalizumab (anti-CD11a), a targeted T cell modulator, is a humanized monoclonal antibody being studied for plaque psoriasis. Phase I and II studies demonstrated that efalizumab treatment results in histologic improvement and clinical benefit in patients with moderate to severe disease. Phase III clinical trials confirmed the clinical activity and safety of weekly efalizumab. Efalizumab is associated with a rapid onset of clinical benefit, with significant improvements observed as early as 4 weeks. Extending treatment from 12 to 24 weeks both maintains and improves the initial responses achieved at 12 weeks. Both 12 and 24 weeks of efalizumab therapy were generally well tolerated. Ongoing studies are being conducted to further define the optimal dosing and administration schedules for efalizumab in patients with moderate to severe plaque psoriasis.
引用
收藏
页码:S98 / S104
页数:7
相关论文
共 21 条
[1]   ERYTHRODERMIC PSORIASIS - PRECIPITATING FACTORS, COURSE, AND PROGNOSIS IN 50 PATIENTS [J].
BOYD, AS ;
MENTER, A .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1989, 21 (05) :985-991
[2]   DERMATOLOGY LIFE QUALITY INDEX (DLQI) - A SIMPLE PRACTICAL MEASURE FOR ROUTINE CLINICAL USE [J].
FINLAY, AY ;
KHAN, GK .
CLINICAL AND EXPERIMENTAL DERMATOLOGY, 1994, 19 (03) :210-216
[3]   Effects of administration of a single dose of a humanized monoclonal antibody to CD11a on the immunobiology and clinical activity of psoriasis [J].
Gottlieb, A ;
Krueger, JG ;
Bright, R ;
Ling, M ;
Lebwohl, M ;
Kang, S ;
Feldman, S ;
Spellman, M ;
Wittkowski, K ;
Ochs, HD ;
Jardieu, P ;
Bauer, R ;
White, M ;
Dedrick, R ;
Garovoy, M .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2000, 42 (03) :428-435
[4]  
GOTTLIEB A, 2002, 60 ANN M AM AC DERM
[5]   Psoriasis as a model for T-cell-mediated disease - Immunobiologic and clinical effects of treatment with multiple doses of efalizumab, an anti-CD11a antibody [J].
Gottlieb, AB ;
Krueger, JG ;
Wittkowski, K ;
Dedrick, R ;
Walicke, PA ;
Garovoy, M .
ARCHIVES OF DERMATOLOGY, 2002, 138 (05) :591-600
[6]  
GOTTLIEB AB, 1999, ANN M SOC INV DERM M
[7]   RESPONSE OF PSORIASIS TO A LYMPHOCYTE-SELECTIVE TOXIN (DAB(389)IL-2) SUGGESTS A PRIMARY IMMUNE, BUT NOT KERATINOCYTE, PATHOGENIC BASIS [J].
GOTTLIEB, SL ;
GILLEAUDEAU, P ;
JOHNSON, R ;
ESTES, L ;
WOODWORTH, TG ;
GOTTLIEB, AB ;
KRUEGER, JG .
NATURE MEDICINE, 1995, 1 (05) :442-447
[8]   The Immunological Synapse: A Molecular Machine Controlling T Cell Activation [J].
Grakoui, Arash ;
Bromley, Shannon K. ;
Sumen, Cenk ;
Davis, Mark M. ;
Shaw, Andrey S. ;
Allen, Paul M. ;
Dustin, Michael L. .
JOURNAL OF IMMUNOLOGY, 2015, 194 (09) :221-227
[9]   Anti-CD11a treatment for psoriasis concurrently increases circulating T-cells and decreases plaque T-cells, consistent with inhibition of cutaneous T-cell trafficking [J].
Krueger, J ;
Gottlieb, A ;
Miller, B ;
Dedrick, R ;
Garovoy, M ;
Walicke, P .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2000, 115 (02) :333-333
[10]   The immunologic basis for the treatment of psoriasis with new biologic agents [J].
Krueger, JG .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2002, 46 (01) :1-23