Role of antibody-dependent cell-mediated cytotoxicity in the efficacy of therapeutic anti-cancer monoclonal antibodies

被引:170
作者
Iannello, A
Ahmad, A [1 ]
机构
[1] Univ Montreal, St Justine Hosp, Res Ctr, Montreal, PQ H3C 3J7, Canada
[2] Univ Montreal, Dept Microbiol & Immunol, Montreal, PQ H3C 3J7, Canada
关键词
ADCC; cancer; CD16; CD32; CD64; CD89; macrophages; monoclonal antibodies; neutrophils; NK cells; Fc receptors;
D O I
10.1007/s10555-005-6192-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In recent years, interest in anti-cancer therapeutic monoclonal antibodies (mAb) has been renewed. Several of these reagents have been approved for therapy in a variety of cancer patients and many others are in different stages of development. It is believed that multiple mechanisms are involved in the anti-cancer effects of these reagents. However, several in vitro and in vivo studies have demonstrated that antibody-dependent cell-mediated cytotoxicity (ADCC) is their predominant mode of action against cancer cells. The requirement for a direct interaction between mAb and receptors for the Fc region of the antibodies (FcR) has been demonstrated for anti-tumor effects of these antibodies. Consequently, FcR-bearing immune effector cells play an important role in mediating their effects. It is not surprising that cancer cells have developed different strategies to evade these antibodies. Several strategies are proposed to potentiate the mAb-mediated ADCC in cancer patients. They may enhance anti-cancer therapeutic effects of these regents.
引用
收藏
页码:487 / 499
页数:13
相关论文
共 83 条
[1]   Antibody-dependent cellular cytotoxicity in HIV infections [J].
Ahmad, A ;
Menezes, J .
FASEB JOURNAL, 1996, 10 (02) :258-266
[2]   HIV's evasion of host's NK cell response and novel ways of its countering and boosting Anti-HIV immunity [J].
Ahmad, A ;
Ahmad, R .
CURRENT HIV RESEARCH, 2003, 1 (03) :295-307
[3]   Evidence for a correlation between antibody-dependent cellular cytotoxicity-mediating Anti-HIV-1 antibodies and prognostic predictors of HIV infection [J].
Ahmad, R ;
Sindhu, STAK ;
Toma, E ;
Morisset, R ;
Vincelette, J ;
Menezes, J ;
Ahmad, A .
JOURNAL OF CLINICAL IMMUNOLOGY, 2001, 21 (03) :227-233
[4]   Human natural killer cell receptors and co-receptors [J].
Biassoni, R ;
Cantoni, C ;
Pende, D ;
Sivori, S ;
Parolini, S ;
Vitale, M ;
Bottino, C ;
Moretta, A .
IMMUNOLOGICAL REVIEWS, 2001, 181 :203-214
[5]   Human macrophages kill human mesangial cells by Fas-L-induced apoptosis when triggered by antibody via CD16 [J].
Boyle, JJ .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2004, 137 (03) :529-537
[6]  
Carson WE, 2001, EUR J IMMUNOL, V31, P3016, DOI 10.1002/1521-4141(2001010)31:10<3016::AID-IMMU3016>3.0.CO
[7]  
2-J
[8]   Improving the efficacy of antibody-based cancer therapies [J].
Carter, P .
NATURE REVIEWS CANCER, 2001, 1 (02) :118-129
[9]   HUMANIZATION OF AN ANTI-P185HER2 ANTIBODY FOR HUMAN CANCER-THERAPY [J].
CARTER, P ;
PRESTA, L ;
GORMAN, CM ;
RIDGWAY, JBB ;
HENNER, D ;
WONG, WLT ;
ROWLAND, AM ;
KOTTS, C ;
CARVER, ME ;
SHEPARD, HM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (10) :4285-4289
[10]   Therapeutic activity of humanized anti-CD20 monoclonal antibody and polymorphism in IgG Fc receptor FcγRIIIa gene [J].
Cartron, G ;
Dacheux, L ;
Salles, G ;
Solal-Celigny, P ;
Bardos, P ;
Colombat, P ;
Watier, H .
BLOOD, 2002, 99 (03) :754-758