Improved Immunotoxins with Novel Functional Elements

被引:15
作者
Hetzel, C. [1 ]
Bachran, C. [2 ]
Tur, M. K. [3 ]
Fuchs, H. [2 ]
Stoecker, M. [3 ]
机构
[1] Fraunhofer IME, Dept Pharmaceut Prod Dev, D-52074 Aachen, Germany
[2] Charite, Zent Inst Lab Med & Pathobiochem, D-12200 Berlin, Germany
[3] Univ Hosp RWTH Aachen, Helmholtz Inst Biomed Engn, Chair Appl Med Engn, Dept Expt Med & Immunotherapy, D-52074 Aachen, Germany
关键词
RICIN-A-CHAIN; CELL-PENETRATING PEPTIDES; PROTEIN TRANSDUCTION DOMAINS; PSEUDOMONAS EXOTOXIN-A; ACUTE MYELOID-LEUKEMIA; PHASE-I TRIAL; FUSION PROTEIN; MONOCLONAL-ANTIBODY; DRUG-DELIVERY; PHOTOCHEMICAL INTERNALIZATION;
D O I
10.2174/138161209788923930
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Immunotoxins (ITs) are protein-based drugs combining a target-specific binding domain ( usually derived from an antibody) and a cytotoxic domain to kill target cells. They are among the most promising new therapeutic tools to fight cancer, and several clinical trials have been completed with encouraging results. Although the targeted elimination of malignant cells is an elegant concept, there are numerous practical challenges that limit the clinical use of ITs, including inefficient cellular uptake, low cytotoxicity and off-target effects. Here we present some of the strategies that have been developed to improve the efficacy of ITs, particularly those involving the incorporation of functional peptide sequences into recombinant ITs to improve target binding, modify plasma half life and distribution, boost tumor penetration, enhance cellular uptake and increase cytotoxic efficiency.
引用
收藏
页码:2700 / 2711
页数:12
相关论文
共 184 条
[1]
ADAMS GP, 1993, CANCER RES, V53, P4026
[2]
Prolonged in vivo tumour retention of a human diabody targeting the extracellular domain of human HER2/neu [J].
Adams, GP ;
Schier, R ;
McCall, AM ;
Crawford, RS ;
Wolf, EJ ;
Weiner, LM ;
Marks, JD .
BRITISH JOURNAL OF CANCER, 1998, 77 (09) :1405-1412
[3]
From combinatorial chemistry to cancer-targeting peptides [J].
Aina, Olulanu H. ;
Liu, Ruiwu ;
Sutcliffe, Julie L. ;
Marik, Jan ;
Pan, Chong-Xian ;
Lam, Kit S. .
MOLECULAR PHARMACEUTICS, 2007, 4 (05) :631-651
[4]
Humanization of antibodies [J].
Almagro, Juan C. ;
Fransson, Johan .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2008, 13 :1619-1633
[5]
Membrane interaction and perturbation mechanisms induced by two cationic cell penetrating peptides with distinct charge distribution [J].
Alves, Isabel D. ;
Goasdoue, Nicole ;
Correia, Isabelle ;
Aubry, Soline ;
Galanth, Cecile ;
Sagan, Sandrine ;
Lavielle, Solange ;
Chassaing, Gerard .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2008, 1780 (7-8) :948-959
[6]
A dimeric angiogenin immunofusion protein mediates selective toxicity towards CD22+ tumor cells [J].
Arndt, MAE ;
Krauss, J ;
Vu, BK ;
Newton, DL ;
Rybak, SM .
JOURNAL OF IMMUNOTHERAPY, 2005, 28 (03) :245-251
[7]
Conjugates of antisense oligonucleotides with the Tat and antennapedia cell-penetrating peptides: Effects on cellular uptake, binding to target sequences, and biologic actions [J].
Astriab-Fisher, A ;
Sergueev, D ;
Fisher, M ;
Shaw, BR ;
Juliano, RL .
PHARMACEUTICAL RESEARCH, 2002, 19 (06) :744-754
[8]
Regression of cutaneous tumor lesions in patients intratumorally injected with a recombinant single-chain antibody-toxin targeted to ErbB2/HER2 [J].
Azemar, M ;
Djahansouzi, S ;
Jäger, E ;
Solbach, C ;
Schmidt, M ;
Maurer, AB ;
Mross, K ;
Unger, C ;
von Minckwitz, G ;
Dall, P ;
Groner, B ;
Wels, WS .
BREAST CANCER RESEARCH AND TREATMENT, 2003, 82 (03) :155-164
[9]
The saponin-mediated enhanced uptake of targeted saporin-based drugs is strongly dependent on the saponin structure [J].
Bachran, C ;
Sutherland, M ;
Heisler, I ;
Hebestreit, P ;
Melzig, MF ;
Fuchs, H .
EXPERIMENTAL BIOLOGY AND MEDICINE, 2006, 231 (04) :412-420
[10]
Influence of protein transduction domains on target-specific chimeric proteins [J].
Bachran, C ;
Heisler, I ;
Fuchs, H ;
Sutherland, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 337 (02) :602-609