From XenoMouse technology to panitumumab, the first fully human antibody product from transgenic mice

被引:139
作者
Jakobovits, Aya
Amad, Rafael G.
Yang, Xiaodong
RoskoS, Lorin
Schwab, Gisela
机构
[1] Agensys Inc, Santa Monica, CA 90404 USA
[2] Amgen Inc, Thousand Oaks, CA 91320 USA
[3] Intradigm Corp, Palo Alto, CA 94303 USA
[4] AstraZeneca Pharmaceut LP, Hayward, CA 94545 USA
[5] Exelixis Inc, San Francisco, CA 94083 USA
关键词
D O I
10.1038/nbt1337
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Therapeutic monoclonal antibodies have shown limited efficacy and safety owing to immunogenicity of mouse sequences in humans. Among the approaches developed to overcome these hurdles were transgenic mice genetically engineered with a 'humanized' humoral immune system. One such transgenic system, the XenoMouse, has succeeded in recapitulating the human antibody response in mice, by introducing nearly the entire human immunoglobulin loci into the germ line of mice with inactivated mouse antibody machinery. XenoMouse strains have been used to generate numerous high-affinity, fully human antibodies to targets in multiple disease indications, many of which are progressing in clinical development. However, validation of the technology has awaited the recent regulatory approval of panitumumab (Vectibix), a fully human antibody directed against epidermal growth factor receptor (EGFR), as treatment for people with advanced colorectal cancer. The successful development of panitumumab represents a milestone for mice engineered with a human humoral immune system and their future applications.
引用
收藏
页码:1134 / 1143
页数:10
相关论文
共 84 条
[11]   Cetuximab shows activity in colorectal cancer patients with tumors that do not express the epidermal growth factor receptor by immunohistochemistry [J].
Chung, KY ;
Shia, J ;
Kemeny, NE ;
Shah, M ;
Schwartz, GK ;
Tse, A ;
Hamilton, A ;
Pan, D ;
Schrag, D ;
Schwartz, L ;
Klimstra, DS ;
Fridman, D ;
Kelsen, DP ;
Saltz, LB .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (09) :1803-1810
[12]   Combination therapy enhances the inhibition of tumor growth with the fully human anti-type 1 insulin-like growth factor receptor monoclonal antibody CP-751,871 [J].
Cohen, BD ;
Baker, DA ;
Soderstrom, C ;
Tkalcevic, G ;
Rossi, AM ;
Miller, PE ;
Tengowski, MW ;
Wang, F ;
Gualberto, A ;
Beebe, JS ;
Moyer, JD .
CLINICAL CANCER RESEARCH, 2005, 11 (05) :2063-2073
[13]   THE HUMAN-IMMUNOGLOBULIN V-H REPERTOIRE [J].
COOK, GP ;
TOMLINSON, IM .
IMMUNOLOGY TODAY, 1995, 16 (05) :237-242
[14]   Cetuximab monotherapy and cetuximab plus irinotecan in irinotecan-refractory metastatic colorectal cancer [J].
Cunningham, D ;
Humblet, Y ;
Siena, S ;
Khayat, D ;
Bleiberg, H ;
Santoro, A ;
Bets, D ;
Mueser, M ;
Harstrick, A ;
Verslype, C ;
Chau, I ;
Van Cutsem, E .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (04) :337-345
[15]   SEQUENCING THE ERBA GENE OF AVIAN ERYTHROBLASTOSIS VIRUS REVEALS A NEW TYPE OF ONCOGENE [J].
DEBUIRE, B ;
HENRY, C ;
BENAISSA, M ;
BISERTE, G ;
CLAVERIE, JM ;
SAULE, S ;
MARTIN, P ;
STEHELIN, D .
SCIENCE, 1984, 224 (4656) :1456-1459
[16]   SIGNAL TRANSDUCTION BY EPIDERMAL GROWTH-FACTOR OCCURS THROUGH THE SUBCLASS OF HIGH-AFFINITY RECEPTORS [J].
DEFIZE, LHK ;
BOONSTRA, J ;
MEISENHELDER, J ;
KRUIJER, W ;
TERTOOLEN, LGJ ;
TILLY, BC ;
HUNTER, T ;
HENEGOUWEN, PMPV ;
MOOLENAAR, WH ;
DELAAT, SW .
JOURNAL OF CELL BIOLOGY, 1989, 109 (05) :2495-2507
[17]   ErbB-3 mediates phosphoinositide 3-kinase activity in gefitinib-sensitive non-small cell lung cancer cell lines [J].
Engelman, JA ;
Jänne, PA ;
Mermel, C ;
Pearlberg, J ;
Mukohara, T ;
Fleet, C ;
Cichowski, K ;
Johnson, BE ;
Cantley, LC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (10) :3788-3793
[18]   High-avidity human IgG kappa monoclonal antibodies from a novel strain of minilocus transgenic mice [J].
Fishwild, DM ;
ODonnell, SL ;
Bengoechea, T ;
Hudson, DV ;
Harding, F ;
Bernhard, SL ;
Jones, D ;
Kay, RM ;
Higgins, KM ;
Schramm, SR ;
Lonberg, N .
NATURE BIOTECHNOLOGY, 1996, 14 (07) :845-851
[19]  
FOLTZ IN, 2006, DRUGS, V66, P2005
[20]  
Ford Shirin Khambata, 2006, Proceedings of the American Association for Cancer Research Annual Meeting, V47, P950