Selection, design, and engineering of therapeutic antibodies

被引:53
作者
Presta, LG [1 ]
机构
[1] Schering Plough Biopharma, Palo Alto, CA 94304 USA
关键词
antibody engineering; target selection; biologic therapeutics;
D O I
10.1016/j.jaci.2005.08.003
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
mAbs account for an increasing portion of marketed human biological therapeutics. As a consequence, the importance of optimal selection, design, and engineering of these not only has expanded in the past 2 decades but also is now coming into play as a competitive factor. This review delineates the 4 basic areas for optimal therapeutic antibody selection and provides examples of the increasing number of considerations necessary for, and options available for, antibody design. Though some of the advances in antibody technology (eg, antibodies derived from phage-display libraries) have already made it to market, other more recent advances, such as engineering antibodies for enhanced effector functions, may not be far behind, especially given the increasing competition for therapeutic antibodies to the same target (eg, anti-CD20 and anti-TNF-alpha).
引用
收藏
页码:731 / 736
页数:6
相关论文
共 52 条
  • [1] Adams GP, 2001, CANCER RES, V61, P4750
  • [2] A SINGLE AMINO-ACID SUBSTITUTION ABOLISHES THE HETEROGENEITY OF CHIMERIC MOUSE/HUMAN (IGG4) ANTIBODY
    ANGAL, S
    KING, DJ
    BODMER, MW
    TURNER, A
    LAWSON, ADG
    ROBERTS, G
    PEDLEY, B
    ADAIR, JR
    [J]. MOLECULAR IMMUNOLOGY, 1993, 30 (01) : 105 - 108
  • [3] Isomerization of an aspartic acid residue in the complementarity-determining regions of a recombinant antibody to human IgE: Identification and effect on binding affinity
    Cacia, J
    Keck, R
    Presta, LG
    Frenz, J
    [J]. BIOCHEMISTRY, 1996, 35 (06) : 1897 - 1903
  • [4] Bispecific human IgG by design
    Carter, P
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 2001, 248 (1-2) : 7 - 15
  • [5] HUMANIZATION OF AN ANTI-P185HER2 ANTIBODY FOR HUMAN CANCER-THERAPY
    CARTER, P
    PRESTA, L
    GORMAN, CM
    RIDGWAY, JBB
    HENNER, D
    WONG, WLT
    ROWLAND, AM
    KOTTS, C
    CARVER, ME
    SHEPARD, HM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (10) : 4285 - 4289
  • [6] The liberation of CD44
    Cichy, J
    Puré, E
    [J]. JOURNAL OF CELL BIOLOGY, 2003, 161 (05) : 839 - 843
  • [7] Stability improvement of antibodies for extracellular and intracellular applications:: CDR grafting to stable frameworks and structure-based framework engineering
    Ewert, S
    Honegger, A
    Plückthun, A
    [J]. METHODS, 2004, 34 (02) : 184 - 199
  • [8] Frederick L, 2000, CANCER RES, V60, P1383
  • [9] Structure of the Fc fragment of human IgE bound to its high-affinity receptor FcεRIα
    Garman, SC
    Wurzburg, BA
    Tarchevskaya, SS
    Kinet, JP
    Jardetzky, TS
    [J]. NATURE, 2000, 406 (6793) : 259 - 266
  • [10] Multiple roles for the major histocompatibility complex class I-related receptor FcRn
    Ghetie, V
    Ward, ES
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 2000, 18 : 739 - 766