Expanding the Targets Available to Therapeutic Antibodies via Novel Disease-specific Markers

被引:5
|
作者
Weidanz, Jon A. [1 ,2 ]
Hildebrand, William H. [3 ]
机构
[1] Texas Tech Univ, Hlth Sci Ctr, Dept Biomed Sci, Sch Pharm, Abilene, TX 79601 USA
[2] Texas Tech Univ, Hlth Sci Ctr, Ctr Immunotherapeut Res, Abilene, TX 79601 USA
[3] Univ Oklahoma, Hlth Sci Ctr, Dept Microbiol & Immunol, Oklahoma City, OK 73190 USA
关键词
T cell receptor mimics (TCRms); monoclonal antibodies (mAbs); Human Leukocyte Antigen (HLA); Major Histocompatibility Complex (MHC); epitope discovery; cancer therapy; immunotherapy; infectious disease therapy; mass spectrometry; CDC; ADCC; COMPLEX-RESTRICTED SPECIFICITY; HUMAN RECOMBINANT ANTIBODIES; TUMOR-ASSOCIATED ANTIGEN; CLASS-I COMPLEX; BREAST-CANCER; METASTATIC MELANOMA; MONOCLONAL-ANTIBODY; PEPTIDE EPITOPES; T-LYMPHOCYTES; CELLS;
D O I
10.3109/08830185.2011.608136
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The development of immunotherapies offers significant promise for clinical applications in cancer and infectious diseases. Here the authors describe a novel, integrated approach to immunotherapy that combines novel technologies to discover and target disease-specific peptide/HLA class I complexes. This unique class of markers makes the entire proteome accessible to antibody reagents and offers unsurpassed specificity for targeting cancerous and infected cells. Arm one of the three-armed approach uses an innovative technology for the efficient, direct discovery of new peptide/HLA class I markers. Arm two applies a powerful and inventive strategy to generate T-cell receptor mimics (TCRms), which are antibodies with exquisite binding specificity for peptide/HLA class I markers, and uses TCRms to validate the specific expression of markers on cancerous and infected cells. The third arm uses TCRms to target and kill diseased cells with high sensitivity and specificity. In summary, the combination of two pioneering technologies expands the repertoire of disease-specific markers that can be targeted by therapeutic antibodies and enables a powerful, integrated approach to HLA-based immunotherapy.
引用
收藏
页码:312 / 327
页数:16
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