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Updated: May 1, 2026

Analyzing Tumor and Tissue Distribution of Target Antigen Specific Therapeutic Antibody
Published on: May 16, 2020
Conditions of tumor-associated antigens as a proper target for therapeutic antibodies against solid cancers
1Institute for Comprehensive Medical Science, Fujita Health University , Toyoake, Aichi 470-1192, Japan.
Abstract:
Since the success of rituximab and trastuzumab for treatment of non-Hodgkin's lymphoma and breast cancer, respectively, a huge therapeutic potential of monoclonal antibodies (mAbs) was realized and development of therapeutic mAbs has been widely tried against various cancers. However, the successful examples are still limited and therapeutic mAbs are not yet available for the majority of human cancers. We established a procedure for comprehensive identification of tumor-associated antigens (TAAs) through the extensive isolation of human mAbs that may become therapeutic. Thirty-twoTAAs have been identified and 555 mAbs that bound to one of the TAAs have been isolated to date. Now we are trying to select TAAs as proper targets for therapy and candidate mAbs as drugs from among them. The immunohistochemical analysis using many fresh lung cancer specimens suggested probabilities of proper targets, and moreover, presence of cancer-specific epitopes that could be distinguished from normal epitopes on the same molecules by mAbs. For Abs to efficiently kill the cancer cells they should have the ability to induce immunological cytotoxicity such as ADCC and/or CDC. They should also be able to inhibit the function mediated by the target Ags. For clinical point of view, the continuous presence of the target molecule on the cell surface until cell death might be essential for successful treatment. Therefore, it will be required for targets TAAs to play essential roles in tumorigenesis. Otherwise the cancer cells that do not express them could selectively survive during treatment and finally become dominant. It was also suggested that even the same molecules could play different roles in tumorigenesis quite often in different patients. Therefore when we develop therapeutic Abs, we should obtain information about the conditions of patients including genetic background to whom the treatment will be effective. I will discuss how we can accomplish this purpose.
Insights
Researchers identified tumor-associated antigens (TAAs) and isolated human monoclonal antibodies (mAbs) for cancer therapy. They are selecting optimal TAAs and mAbs, considering patient genetics for effective cancer treatment.
Area of Science:
- Oncology
- Immunology
- Biotechnology
Background:
- Therapeutic monoclonal antibodies (mAbs) show promise in cancer treatment, building on successes like rituximab and trastuzumab.
- Despite potential, limited therapeutic mAbs are available for most human cancers, highlighting a need for new drug development.
Purpose of the Study:
- To establish a method for identifying tumor-associated antigens (TAAs) and isolating human mAbs for potential cancer therapeutics.
- To select promising TAAs and candidate mAbs for further development as anti-cancer drugs.
Main Methods:
- Comprehensive identification of TAAs through extensive isolation of human mAbs.
- Immunohistochemical analysis of lung cancer specimens to evaluate TAA target suitability and cancer-specific epitopes.
- Assessment of mAb-mediated immunological cytotoxicity (ADCC, CDC) and functional inhibition of target antigens.
Main Results:
- Identified 32 TAAs and isolated 555 mAbs targeting these antigens.
- Immunohistochemistry suggested potential targets and identified cancer-specific epitopes.
- Established criteria for selecting effective therapeutic mAbs, including induction of cytotoxicity and inhibition of target antigen function.
Conclusions:
- The study presents a strategy for developing therapeutic mAbs by identifying TAAs and candidate antibodies.
- Effective cancer therapy requires TAAs crucial for tumorigenesis and patient-specific considerations, including genetic background.
- Further research will focus on selecting optimal TAAs and mAbs, and tailoring treatments to individual patient profiles for maximum efficacy.
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