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Published on: June 28, 2021
Development of a new high-affinity human antibody with antitumor activity against solid and blood malignancies
Mouldy Sioud1, Phuong Westby1, Vlada Vasovic2
1Department of Cancer Immunology, Rikshospitalet-Radiumhospitalet, University Hospital, Oslo, Norway.
Abstract:
mAbs have emerged as a promising strategy for the treatment of cancer. However, in several malignancies, no effective antitumor mAbs are yet available. Identifying therapeutic mAbs that recognize common tumor antigens could render the treatment widely applicable. Here, a human single-chain variable fragment (scFv) antibody library was sequentially affinity selected against a panel of human cancer cell lines and an antibody fragment (named MS5) that bound to solid and blood cancer cells was identified. The MS5 scFv was fused to the human IgG1 Fc domain to generate an antibody (MS5-Fc fusion) that induced antibody-dependent cellular cytotoxicity and phagocytosis of cancer cells by macrophages. In addition, the MS5-Fc antibody bound to primary leukemia cells and induced antibody-dependent cellular cytotoxicity. In the majority of analyzed cancer cells, the MS5-Fc antibody induced cell surface redistribution of the receptor complexes, but not internalization, thus maximizing the accessibility of the IgG1 Fc domain to immune effector cells. In vitro stability studies showed that the MS5-Fc antibody was stable after 6 d of incubation in human serum, retaining ∼60% of its initial intact form. After intravenous injections, the antibody localized into tumor tissues and inhibited the growth of 3 different human tumor xenografts (breast, lymphoma, and leukemia). These antitumor effects were associated with tumor infiltration by macrophages and NK cells. In the Ramos B-cell lymphoma xenograft model, the MS5-Fc antibody exhibited a comparable antitumor effect as rituximab, a chimeric anti-CD20 IgG1 mAb. These results indicate that human antibodies with pan-cancer abilities can be generated from phage display libraries, and that the engineered MS5-Fc antibody could be an attractive agent for further clinical investigation.-Sioud, M., Westby, P., Vasovic, V., Fløisand, Y., Peng, Q. Development of a new high-affinity human antibody with antitumor activity against solid and blood malignancies.
Insights
Researchers developed a novel human antibody, MS5-Fc, demonstrating broad antitumor activity against solid and blood cancers. This pan-cancer antibody shows promise for widespread clinical application in oncology.
Area of Science:
- Oncology
- Immunology
- Biotechnology
Background:
- Monoclonal antibodies (mAbs) are a promising cancer treatment strategy.
- Effective antitumor mAbs are lacking for several malignancies.
- Identifying broadly applicable mAbs targeting common tumor antigens is crucial.
Purpose of the Study:
- To develop a novel human antibody with broad antitumor activity.
- To evaluate the efficacy and stability of the engineered antibody in preclinical models.
Main Methods:
- A human single-chain variable fragment (scFv) library was used for affinity selection.
- An antibody fragment (MS5) was identified and engineered into an MS5-Fc fusion protein.
- In vitro and in vivo studies assessed antibody binding, cytotoxicity, stability, and antitumor effects in xenograft models.
Main Results:
- The MS5-Fc antibody demonstrated binding to solid and blood cancer cells, inducing antibody-dependent cellular cytotoxicity (ADCC) and phagocytosis.
- MS5-Fc showed stability in human serum and localized to tumor tissues, inhibiting the growth of breast, lymphoma, and leukemia xenografts.
- Antitumor effects were linked to macrophage and NK cell infiltration, with comparable efficacy to rituximab in a lymphoma model.
Conclusions:
- Human antibodies with pan-cancer capabilities can be generated using phage display libraries.
- The engineered MS5-Fc antibody exhibits significant antitumor activity and warrants further clinical investigation for various malignancies.
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