4.3 Article

Efficacy and safety evaluation of claudin-4-targeted antitumor therapy using a human and mouse cross-reactive monoclonal antibody

Journal

PHARMACOLOGY RESEARCH & PERSPECTIVES
Volume 4, Issue 5, Pages -

Publisher

JOHN WILEY & SONS LTD
DOI: 10.1002/prp2.266

Keywords

Cancer therapy; claudin; efficacy; monoclonal antibody; safety

Funding

  1. Health and Labour Sciences Research Grant from the Ministry of Health, Labour and Welfare of Japan
  2. Ministry of Education, Culture, Sports, Science and Technology of Japan [24390042]
  3. Adaptable and Seamless Technology Transfer Program through Target-driven R&D, Japan Science and Technology Agency
  4. Platform for Drug Discovery, Informatics, and Structural Life Science from the Ministry of Education, Culture, Sports, Science and Technology, Japan
  5. Takeda Science Foundation
  6. Advanced Research for Medical Products Mining Program of the National Institute of Biomedical Innovation (NIBIO)
  7. Grants-in-Aid for Scientific Research [26293014, 24390042, 16H05164] Funding Source: KAKEN

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Claudin-4 (CLDN-4), a tight-junction protein, is overexpressed in various malignant tumors, including gastric, colorectal, pancreatic, and breast cancers. However, CLDN-4 is also expressed in normal tissues, including the liver, pancreas, kidney, and small intestine. Whether CLDN-4 is an effective and safe target for cancer therapy has been unclear owing to the lack of a binder with both CLDN-4 specificity and cross-reactivity to human and murine cells. In this study, we successfully generated a rat anti-CLDN-4 monoclonal antibody (5D12) that was specific to, and cross-reactive with, human and mouse CLDN-4. 5D12 recognized the second extracellular domain of human CLDN-4 in a conformation-dependent manner. A human-rat chimeric IgG1 of 5D12 (xi-5D12) activated the Fc gamma IIIa receptor, indicating the activation of antibodydependent cellular cytotoxicity in CLDN-4-expressing cells. Moreover, xi-5D12 significantly suppressed tumor growth in mice bearing human colorectal and gastric tumors without apparent adverse effects, such as weight loss or liver and kidney damage. These results suggest that CLDN-4 is a potent target for cancer therapy and that an anti-CLDN-4 antibody is a promising candidate anticancer agent.

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