Claudin-targeted drug development using anti-claudin monoclonal antibodies to treat hepatitis and cancer
- Ann N Y Acad Sci. 2017 Jun;1397(1):5-16. doi: 10.1111/nyas.13337.
- 1. Graduate School of Pharmaceutical Sciences, Osaka University, Suita, Osaka, Japan.
- 2. Department of Biochemistry and Cell Biology, National Institute of Infectious Diseases, Tokyo, Japan.
- 3. Department of Molecular Pathology, Nara Medical University, Nara, Japan.
The 27-member family of tetraspan membrane proteins known as claudins (CLDNs) is a major component of tight junctions. A series of studies elucidating the relationship between CLDNs and various pathological conditions has provided new insights into drug development. For instance, CLDN-1 may be a potent target for epidermal absorption of drugs and for treating hepatitis C virus (HCV) Infection. CLDN-4 may be a target for treating Cancer. Because CLDNs are also expressed in various normal tissues, safety and efficacy evaluations are critical for translational research. We previously developed several anti-CLDN antibodies and have established proof of concept for CLDN-targeted drug development using these reagents. Here, we provide an overview of CLDN-1 as a target for improving epidermal drug absorption and preventing HCV Infection and of CLDN-4 as a target for Anticancer therapeutics.
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