Mechanisms of action of new drugs in PTCL. Two naked antibodies targeting the CD52 and CCR4 molecules (alemtuzumab and mogamulizumab, respectively) have shown interesting potency in PTCL by mediating antibody-dependent cell-mediated and complement-dependent cytotoxicity. Romidepsin is an HDAC, which is able, among other mechanisms, to restore expression of proapoptotic genes. Pralatrexate is a dihydrofolate reductase inhibitor that impedes DNA synthesis. BV is an ADC combining an anti-CD30 monoclonal antibody attached by a protease-cleavable linker to a cytotoxic agent, the MMAE. MMAE is released upon internalization by CD30-expressing cells and disrupts microtubule polymerization. HDAC, histone deacetylase inhibitor.

Mechanisms of action of new drugs in PTCL. Two naked antibodies targeting the CD52 and CCR4 molecules (alemtuzumab and mogamulizumab, respectively) have shown interesting potency in PTCL by mediating antibody-dependent cell-mediated and complement-dependent cytotoxicity. Romidepsin is an HDAC, which is able, among other mechanisms, to restore expression of proapoptotic genes. Pralatrexate is a dihydrofolate reductase inhibitor that impedes DNA synthesis. BV is an ADC combining an anti-CD30 monoclonal antibody attached by a protease-cleavable linker to a cytotoxic agent, the MMAE. MMAE is released upon internalization by CD30-expressing cells and disrupts microtubule polymerization. HDAC, histone deacetylase inhibitor.

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