| Literature DB >> 27622021 |
Christine Sedlik1, Adèle Heitzmann1, Sophie Viel2, Rafik Ait Sarkouh3, Cornélie Batisse3, Frédéric Schmidt3, Philippe De La Rochere2, Nathalie Amzallag1, Eduardo Osinaga4, Pablo Oppezzo4, Otto Pritsch4, Xavier Sastre-Garau5, Pascale Hubert1, Sebastian Amigorena1, Eliane Piaggio1.
Abstract
Antibody-drug conjugates (ADC), combining the specificity of tumor recognition by monoclonal antibodies (mAb) and the powerful cytotoxicity of anticancer drugs, are currently under growing interest and development. Here, we studied the potential of Chi-Tn, a mAb directed to a glyco-peptidic tumor-associated antigen, to be used as an ADC for cancer treatment. First, we demonstrated that Chi-Tn specifically targeted tumor cells in vivo. Also, using flow cytometry and deconvolution microscopy, we showed that the Chi-Tn mAb is rapidly internalized - condition necessary to ensure the delivery of conjugated cytotoxic drugs in an active form, and targeted to early and recycling endosomes. When conjugated to saporin (SAP) or to auristatin F, the Chi-Tn ADC exhibited effective cytotoxicity to Tn-positive tumor cells in vitro, which correlated with the level of tumoral Tn expression. Furthermore, the Chi-Tn mAb conjugated to auristatin F also exhibited efficient antitumor activity in vivo, validating for the first time the use of an anti-Tn antibody as an effective ADC.Entities:
Keywords: Biodistribution; MMAF; Tn antigen; internalization; monoclonal antibody-drug conjugate
Year: 2016 PMID: 27622021 PMCID: PMC5006918 DOI: 10.1080/2162402X.2016.1171434
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110