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Clinical Cancer Research Vol. 9, 5454-5464, November 15, 2003
© 2003 American Association for Cancer Research


Review

Potentiation of Therapeutic Immune Responses against Malignancies with Monoclonal Antibodies

Oihana Murillo, Ainhoa Arina, Iñigo Tirapu, Carlos Alfaro, Guillermo Mazzolini, Belen Palencia, Ascensión López-Diaz De Cerio, Jesús Prieto, Maurizio Bendandi and Ignacio Melero

Centro de Investigación Médica aplicada and Clínica Universitaria, Universidad de Navarra, Pamplona, Spain

Immunotherapeutic monoclonal antibodies (mAbs) can be defined as those that exert their functions by tampering with immune system cell molecules, causing an enhancement of antitumor immune responses. Some of these antibodies are agonistic ligands for surface receptors involved in the activation of lymphocytes and/or antigen-presenting cells, whereas others are antagonists of mechanisms that normally limit the intensity of immune reactions. Several mAbs of this category have been described to display in vivo antitumor activity in mouse models. Only anti-CTLA-4 (CD152) mAb has entered clinical trials, but the preclinical effects described for anti-CD40, anti-CD137 (4-1BB), anti-CD102 (intercellular adhesion molecule-2), and regulatory T cell-depleting mAbs should lead to their prompt clinical development. Their use in combination with immunizations against tumor antigens has been reported to be endowed with synergistic properties. This new group of antitumor agents holds promise for at least additive effects with conventional therapies of cancer and deserves intensive translational research.




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Copyright © 2003 by the American Association for Cancer Research.