| Literature DB >> 26137403 |
Aitziber Buqué1, Norma Bloy2, Fernando Aranda3, Francesca Castoldi4, Alexander Eggermont5, Isabelle Cremer6, Wolf Hervé Fridman7, Jitka Fucikova8, Jérôme Galon9, Aurélien Marabelle10, Radek Spisek11, Eric Tartour12, Laurence Zitvogel10, Guido Kroemer13, Lorenzo Galluzzi14.
Abstract
Immunomodulatory monoclonal antibodies (mAbs) differ from their tumor-targeting counterparts because they exert therapeutic effects by directly interacting with soluble or (most often) cellular components of the immune system. Besides holding promise for the treatment of autoimmune and inflammatory disorders, immunomodulatory mAbs have recently been shown to constitute a potent therapeutic weapon against neoplastic conditions. One class of immunomodulatory mAbs operates by inhibiting safeguard systems that are frequently harnessed by cancer cells to establish immunological tolerance, the so-called "immune checkpoints." No less than 3 checkpoint-blocking mAbs have been approved worldwide for use in oncological indications, 2 of which during the past 12 months. These molecules not only mediate single-agent clinical activity in patients affected by specific neoplasms, but also significantly boost the efficacy of several anticancer chemo-, radio- or immunotherapies. Here, we summarize recent advances in the development of checkpoint-blocking mAbs, as well as of immunomodulatory mAbs with distinct mechanisms of action.Entities:
Keywords: CRC, colorectal carcinoma; CTLA4, cytotoxic T lymphocyte-associated protein 4; FDA, Food and Drug Administration; IL, interleukin; KIR, killer cell immunoglobulin-like receptor; MEDI4736; MPDL3280A; NK, natural killer; NSCLC, non-small cell lung carcinoma; PD-1, programmed cell death 1; RCC, renal cell carcinoma; TGFβ1, transforming growth factor β1; TLR, Toll-like receptor; TNFRSF, tumor necrosis factor receptor superfamily; Treg, regulatory T cell; ipilimumab; mAb, monoclonal antibody; nivolumab; pembrolizumab; urelumab
Year: 2015 PMID: 26137403 PMCID: PMC4485728 DOI: 10.1080/2162402X.2015.1008814
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110