Antibody Drug Conjugate Bioinformatics: Drug Delivery through the Letterbox
Author(s) -
Dimitriοs Vlachakis,
Σοφία Κοσσίδα
Publication year - 2013
Publication title -
computational and mathematical methods in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.462
H-Index - 48
eISSN - 1748-6718
pISSN - 1748-670X
DOI - 10.1155/2013/282398
Subject(s) - drug , antibody , antibody drug conjugate , cancer immunotherapy , immune system , cytotoxic t cell , cancer , immunotherapy , immunology , drug delivery , biology , computational biology , monoclonal antibody , medicine , pharmacology , cancer research , chemistry , in vitro , genetics , organic chemistry
Antibodies appear to be the first line of defence in the adaptive immune response of vertebrates and thereby are involved in a multitude of biochemical mechanisms, such as regulation of infection, autoimmunity, and cancer. It goes without saying that a full understanding of antibody function is required for the development of novel antibody-interacting drugs. These drugs are the Antibody Drug Conjugates (ADCs), which are a new type of targeted therapy, used for example for cancer. They consist of an antibody (or antibody fragment such as a single-chain variable fragment [scFv]) linked to a payload drug (often cytotoxic). Because of the targeting, the side effects should be lower and give a wider therapeutic window. Overall, the underlying principle of ADCs is to discern the delivery of a drug that is cytotoxic to a target that is cancerous, hoping to increase the antitumoural potency of the original drug by reducing adverse effects and side effects, such as toxicity of the cancer target. This is a pioneering field that employs state-of-the-art computational and molecular biology methods in the fight against cancer using ADCs.
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