Dortmund, Germany and New Jersey USA, 31 March 2008: Tumor Necrosis Factor (TNF)-a inhibitors used to treat rheumatic diseases may bind to a significant number of proteins other than their main target, according to the results of an in vitro study published in Analytical and Bioanalytical Chemistry. This off-target binding activity might explain some of the side effects reported for these commonly used biotherapeutics.
Researchers from University Children’s Hospital Düsseldorf, Ruhr-University Bochum and Protagen AG used protein biochips to investigate the protein binding activity of three protein therapeutics for the treatment of Rheumatoid Arthritis and Juvenile Idiopathic Arthritis. Infliximab (Remicade®, Centocor) is a chimeric human and mouse antibody; Adalimumab (Humira®, Abbott) is a recombinant humanized monoclonal anti-TNF-a antibody; and Etanercept (Enbrel®, Amgen and Wyeth) is a fusion protein consisting of a TNF-a receptor and the Fc portion from a human IgG1 antibody.
Side effects of Infliximab include hypersensitivity and other symptoms such as fever, itching, difficulty in breathing and chest pain, which could be caused by the patient experiencing an immune reaction to the murine component of the antibody. The side-effects of the other two drugs include an increased risk of contracting serious infections, as well as other problems that could be the result of a treatment-induced autoimmune response.
The researchers incubated UNIchip® AV-400 protein biochips with the TNF-a blocking agents to check their respective specificity. Each set of protein biochips contained a printed serial dilution of naturally folded TNF-a and a random selection of 384 different recombinant human proteins. Though the concentration of drugs used in the experiment ensured that these all had the same level of TNF-a binding activity in vitro, the products showed severe differences in specificity.
Infliximab was the most specific antibody with no off-target activity detected. Both Etanercept and Adalimumab showed off-target activity, with Etanercept binding to 10 proteins with affinities greater than 20% of its binding affinity for TNF-a. Adalimumab bound 19 proteins other than TNF-a, though its affinity for these was lower, at only 12-18% of its affinity for TNF-a. Several of these proteins are involved in the assembly of ribosomes and protein synthesis.
The authors said: “TNF-a inhibitors have been shown to be highly efficient and clinically useful drugs for the treatment of rheumatic diseases. At the same time there are reports about adverse side effects associated with TNF-a inhibitor treatment. Although there is no direct evidence that the off-target activity we have seen leads to pathological consequences, this link cannot be excluded.”
Christoph Hüls, CEO of Protagen, the company that created the protein biochips used in this study said: “The results published today show how protein biochips, such as our UNIchip® products, could be highly useful in antibody development, as researchers can test the specificity of their therapeutic candidates. Those exhibiting the least off-target activity can then be taken forward to the next stage of development, as it is likely that these will cause fewer side effects when administered to patients. We believe that the power of quantitative analysis of off-target binding using biochips will mean that providing these data becomes a regulatory requirement for therapeutic antibody approval in the future.”
