@misc{10818/48313,
year = {2017},
month = {8},
url = {http://hdl.handle.net/10818/48313},
abstract = {Currently it is well known that all biological drugs, including those with a fully human structure, are capable of inducing a host immune response known as immunogenicity [1]. The presence of ADAs can condition the drug´s level and action, thus modifying the therapeutic effect and even the safety profile by its mechanism of action - neutralizing or non-neutralizing - and / or an increase in its clearance. Immunogenicity is a dynamic factor to be taken into account in biological therapy, especially in long-term treatments, and as a relevant aspect in the assessment of secondary response loss [2]. With the above, not only the knowledge but also the management of the immunogenicity of the different biological treatments, represent a useful instrument for optimization of the strategies of use for each drug, and in the design of predictive models of response, which finally permits a significant improvement in the efficacy and safety profile, aiming to a personalization of the therapies, especially in patients with autoimmune diseases, genetic disorders and cancer [3]. This review summarizes the events of immunogenicity that produce the biological drug, the factor that influence to immunogenicity and the assessment of immunogenicity.},
publisher = {Current Protein and Peptide Science},
keywords = {Immunogenicity},
keywords = {Peptide},
keywords = {Biological drugs},
keywords = {Biosensor},
title = {Immunogenicity in protein and peptide based-therapeutics: An overview},
doi = {10.2174/1389203718666170828123449},
author = {Fernandez Rodriguez, Leonardo and Bustos, Helena and Garcia, Julio and Zapata, Carlos Daniel},
}