| Literature DB >> 30985099 |
Andrea Cruz1, Raquel Queirós1, Catarina M Abreu1,2, Catarina Barata1,3, Rosa Fernandes4,5, Rufino Silva4,6, Antonio F Ambrósio4,5, Ricardo Soares-Dos-Reis7,8,9, Joana Guimarães7,8,10, Maria José Sá7,11,12, João B Relvas13, Paulo P Freitas1, Inês Mendes Pinto1.
Abstract
Inflammation associated with cancer, neurodegenerative, ocular, and autoimmune diseases has a considerable impact on public health. Tumor necrosis factor alpha (TNFα) is a key mediator of inflammatory responses, responsible for many of the systemic manifestations during the inflammatory process. Thus, inhibition of TNFα is a commonplace practice in the treatment of these disorders. Successful therapy requires the ability to determine the appropriate dose of anti-TNFα drugs to be administered in a timely manner, based on circulating TNFα levels. In this Letter, we report the development of an immunosensor technology able to quantify TNFα at the picogram level in relevant human body fluids, holding the potential to early detect inflammation and monitor TNFα levels during treatment, enabling TNFα-targeted treatments to be tailored according to the immune status of an individual patient. This immunosensor technology is significantly more rapid and sensitive than conventional enzyme linked immunosorbent assays, maintaining high specificity and requiring small sample volumes. These features might also be advantageous in the context of personalized medicine, as this analytical platform can deliver advanced diagnostics and reduce clinical burden.Entities:
Keywords: Electrochemical immunosensor; TNFα; human CSF; human blood serum; human tears; inflammation monitoring
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Year: 2019 PMID: 30985099 DOI: 10.1021/acschemneuro.9b00036
Source DB: PubMed Journal: ACS Chem Neurosci ISSN: 1948-7193 Impact factor: 4.418