BASE10 collaborates with DNA Link on Covid-19 antibody test project

27 November 2020 (Last Updated November 27th, 2020 10:20)

US-based BASE10 Genetics has collaborated with Korean firm DNA Link on a research project to analyse the usability of the latter’s antibody test, AccuFind COVID-19 IgG, in a healthcare setting.

BASE10 collaborates with DNA Link on Covid-19 antibody test project
DNA Link and BASE10 plan to launch the study in December. Credit: fernando zhiminaicela from Pixabay.

US-based BASE10 Genetics has collaborated with Korean firm DNA Link on a research project to analyse the usability of the latter’s antibody test, AccuFind COVID-19 IgG, in a healthcare setting.

Even though Covid-19 deaths and new confirmed cases continue to be on the higher side across nursing homes in the US, many infected people are recovering.

This indicates the potential in the link between antibodies and its protective properties either generated by prior exposure to Covid-19 or by a vaccine, once available.

Currently, most antibody tests on the market need the samples sent to a laboratory for evaluation.

This not only needs extra cost but also time, constraining population-wide studies of SARS-CoV-2 antibodies.

The study intends to expand access to antibody testing outside of laboratory settings.

BASE10 CEO Dr Michael Fang said: “An antibody test that can be done at the point of care without the need for a lab can more quickly provide information clinicians and administrators need to make decisions for their nursing home patients and staff.”

DNA Link and BASE10 plan to launch the study in December.

BASE10 Innovation vice-president Elizabeth Freund said: “DNA Link’s AccuFind performs very well in laboratory settings. The next logical step is to test its performance when used by healthcare professionals outside the lab.

“Many factors have the potential to affect test performance in lesser controlled settings so it’s an ambitious goal to be sure.

“However, if FDA believes the data demonstrates its safety and effectiveness under these conditions, we’ll be one step closer to FDA emergency use authorisation for point of care use.”