Tests to Detect Common Immune Signature in Blood of COVID-19 Patients Could Predict Severity of Disease

Among several molecules expressed at atypical levels in the blood of patients, the researchers identified three in particular that could indicate how the disease will progress - what the researchers are calling the “triad”, made up of IP-10, interleukin-10 and interleukin-6. Patients with COVID-19 who displayed measurably higher levels of these molecules when first admitted to hospital went on to become more severely ill. The triad was found to be a more rigorous predictor of disease severity than commonly-used clinical indicators, including C-reactive protein (CRP), D-dimer or ferritin.

In addition, they found that within their patient cohort, measuring levels of IP-10 in blood taken on the first day in hospital was the most accurate way to date of predicting how long the patient would remain in hospital. The researchers are now looking to new collaborators to help develop robust, easily applied tests for these molecules. Since their preliminary analysis carried out in May, the team has now compared the immune signatures of COVID-19 patients with 10 age-matched patients who had non-COVID-19 lower respiratory tract infections. They found that high levels of the triad were not seen in those patients, suggesting this feature, in combination with other traits, may form a core COVID-19 immune signature. As well as continuing to monitor the immune response of patients in hospital, the team are also using these blood samples to gain further insights into the disease and are part of PHOSP (Post-HOSPitalisation COVID-19 study), a national consortium working to understand and improve long-term health outcomes for patients who were hospitalized with COVID-19.

“As we approach the upcoming winter flu season, along with the threat of resurgent cases of COVID-19, it is possible that our hospitals will come under great pressure. To handle this, we need to equip our doctors with the tools to make informed judgements about which patients are likely to improve and who might need more urgent care,” said Project lead Adrian Hayday, who heads the Crick’s Immunosurveillance Laboratory and is Professor of Immunobiology at King’s College London.

Related Links:

Francis Crick Institute
King’s College London
Guy's and St Thomas' NHS Foundation Trust