Author:
Rotundo Salvatore,Borelli Massimo,Scaglione Vincenzo,Lionello Rosaria,Biamonte Flavia,Olivadese Vincenzo,Quirino Angela,Morrone Helen Linda,Matera Giovanni,Costanzo Francesco Saverio,Russo Alessandro,Trecarichi Enrico Maria,Torti Carlo,Serapide Francesca,Tassone Bruno,Fusco Paolo,Davoli Chiara,La Gamba Valentina,Morrone Helen Linda,Berardelli Lavinia,Tassone Maria Teresa,Serraino Riccardo,Costa Chiara,Foti Daniela Patrizia,Longhini Federico,Bruni Andrea,Garofalo Eugenio,Biamonte Eugenio,Laganà Domenico,Petullà Maria,Bertucci Bernardo,Barreca Giorgio Settimo,Giancotti Aida,Gallo Luigia,Lamberti Angelo,Liberto Maria Carla,Marascio Nadia,De Francesco Adele Emanuela,
Abstract
AbstractIn a convenience sample of 93 patients treated with monoclonal antibodies (moAbs) against SARS-CoV-2, the interleukin-62/lymphocyte count ratio (IL-62/LC) was able to predict clinical worsening both in early stages of COVID-19 and in oxygen-requiring patients. Moreover, we analysed 18 most at-risk patients with asymptomatic or mild disease treated with both moAbs and antiviral treatment and found that only 2 had clinical progression, while patients with a similar risk were reported to have an unfavourable outcome in most cases from recent data. In only one of our 18 patients, clinical progression was attributable to COVID-19, and in the other cases, clinical progression was observed despite IL-62/LC being above the risk cut-off. In conclusion, IL-62/LC may be a valuable method to identify patients requiring more aggressive treatments both in earlier and later stages of the disease; however, most at-risk patients can be protected from clinical worsening by combining moAbs and antivirals, even if levels of the IL-62/LC biomarker are lower than the risk cut-off.
Funder
Università degli studi "Magna Graecia" di Catanzaro
Publisher
Springer Science and Business Media LLC
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine