Author: Caballero, Armando; Filgueira, Lázaro M; Betancourt, Julio; Sánchez, Naivy; Hidalgo, Carlos; RamÃrez, Alberto; Martinez, Alejandro; Despaigne, Rolando E; Escalona, Alberto; Diaz, Henrry; Meriño, Elio; Ortega, Lilia M; Castillo, Ulises; Ramos, Mayra; Saavedra, Danay; GarcÃa, Yanelda; Lorenzo, Geydi; Cepeda, Meylán; Arencibia, Maylén; Cabrera, Leticia; Domecq, Milagros; Estévez, Daymys; Valenzuela, Carmen; Lorenzo, Patricia; Sánchez, Lizet; Mazorra, Zaima; León, Kalet; Crombet, Tania
Title: Treatment of COVIDâ€19 patients with the antiâ€CD6 antibody itolizumab Cord-id: 3dxg3fhd Document date: 2020_11_25
ID: 3dxg3fhd
Snippet: OBJECTIVES: COVIDâ€19 can lead to a hyperinflammatory state. CD6 is a glycoprotein expressed on mature T lymphocytes which is a crucial regulator of the Tâ€cell activation. Itolizumab is a humanised antibody targeting CD6. Nonclinical and clinical data in autoimmune diseases indicate that it lowers multiple cytokines primarily involving the Th1/Th17 pathway. The primary objective of this study was to assess the impact of itolizumab in arresting the lung function deterioration of COVIDâ€19 pat
Document: OBJECTIVES: COVIDâ€19 can lead to a hyperinflammatory state. CD6 is a glycoprotein expressed on mature T lymphocytes which is a crucial regulator of the Tâ€cell activation. Itolizumab is a humanised antibody targeting CD6. Nonclinical and clinical data in autoimmune diseases indicate that it lowers multiple cytokines primarily involving the Th1/Th17 pathway. The primary objective of this study was to assess the impact of itolizumab in arresting the lung function deterioration of COVIDâ€19 patients. Secondary objectives included safety, duration of ventilation, 14â€day mortality and evaluation of interleukin 6 concentration. METHODS: Patients with confirmed SARSâ€CoVâ€2 received itolizumab in combination with other therapies included in the national protocol for COVIDâ€19. RESULTS: Seventy critical, severe or moderate patients were treated with itolizumab in 10 Cuban hospitals. Median age was 68, and 94% had comorbidities. After 72 h, most patients improved the PO(2)/FiO(2) ratio and reduced FiO2 requirements. Ventilation time was 8 days for critical and 1 day for severe cases. Ten patients had related adverse events while 3 subjects developed related serious events. In 30 patients, interleukin 6 decreased in individuals with high level and did not change in those with lower concentration. Fourteenâ€day lethality rate was 4% and 18% for moderate and severe patients, respectively. The proportion of moderate or severe patients with ventilation or death at day 14 was 9.8%. Time to treatment, neurological manifestations and biomarkers such as NLR were significantly associated with higher lethality. CONCLUSIONS: The opportune administration of itolizumab might interrupt the hyperinflammatory cascade and prevent COVIDâ€19 morbidity and mortality.
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