Differential Cytokine Responses in Hospitalized COVID-19 Patients Limit Efficacy of Remdesivir
Yi‐Hao Chana b c, Barnaby Edward Youngd e f, Siew‐Wai Fonga b c, Ying Dingf, Yun Shan Goha b c, Rhonda Sin‐Ling Cheea b c, Seow Yen Tang, Shirin Kalimuddinh i, Paul Anantharajah Tambyahj, Yee‐Sin Leod e f k l, Lisa F. P. Nga b c m n, David Chien Lyed e f l✉, Laurent Réniaa b c✉
- aASTAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science, Technology and Research, Singapore, Singapore
- bSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore
- cA*STAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science, Technology and Research, Singapore, Singapore
- dDepartment of Infectious Diseases, Tan Tock Seng Hospital, Singapore, Singapore
- eLee Kong Chian School of Medicine, Nanyang Technological University, Singapore, Singapore
- fNational Centre for Infectious Diseases, Singapore, Singapore
- gDepartment of Infectious Diseases, Changi General Hospital, Singapore, Singapore
- hDepartment of Infectious Diseases, Singapore General Hospital, Singapore, Singapore
- iEmerging Infectious Diseases Program, Duke-NUS Medical School, Singapore, Singapore
- jDepartment of Medicine, National University Hospital, Singapore, Singapore
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Abstract
A significant proportion of COVID-19 patients will progress to critical illness requiring invasive mechanical ventilation. This accentuates the need for a therapy that can reduce the severity of COVID-19. Clinical trials have shown the effectiveness of remdesivir in shortening recovery time and decreasing progression to respiratory failure and mechanical ventilation. However, some studies have highlighted its lack of efficacy in patients on high-flow oxygen and mechanical ventilation. This study uncovers some underlying immune response differences between responders and non-responders to remdesivir treatment. Immunological analyses revealed an upregulation of tissue repair factors BDNF, PDGF-BB and PIGF-1, as well as an increase in ratio of Th2-associated cytokine IL-4 to Th1-associated cytokine IFN-γ. Serological profiling of IgG subclasses corroborated this observation, with significantly higher magnitude of increase in Th2-associated IgG2 and IgG4 responses. These findings help to identify the mechanisms of immune regulation accompanying successful remdesivir treatment in severe COVID-19 patients.
TL;DRImmunological analyses revealed an upregulation of tissue repair factors BDNF, PDGF-BB and PIGF-1, as well as an increase in ratio of Th2- associated cytokine IL-4 to Th1-associated cytokine IFN-γ, which helps to identify the mechanisms of immune regulation accompanying successful remdesivir treatment in severe COVID-19 patients. (Semantic Scholar)

