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Differential Cytokine Responses in Hospitalized COVID-19 Patients Limit Efficacy of Remdesivir.
Chan, Yi-Hao; Young, Barnaby E; Fong, Siew-Wai; Ding, Ying; Goh, Yun Shan; Chee, Rhonda Sin-Ling; Tan, Seow-Yen; Kalimuddin, Shirin; Tambyah, Paul A; Leo, Yee-Sin; Ng, Lisa F P; Lye, David Chien; Renia, Laurent.
  • Chan YH; ASTAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science, Technology and Research, Singapore, Singapore.
  • Young BE; Singapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
  • Fong SW; National Centre for Infectious Diseases, Singapore, Singapore.
  • Ding Y; Department of Infectious Diseases, Tan Tock Seng Hospital, Singapore, Singapore.
  • Goh YS; Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore, Singapore.
  • Chee RS; ASTAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science, Technology and Research, Singapore, Singapore.
  • Tan SY; Singapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
  • Kalimuddin S; National Centre for Infectious Diseases, Singapore, Singapore.
  • Tambyah PA; ASTAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science, Technology and Research, Singapore, Singapore.
  • Leo YS; Singapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
  • Ng LFP; ASTAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science, Technology and Research, Singapore, Singapore.
  • Lye DC; Singapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
  • Renia L; Department of Infectious Diseases, Changi General Hospital, Singapore, Singapore.
Front Immunol ; 12: 680188, 2021.
Article in English | MEDLINE | ID: covidwho-1311374
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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Adenosine Monophosphate / Cytokines / Alanine / SARS-CoV-2 / COVID-19 Drug Treatment / Hospitalization Type of study: Cohort study / Observational study / Prognostic study Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: English Journal: Front Immunol Year: 2021 Document Type: Article Affiliation country: Fimmu.2021.680188

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Adenosine Monophosphate / Cytokines / Alanine / SARS-CoV-2 / COVID-19 Drug Treatment / Hospitalization Type of study: Cohort study / Observational study / Prognostic study Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: English Journal: Front Immunol Year: 2021 Document Type: Article Affiliation country: Fimmu.2021.680188