Differential Cytokine Responses in Hospitalized COVID-19 Patients Limit Efficacy of Remdesivir

被引:8
|
作者
Chan, Yi-Hao [1 ,2 ]
Young, Barnaby E. [3 ,4 ,5 ]
Fong, Siew-Wai [1 ,2 ]
Ding, Ying [3 ]
Goh, Yun Shan [1 ,2 ]
Chee, Rhonda Sin-Ling [1 ,2 ]
Tan, Seow-Yen [6 ]
Kalimuddin, Shirin [7 ,8 ]
Tambyah, Paul A. [9 ]
Leo, Yee-Sin [3 ,4 ,5 ,10 ,11 ,12 ]
Ng, Lisa F. P. [1 ,2 ,13 ,14 ]
Lye, David Chien [3 ,4 ,5 ,11 ,12 ]
Renia, Laurent [1 ,2 ]
机构
[1] Agcy Sci Technol & Res, ASTAR ID Labs, ASTAR Infect Dis Labs, Singapore, Singapore
[2] Agcy Sci Technol & Res, Singapore Immunol Network, Singapore, Singapore
[3] Natl Ctr Infect Dis, Singapore, Singapore
[4] Tan Tock Seng Hosp, Dept Infect Dis, Singapore, Singapore
[5] Nanyang Technol Univ, Lee Kong Chian Sch Med, Singapore, Singapore
[6] Changi Gen Hosp, Dept Infect Dis, Singapore, Singapore
[7] Singapore Gen Hosp, Dept Infect Dis, Singapore, Singapore
[8] Duke NUS Med Sch, Emerging Infect Dis Program, Singapore, Singapore
[9] Natl Univ Singapore Hosp, Dept Med, Singapore, Singapore
[10] Natl Univ Singapore, Saw Swee Hock Sch Publ Hlth, Singapore, Singapore
[11] Natl Univ Hlth Syst, Singapore, Singapore
[12] Natl Univ Singapore, Yong Loo Lin Sch Med, Singapore, Singapore
[13] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Biochem, Singapore, Singapore
[14] Univ Liverpool, Inst Infect Vet & Ecol Sci, Liverpool, Merseyside, England
来源
FRONTIERS IN IMMUNOLOGY | 2021年 / 12卷
基金
新加坡国家研究基金会; 英国医学研究理事会;
关键词
COVID-19; remdesivir (GS-5734); T-cells; tissue repair; disease progression;
D O I
10.3389/fimmu.2021.680188
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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-gamma. 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.
引用
收藏
页数:10
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