托珠单抗
细胞激素风暴
细胞因子释放综合征
细胞因子
医学
白细胞介素6
免疫学
受体
细胞因子受体
糖蛋白130
MAPK/ERK通路
单克隆抗体
2019年冠状病毒病(COVID-19)
信号转导
疾病
内科学
抗体
生物
细胞生物学
类风湿性关节炎
传染病(医学专业)
作者
Abinit Saha,Ashish Ranjan Sharma,Manojit Bhattacharya,Garima Sharma,Sang Soo Lee,Chiranjib Chakraborty
标识
DOI:10.1016/j.arcmed.2020.05.009
摘要
Presently, we need more therapeutic molecules for this COVID-19 outbreak. The severity and mortality of the disease is associated with a high level of release of cytokine in the patients which is known as CRS (cytokine release syndrome) or cytokine storm syndrome. IL-6 is a type of pro-inflammatory cytokine which release in the severe COVID-19 patients. This cytokine initiates CRS the JAK-STAT or MAPK/NF-κB-IL-6 pathway. Tocilizumab, a humanized monoclonal antibody, is designed to bind both mIL-6R (membrane bound receptor for IL-6) and sIL-6R (soluble receptor for IL-6) and inhibit the JAK-STAT or MAPK/NF-κB-IL-6 signaling pathway. It finally stops the cytokine storm syndrome. However, we need to understand that how tocilizumab is bound with mIL-6R or sIL-6R. Similarly, we also need to understand more about the real molecular mechanism of activity of tocilizumab.
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