Single-cell analysis of two severe COVID-19 patients reveals a monocyte-associated and tocilizumab-responding cytokine storm.
Chuang GuoBin LiHuan MaXiaofang WangPengfei CaiQiaoni YuLin ZhuLiying JinChen JiangJingwen FangQian LiuDandan ZongWen ZhangYichen LuKun LiXuyuan GaoBinqing FuLianxin LiuXiaoling MaJianping WengHaiming WeiTeng-Chuan JinJun LinKun QuPublished in: Nature communications (2020)
Several studies show that the immunosuppressive drugs targeting the interleukin-6 (IL-6) receptor, including tocilizumab, ameliorate lethal inflammatory responses in COVID-19 patients infected with SARS-CoV-2. Here, by employing single-cell analysis of the immune cell composition of two severe-stage COVID-19 patients prior to and following tocilizumab-induced remission, we identify a monocyte subpopulation that contributes to the inflammatory cytokine storms. Furthermore, although tocilizumab treatment attenuates the inflammation, immune cells, including plasma B cells and CD8+ T cells, still exhibit robust humoral and cellular antiviral immune responses. Thus, in addition to providing a high-dimensional dataset on the immune cell distribution at multiple stages of the COVID-19, our work also provides insights into the therapeutic effects of tocilizumab, and identifies potential target cell populations for treating COVID-19-related cytokine storms.
Keyphrases
- sars cov
- rheumatoid arthritis
- single cell
- juvenile idiopathic arthritis
- rheumatoid arthritis patients
- immune response
- disease activity
- respiratory syndrome coronavirus
- rna seq
- dendritic cells
- drug induced
- oxidative stress
- coronavirus disease
- high throughput
- early onset
- endothelial cells
- systemic lupus erythematosus
- genome wide
- toll like receptor
- stem cells
- high glucose
- ulcerative colitis
- cell therapy
- binding protein
- genetic diversity