Immune-related adverse events of biological immunotherapies used in COVID-19

被引:1
|
作者
Baracaldo-Santamaria, Daniela [1 ]
Barros-Arias, Giovanna Maria [1 ]
Hernandez-Guerrero, Felipe [1 ]
De-La-Torre, Alejandra [2 ]
Calderon-Ospina, Carlos-Alberto [1 ,3 ]
机构
[1] Univ Rosario Bogota, Sch Med & Hlth Sci, Dept Biomed Sci, Pharmacol Unit, Bogota, Colombia
[2] Univ Rosario, Escuela Med & Ciencias Salud, Neurovitae Ctr, Neurosci Res Grp NEUROS, Bogota, Colombia
[3] Univ Rosario, Escuela Med & Ciencias Salud, Ctr Res Genet & Genom CIGGUR, Bogota, Colombia
关键词
COVID-19; monoclonal abs; tocilizumab; sarilumab; siltuximab; sotrovimab; adverse reactions; TOCILIZUMAB MONOTHERAPY; DOUBLE-BLIND; PATIENT; ARTHRITIS; SAFETY; NEUTROPENIA; DISEASE; DESENSITIZATION; IMMUNOGENICITY; INHIBITION;
D O I
10.3389/fphar.2022.973246
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The use of biological immunotherapeutic drugs is one of the options currently being evaluated and employed to manage COVID-19, specifically monoclonal antibodies, which have shown benefit by regulating the excessive immune response seen in patients with severe infection, known as a cytokine storm. Tocilizumab has received particular importance for this clinical application, as has sarilumab. Both drugs share a substantial similarity in terms of pharmacodynamics, being inhibitors of the interleukin six receptor (IL-6R alpha). Furthermore, sotrovimab, a neutralizing anti-SARS CoV-2 antibody, has gained the attention of the scientific community since it has recently been authorized under certain circumstances, positioning itself as a new therapeutic alternative in development. However, despite their clinical benefit, biological immunotherapies have the potential to generate life-threatening immune-related adverse events. Therefore it is essential to review their incidence, mechanism, and risk factors. This review aims to provide a comprehensive understanding of the safety of the biological immunotherapeutic drugs currently recommended for the treatment of COVID-19, provide a review of the known immune-mediated adverse events and explore the potential immune-related mechanisms of other adverse reactions.
引用
收藏
页数:12
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