医学
免疫疗法
免疫系统
不利影响
免疫抑制
髓样
癌症
临床试验
免疫学
癌症免疫疗法
药理学
内科学
作者
Cathrin Gudd,Lucia Possamai
出处
期刊:Cancers
[Multidisciplinary Digital Publishing Institute]
日期:2022-04-10
卷期号:14 (8): 1913-1913
被引量:14
标识
DOI:10.3390/cancers14081913
摘要
Drug-related hepatotoxicity is an emerging clinical challenge with the widening use of immunotherapeutic agents in the field of oncology. This is an important complication to consider as more immune oncological targets are being identified to show promising results in clinical trials. The application of these therapeutics may be complicated by the development of immune-related adverse events (irAEs), a serious limitation often requiring high-dose immunosuppression and discontinuation of cancer therapy. Hepatoxicity presents one of the most frequently encountered irAEs and a better understanding of the underlying mechanism is crucial for the development of alternative therapeutic interventions. As a novel drug side effect, the immunopathogenesis of the condition is not completely understood. In the liver, myeloid cells play a central role in the maintenance of homeostasis and promotion of inflammation. Recent research has identified myeloid cells to be associated with hepatic adverse events of various immune modulatory monoclonal antibodies. In this review article, we provide an overview of the role of myeloid cells in the immune pathogenesis during hepatoxicity related to cancer immunotherapies and highlight potential treatment options.
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