免疫检查点抑制剂诱导心肌炎的分子病理学研究

Krystal Hughes
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引用次数: 1

摘要

许多临床试验的结果支持与使用免疫检查点抑制剂(ICIs)相关的肿瘤预后的改善。尽管大多数报告这些药物临床疗效的出版物包括对生物学机制的讨论,但与适应性免疫反应的复杂性有关的叙述经常是,尽管它们不应该是平凡的。同样明显的是,在绝大多数报道与ICI治疗相关的不良事件的论文中,对毒性反应的病理机制的解释往往是粗略的,甚至是完全缺乏的。此外,认为细胞毒性CD8 + T细胞不仅介导抗肿瘤,而且介导免疫相关的不良反应可能是合理的,但不正确。在这种情况下,作者选择仔细研究T细胞在心肌炎发病机制中的作用,而不是仅仅提供与黑色素瘤患者联合ICI治疗相关的严重不良事件的临床细节,作为其他ICI相关自身免疫事件的一个例子。
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Molecular Pathology of Immune Checkpoint Inhibitor-Induced Myocarditis
: The improvement in tumor outcomes associated with the use of immune checkpoint inhibitors (ICIs) is supported by results of numerous clinical trials. Even though most publications reporting the clinical efficacy of these agents include a discussion of the biological mechanisms, narratives related to the complex nature of the adaptive immune response are frequently, though they should not be, mundane. It is also apparent that there tends to be a cursory, or even complete absence, of explanations related to the pathological mechanism(s) of the toxic reactions in the vast majority of papers that report adverse events associated with ICI therapy. Furthermore, the belief that cytotoxic CD8 + T cells mediate not only the antitumor, but also immune-related adverse, effects may be plausible, yet incorrect. This being the case, instead of providing only clinical details of a severe adverse event associated with combination ICI therapy in a patient with melanoma, the authors chose to scrutinize the repertoire and role of T cells in the pathogenesis of myocarditis as an example of other ICI-associated incidents of autoimmunity.
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