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免疫相互作用在派姆单抗(PD-1 抑制剂)癌症治疗和心血管并发症中的作用。

Immune interactions in pembrolizumab (PD-1 inhibitor) cancer therapy and cardiovascular complications.

机构信息

Division of Metabolic and Cardiovascular Sciences, Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, Florida, United States.

出版信息

Am J Physiol Heart Circ Physiol. 2023 Oct 1;325(4):H751-H767. doi: 10.1152/ajpheart.00378.2023. Epub 2023 Aug 18.

DOI:10.1152/ajpheart.00378.2023
PMID:37594487
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10659324/
Abstract

The use of immunotherapies like pembrolizumab (PEM) is increasingly common for the management of numerous cancer types. The use of PEM to bolster T-cell response against tumor growth is well documented. However, the interactions PEM has on other immune cells to facilitate tumor regression and clearance is unknown and warrants further investigation. In this review, we present literature findings that have reported the interactions of PEM in stimulating innate and adaptive immune cells, which enhance cytotoxic phenotypes. This triggers secretion of cytokines and chemokines, which have both beneficial and detrimental effects. We also describe how this leads to the development of rare but underreported occurrence of PEM-induced immune-related cardiovascular complications that arise suddenly and progress rapidly to debilitating and fatal consequences. This review encourages further research and investigation of PEM-induced cardiovascular complications and other immune cell interactions in patients with cancer. As PEM therapy in treating cancer types is expanding, we expect that this review will inform health care professionals of diverse specializations of medicine like dermatology (melanoma skin cancers), ophthalmology (eye cancers), and pathology (hematological malignancies) about PEM-induced cardiac complications.

摘要

免疫疗法的应用越来越普遍,如 pembrolizumab(PEM),用于治疗多种癌症类型。PEM 被广泛用于增强 T 细胞对肿瘤生长的反应。然而,PEM 对其他免疫细胞的作用,以促进肿瘤消退和清除尚不清楚,值得进一步研究。在这篇综述中,我们介绍了文献中报道的 PEM 刺激先天和适应性免疫细胞的相互作用,这些相互作用增强了细胞毒性表型。这会触发细胞因子和趋化因子的分泌,这些因子既有有益的,也有有害的作用。我们还描述了这如何导致 PEM 诱导的免疫相关心血管并发症的罕见但报告不足的发生,这些并发症突然发生并迅速发展为使人衰弱和致命的后果。这篇综述鼓励进一步研究和调查 PEM 诱导的心血管并发症和癌症患者中其他免疫细胞的相互作用。随着 PEM 疗法在治疗癌症类型方面的扩展,我们预计这篇综述将使皮肤科(黑色素瘤皮肤癌)、眼科(眼癌)和病理学(血液恶性肿瘤)等医学领域的各种专业的医疗保健专业人员了解 PEM 诱导的心脏并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4c2/10659324/8865c59b9e81/h-00378-2023r01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4c2/10659324/8865c59b9e81/h-00378-2023r01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4c2/10659324/8865c59b9e81/h-00378-2023r01.jpg

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Front Immunol. 2023 May 11;14:1174138. doi: 10.3389/fimmu.2023.1174138. eCollection 2023.
2
Molecular principles of tissue invasion and metastasis.组织侵袭和转移的分子原理。
Am J Physiol Cell Physiol. 2023 May 1;324(5):C971-C991. doi: 10.1152/ajpcell.00348.2022. Epub 2023 Mar 20.
3
CC Chemokine Receptor 4 (CCR4) as a Possible New Target for Therapy.CC 趋化因子受体 4(CCR4)作为一种可能的新治疗靶点。
The role of immune checkpoints PD-1 and CTLA-4 in cardiovascular complications leading to heart failure.
免疫检查点蛋白PD-1和CTLA-4在导致心力衰竭的心血管并发症中的作用。
Front Immunol. 2025 Apr 4;16:1561968. doi: 10.3389/fimmu.2025.1561968. eCollection 2025.
4
From Bench to Bedside: Translational Approaches to Cardiotoxicity in Breast Cancer, Lung Cancer, and Lymphoma Therapies.从 bench 到 bedside:乳腺癌、肺癌和淋巴瘤治疗中心脏毒性的转化研究方法
Cancers (Basel). 2025 Mar 21;17(7):1059. doi: 10.3390/cancers17071059.
5
Exosome-mediated communication between gastric cancer cells and macrophages: implications for tumor microenvironment.外泌体介导的胃癌细胞与巨噬细胞间通讯:对肿瘤微环境的影响。
Front Immunol. 2024 Feb 22;15:1327281. doi: 10.3389/fimmu.2024.1327281. eCollection 2024.
Int J Mol Sci. 2022 Dec 9;23(24):15638. doi: 10.3390/ijms232415638.
4
CD160 receptor in CLL: Current state and future avenues.慢性淋巴细胞白血病中 CD160 受体:现状与未来研究方向。
Front Immunol. 2022 Nov 7;13:1028013. doi: 10.3389/fimmu.2022.1028013. eCollection 2022.
5
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6
Characterization of immune checkpoint inhibitor-induced cardiotoxicity reveals interleukin-17A as a driver of cardiac dysfunction after anti-PD-1 treatment.免疫检查点抑制剂诱导的心脏毒性的特征分析揭示了白细胞介素-17A 是抗 PD-1 治疗后心脏功能障碍的驱动因素。
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7
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8
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Front Oncol. 2022 Sep 16;12:940127. doi: 10.3389/fonc.2022.940127. eCollection 2022.
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Mitochondrial oxidative stress in the tumor microenvironment and cancer immunoescape: foe or friend?肿瘤微环境中的线粒体氧化应激与癌症免疫逃逸:敌是友?
J Biomed Sci. 2022 Sep 26;29(1):74. doi: 10.1186/s12929-022-00859-2.
10
Emerging mitochondrial signaling mechanisms in cardio-oncology: beyond oxidative stress.在心脏肿瘤学中新兴的线粒体信号机制:超越氧化应激。
Am J Physiol Heart Circ Physiol. 2022 Oct 1;323(4):H702-H720. doi: 10.1152/ajpheart.00231.2022. Epub 2022 Aug 5.