嗜酸性粒细胞和黑色素瘤:免疫治疗的意义

IF 3.9 3区 医学 Q2 CELL BIOLOGY
India Robinson, Gabriella Santa Lucia, Andraia Li, Nathaniel Oberholtzer, John Plante, Kristen M. Quinn, Daniel Reuben, Shikhar Mehrotra, Manuel Valdebran
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引用次数: 3

摘要

免疫检查点阻断剂(ICB)等新疗法延长了晚期黑色素瘤患者的生存期。然而,ICBs已经证明对关节、肝脏、肺、皮肤和肠道有衰弱的副作用。已经确定了几种生物标志物在预测哪些患者更好地耐受ICBs方面的作用。尽管如此,这些生物标志物受到免疫和遗传异质性以及转化为临床实践的复杂性的限制。最近的观察性研究表明,嗜酸性粒细胞计数和血清嗜酸性粒细胞阳离子蛋白水平与晚期黑色素瘤患者的生存期延长显著相关。因此,嗜酸性粒细胞很可能通过尚未探索的机制调节治疗反应。在这里,我们回顾了嗜酸性粒细胞的功能,它们在黑色素瘤中的致癌作用,并讨论了这些机制如何影响患者对ICBs的反应及其在临床实践中的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Eosinophils and melanoma: Implications for immunotherapy
New therapies such as immune checkpoint blockers (ICB) have offered extended survival to patients affected by advanced melanoma. However, ICBs have demonstrated debilitating side effects on the joints, liver, lungs, skin, and gut. Several biomarkers have been identified for their role in predicting which patients better tolerate ICBs. Still, these biomarkers are limited by immunologic and genetic heterogeneity and the complexity of translation into clinical practice. Recent observational studies have suggested eosinophil counts, and serum levels of eosinophil cationic protein are significantly associated with prolonged survival in advanced‐stage melanoma. It is likely that eosinophils thereby modulate treatment response through mechanisms yet to be explored. Here, we review the functionality of eosinophils, their oncogenic role in melanoma and discuss how these mechanisms may influence patient response to ICBs and their implications in clinical practice.
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来源期刊
Pigment Cell & Melanoma Research
Pigment Cell & Melanoma Research 医学-皮肤病学
CiteScore
8.90
自引率
2.30%
发文量
54
审稿时长
6-12 weeks
期刊介绍: Pigment Cell & Melanoma Researchpublishes manuscripts on all aspects of pigment cells including development, cell and molecular biology, genetics, diseases of pigment cells including melanoma. Papers that provide insights into the causes and progression of melanoma including the process of metastasis and invasion, proliferation, senescence, apoptosis or gene regulation are especially welcome, as are papers that use the melanocyte system to answer questions of general biological relevance. Papers that are purely descriptive or make only minor advances to our knowledge of pigment cells or melanoma in particular are not suitable for this journal. Keywords Pigment Cell & Melanoma Research, cell biology, melatonin, biochemistry, chemistry, comparative biology, dermatology, developmental biology, genetics, hormones, intracellular signalling, melanoma, molecular biology, ocular and extracutaneous melanin, pharmacology, photobiology, physics, pigmentary disorders
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