Wendlinger Simone, Wohlfarth Jonas, Kreft Sophia, Siedel Claudia, Kilian Teresa, Dischinger Ulrich, Heppt Markus V, Wistuba-Hamprecht Kilian, Meier Friedegund, Goebeler Matthias, Schadendorf Dirk, Gesierich Anja, Kosnopfel Corinna, Schilling Bastian
Department of Dermatology, University Hospital Würzburg, 97080 Würzburg, Germany.
Department of Dermatology, University Hospital, University of Duisburg-Essen and German Cancer Consortium, Partner Site Essen, 45147 Essen, Germany.
Cancers (Basel). 2022 May 4;14(9):2294. doi: 10.3390/cancers14092294.
Eosinophils appear to contribute to the efficacy of immunotherapy and their frequency was suggested as a predictive biomarker. Whether this observation could be transferred to patients treated with targeted therapy remains unknown.
Blood and serum samples of healthy controls and 216 patients with advanced melanoma were prospectively and retrospectively collected. Freshly isolated eosinophils were phenotypically characterized by flow cytometry and co-cultured in vitro with melanoma cells to assess cytotoxicity. Soluble serum markers and peripheral blood counts were used for correlative studies.
Eosinophil-mediated cytotoxicity towards melanoma cells, as well as phenotypic characteristics, were similar when comparing healthy donors and patients. However, high relative pre-treatment eosinophil counts were significantly associated with response to MAPKi ( = 0.013). Eosinophil-mediated cytotoxicity towards melanoma cells is dose-dependent and requires proximity of eosinophils and their target in vitro. Treatment with targeted therapy in the presence of eosinophils results in an additive tumoricidal effect. Additionally, melanoma cells affected eosinophil phenotype upon co-culture.
High pre-treatment eosinophil counts in advanced melanoma patients were associated with a significantly improved response to MAPKi. Functionally, eosinophils show potent cytotoxicity towards melanoma cells, which can be reinforced by MAPKi. Further studies are needed to unravel the molecular mechanisms of our observations.
嗜酸性粒细胞似乎有助于免疫治疗的疗效,其数量被认为是一种预测性生物标志物。这种观察结果是否能推广到接受靶向治疗的患者中仍不清楚。
前瞻性和回顾性收集了健康对照者和216例晚期黑色素瘤患者的血液和血清样本。通过流式细胞术对新鲜分离的嗜酸性粒细胞进行表型特征分析,并在体外与黑色素瘤细胞共培养以评估细胞毒性。使用可溶性血清标志物和外周血细胞计数进行相关性研究。
比较健康供体和患者时,嗜酸性粒细胞介导的对黑色素瘤细胞的细胞毒性以及表型特征相似。然而,治疗前较高的嗜酸性粒细胞相对计数与对MAPKi的反应显著相关( = 0.013)。嗜酸性粒细胞介导的对黑色素瘤细胞的细胞毒性是剂量依赖性的,并且在体外需要嗜酸性粒细胞与其靶标接近。在嗜酸性粒细胞存在的情况下进行靶向治疗会产生附加的杀肿瘤作用。此外,共培养时黑色素瘤细胞会影响嗜酸性粒细胞的表型。
晚期黑色素瘤患者治疗前较高的嗜酸性粒细胞计数与对MAPKi的反应显著改善相关。在功能上,嗜酸性粒细胞对黑色素瘤细胞显示出强大的细胞毒性,这可以通过MAPKi增强。需要进一步研究来阐明我们观察结果的分子机制。