Johansson Angelica, Kalliara Eirini, Belfrage Emma, Alling Teodor, Pyl Paul Theodor, Gerdtsson Anna Sandström, Gullberg Urban, Porwit Anna, Drott Kristina, Ek Sara
Department of Immunotechnology, Faculty of Engineering (LTH), Lund University, 223 63 Lund, Sweden.
Department of Dermatology and Venereology, Skane University Hospital (SUS), 205 02 Lund, Sweden.
Biomedicines. 2025 Jan 14;13(1):186. doi: 10.3390/biomedicines13010186.
Mycosis fungoides (MF) is a rare malignancy, with an indolent course in the early stages of the disease. However, due to major molecular and clinical heterogeneity, patients at an advanced stage of the disease have variable responses to treatment and considerably reduced life expectancy. Today, there is a lack of specific markers for the progression from early to advanced stages of the disease. To address these challenges, the non-interventional BIO-MUSE trial was initiated. Here, we report on a case study involving one patient, where combined omics analysis of tissue and blood was used to reveal the unique molecular features associated with the progression of the disease. We applied 10× genomics-based single-cell RNA sequencing to CD3+ peripheral T-cells, combined with T-cell receptor sequencing, to samples collected at multiple timepoints during the progression of the disease. In addition, GeoMx-based digital spatial profiling of T-helper (CD3+/CD8-), T-cytotoxic (CD3+/CD8+), and CD163+ cells was performed on skin biopsies. The results pinpoint targets, such as transforming growth factor β1, as some of the mechanisms underlying disease progression, which may have the potential to improve patient prognostication and the development of precision medicine efforts. We propose that in patients with MF, the evolution of the malignant clone and the associated immune response need to be studied jointly to define relevant strategies for intervention.
蕈样肉芽肿(MF)是一种罕见的恶性肿瘤,在疾病早期病程较为缓慢。然而,由于主要的分子和临床异质性,疾病晚期患者对治疗的反应各不相同,预期寿命也大幅缩短。目前,缺乏用于疾病从早期进展到晚期的特异性标志物。为应对这些挑战,启动了非干预性的BIO-MUSE试验。在此,我们报告一项涉及一名患者的案例研究,其中利用组织和血液的多组学分析来揭示与疾病进展相关的独特分子特征。我们对疾病进展过程中多个时间点采集的样本,将基于10×基因组学的单细胞RNA测序应用于CD3 +外周T细胞,并结合T细胞受体测序。此外,对皮肤活检样本进行了基于GeoMx的辅助性T细胞(CD3 + / CD8 -)、细胞毒性T细胞(CD3 + / CD8 +)和CD163 +细胞的数字空间分析。结果确定了诸如转化生长因子β1等靶点,作为疾病进展的一些潜在机制,这可能有助于改善患者预后并推动精准医学的发展。我们建议,对于MF患者,需要联合研究恶性克隆的演变及相关免疫反应,以确定相关的干预策略。